Accueil / Annexes / Téléchargements
Téléchargements
Bienvenue dans la section "Téléchargements" de notre site internet.
Le site de la DEQM contient un certain nombre de fichiers et de formulaires, qui peuvent être téléchargés à l'aide de Microsoft Word (DOC) ou Adobe PDF (Portable Document Format). Pour accéder aux fichiers PDF, vous devez avoir une copie d'Acrobat Reader sur votre ordinateur, qui est disponible gratuitement sur le site d'Adobe (voir http://www.adobe.com). Pour ouvrir un document, il suffit de cliquer sur le lien correspondant et attendre que votre ordinateur ait téléchargé le document.
Note: L'adresse e-mail se termine "@edqm.eu" (remplace le "@ pheur.org"). L'adresse e-mail "info@edqm.eu" n'est plus valide. Pour contacter la DEQM, merci d'utiliser le HelpDesk de la DEQM.
Archives de Pharmeuropa et de Pharmeuropa Bio & Scientific Notes
- Pour consulter les archives de Pharmeuropa, voir Archives de Pharmeuropa.
- Pour consulter les archives de Pharmeuropa Bio & Scientific Notes, Voir Pharmeuropa Bio & Scientific Notes.
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- EDQM HealthCare European Pharmacopoeia & PDG Certification OMCL Activities & Guidelines Publications, Products Events organised by the EDQM HelpDesk Other Spécifiques
- Plan d\'accès
- Photo promotion du don d\'organes 2011
octobre 2011 - Presentation material
- General
- EDQM Brochure
- Brochure de la DEQM (mise à jour : juin 2010)
Présentation de la DEQM - Brochure de la DEQM (mise à jour : juillet 2011)
Présentation de la DEQM
- Brochure de la DEQM (mise à jour : juin 2010)
- Annual Report of Activities
- Rapport Annuel d\'activités de la DEQM 2010
- Rapport Annuel d\'activités de la DEQM 2009
- Rapport Annuel d\'activités 2008
- Rapport Annuel d\'activités 2007
- Rapport Annuel d\'activités 2006
- Rapport Annuel d\'activités 2005
- Rapport Annuel d\'activités 2004
- Rapport Annuel d\'activités 2003
- Rapport Annuel d\'activités 2002
- Rapport Annuel d\'activités 2001
- Corrigendum - Annual Report Activities 2001 - Biological Standardisation
- Rapport Annuel d\'activités 2000
- Rapport Annuel d\'activités 1999
- Press releases
- Latest issue
- Press archives
- 2012
- 2011
- 140eme session Pharmacopée européenne
- GDP Reunion, 14-15 juin 2011
- CP Sympo Alt Animal Septembre Fr
- Assemblée Annuelle du Réseau Européen des OMCL
- Réunion annuelle des autorités nationales de pharmacopée
- Congrès de l\'ISBT et Guide TS
- 139eme session Pharmacopée européenne
- Symposium consacré à la lutte contre les médicaments contrefaits
- La DEQM étend la certification ISO 9001
- La DEQM developpe une version de demonstration de Track and Trace
- Reunion du Comite d\'experts sur la Classification des medicaments
- Nouvelle édition du Guide sur la sécurité et l\'assurance de qualité de la transplantation d\'organes, de tissus et de cellules
- Nouvelle collaboration avec les autorités chinoises
- CP Black Sea Meeting
- Nouvelle page web sur les Projets de transfusion sanguine
Nouvelle page web sur les projets de transfusion sanguine - Combattre la contrefaçon de produits médicaux : le Conseil de l’Europe
- Contrefaçon de produits médicaux: douze pays adhèrent à la Convention
- 141eme session Pharmacopée européenne
- Atelier: Classification des médicaments selon leur mode de délivrance, 8-9 novembre 2011
- GDP Reunion, 8-9 novembre 2011
- Communiqués de presse 2011
- 2010
- Convention Medicrime
- La DEQM renforce ses liens de cooperation internationale
- 138ème Session de la Commission européenne de Pharmacopée, Strasbourg
- GDP Reunion, 8-11 novembre 2010
- Conference internationale_mondialisation_et_qualite_des_medicaments
- CV et photo M. Ek
- 137ème Session de la Commission européenne de Pharmacopée
- GDP Réunion, 7-10 juin 2010
- OMCL Assemblée Annuelle, 17-21 mai 2010
15th Annual Meeting of European Network of Official Medicines Control Laboratories (OMCL), Split, Croatia, 17-21 May 2010 - Réunion annuelle des Autorités Nationales de Pharmacopée, 10-11 mai 2010
- Announce d\'une nouvelle collaboration entre la DEQM et l\'OMS
- La Conferencia Internacional sobre la falsificación de productos médicos, 15-16 de abril, Basilea, Suiza
- La conférence internationale sur la contrefaçon de produits, 15-16 avril, Bale, Suisse
- 136e Session de la Commission européenne de Pharmacopée, Strasbourg
- Formation Lisbon contre la contrefaçon des médicaments
- La DEQM reçoit la Certification ISO 9001:2008
- Communiqués de presse 2010
- 2009
- 135ème Session de la Commission européenne de Pharmacopée, Strasbourg
- La DEQM poursuit ses inspections en Chine
- GDP Réunion, 26-29 octobre 2009
Groupe de Discussion des Pharmacopées (GDP), St Louis, Missouri, USA, 26-29 octobre 2009 - CP EODD
- DSO Press Release 11th EODD (German version)
- DSO Press Release 11th EODD
- 134th Session of the European Pharmacopoeia Commission, Strasbourg
- 134e session de la Commission Européenne de Pharmacopée, Strasbourg
- World Blood Donor Day
- Journée Mondiale du donneur de sang
- PDG Meeting, 7-11 June 2009
Pharmacopoeial Discussion Group (PDG) meeting, Yokohama, Japan, 7-11 June 2009 - GDP Réunion, 7-11 juin 2009
Groupe de Discussion des Pharmacopées (GDP), Yokohama, Japon, 7-11 juin 2009 - OMCL Annual Seminar, 25-29 May 2009
14th Annual Meeting of European Network of Official Medicines Control Laboratories (OMCL), Vienna, Austria, 25-29 May 2009 - Réunion annuelle des Autorités Nationales de Pharmacopée et de la Pharmacopée Européenne, 11-12 mai
- National Pharmacopoeia Authorities Annual Meeting, 11-12 May
- Assemblée annuelle du Réseau Réseau Européen des Laboratoires OMCL, 25-29 mai 2009
- La DEQM conclut des accords de confidentialite avec l\'US-FDA et la TGA
- Utilisation clinique optimale des composants sanguins, 24-25 avril
- Optimal clinical use of blood components, 24-25 April
International Symposium, 24-25 April 2009, Wilbad Kreuth (Germany) - Appointments April 2009
- Nominations Avril 2009
- 133rd Session of the European Pharmacopoeia Commission Held in Strasbourg
- 133e session de la Commission Européenne de Pharmacopée, Strasbourg
- 2009 Archives presse
- 2008
- Press Releases 2008 Archives (English)
- Communiqués de presse 2008 Archives (Francais)
- Counterfeit medicines, 9 December 2008
Communication empowers the public to participate in minimising health risks - Médicaments de contrefacon, 9 Décembre 2008
La communication renforce la capacité du grand public à participer à la réduction des risques sanitaires - 132ème session de la Commission européenne de Pharmacopée
- 132nd Session PhEur Commission, 28 November 2008
- Counterfeit medicines - Model for a network, 17 March 2008
- PDG Meeting, 10-13 November 2008
Pharmacopoeial Discussion Group (PDG) meeting, Brussels, Belgium, 10-13 November 2008 - GDP Reunion, 10-13 novembre 2008
Groupe de Discussion des Pharmacopées (GDP), Bruxelles, Belgique, 10-13 novembre 2008 - Russian Federation and EDQM
- La Federation de Russie et la DEQM
- Pharmaceutical Reference Substance Press Release
- Etalons de reference pharmaceutique
- 10th European Day for Organ Donation and Transplantation
- 10ème Journée Européenne du don d\'organe et de la greffe
- Rencontre entre la DEQM et des representants du Projet de Pharmacopee Chilienne
- Meeting EDQM & representatives Chilean Pharmacopoeia Project
- 2nd Workshop on the Characterisation of Heparin Products, 19-20 June 2008
- 2eme Atelier sur la caracteristion de produits hepariniques
- Revised heparin monographs adopted
- Les monographies révisées des héparines
- 131st Session PhEur Commission, 27 June 2008
- 131eme Session de la Commission Européenne de Pharmacopée, 27 juin 2008
- Training on best practices to combat counterfeiting, 11 June 2008
- Session de formation sur les meilleures pratiques pour combattre la contrefacon, 11 juin 2008
- OMCL Annual Seminar, 2-6 June 2008
13th Annual Meeting of European Network of Official Medicines Control Laboratories (OMCL), Strasbourg, France, 2-6 June 2008 - Assemblée annuelle du Réseau Réseau Européen des Laboratoires OMCL, 2-6 juin 2008
- PDG Meeting, 1-5 June 2008
Pharmacopoeial Discussion Group (PDG) meeting, Portland, USA, 1-5 June 2008 - GDP Reunion, 1-5 juin 2008
Groupe de Discussion des Pharmacopées (GDP), Portland, Etats-Unis, 1-5 juin 2008 - La DEQM participe à une rencontre internationale sur les héparines, 13 mai 2008
- EDQM saddened by death of Peter Castle, 14 May 2008
- Tristesse de la DEQM à l\'annonce de la Disparition de Peter Castle, 14 mai 2008
- EDQM participates in meeting on heparins, 13 May 2008
- Meeting EDQM & Indian Authorities, 30 April 2008
- Réunion entre la DEQM & les authorités indiennes, 30 avril 2008
- Alternatives to Animal Testing, Dubrovnik, Croatia, 23-24 April 2008
- Remplacement des essais sur animaux, Dubrovnik, Croatie, 23-24 avril 2008
- 130th Session PhEur Commission, 18 March 2008
- 130eme Session de la Commission Européenne de Pharmacopée, 18 mars 2008
- New observer to PhEur, 6 March 2008
- Nouvel observateur PhEur, 6 mars 2008
- New Blood Transfusion Guide, 4 March 2008
- Nouveau Guide Transfusion Sanguine, 4 mars 2008
- EDQM French language website, 11 February 2008
- Version française du site Internet de la DEQM, 11 février 2008
- 2007
- Press Releases 2007 Archives
- PDG Meeting, 28 Oct - 1 Nov 07
Pharmacopoeial Discussion Group (PDG) meeting, Yokohama, Japan, 28 Oct - 1 Nov 2007 - Réunion GDP, 28 Oct-1 Nov 07
- 9th European day Organ Donation & Transplantation
09/10/2007 - EDQM Director appointed
Council of Europe appoints new Director of the EDQM - New Frontiers in the Q of Medicines, Strasbourg, France, 13-15 June 2007
26/07/2007 - European Cooperation & Synergy in QS beyond the European Pharmacopoeia, 15-16 June 2007
- Reference Standards - Agreement with ShFDA & SIFDC
English and Chinese Text - Reference Standards - Agreement with ShFDA & SIFDC
English and Frecnh Text - OMCL Annual Seminar, 7-11 May 07
12ème réunion annuelle du réseau européen des laboratoires officiels de contrôle des médicaments (OMCL), Prague, République Tchèque, 7-11 mai 2007 - PDG Meeting, 7-10 May 07
Pharmacopoeial Discussion Group (PDG) meeting, Brussels, Belgium, 7-10 May 2007 - Meeting of CD-P-TO & Chair elected, 25 April 2007
Meeting of the European Committee on Organ Transplantation & Chair elected - Réunion du CD-P-TO & Président, 25 avril 2007
- National Pharmacopoeia Secretariats, 23-24 April 2007
Annual meeting of national Pharmacopoeia secretariats, 23-24 April 2007, Rijeka, Croatia - Meeting of CD-P-TS & Chair elected, 28 March 2007
Meeting of the European Committee on Blood Transfusion & Chair elected - Réunion du CD-P-TS & Président, 28 mars 2007
- New Chair PhEur Commission, 27 March 2007
Election of the new Chair of the European Pharmacopoeia Commission - CEP - Memo of Understanding
EDQM and HPFB of Health Canada sign Memo of Understanding - Inauguration building, 19 March 2007
Inauguration of the new EDQM building, 19 March 2007 - New observer to PhEur, 20 Feb 2007
The Republic of Belarus - New Name EDQM, Jan 2007
The EDQM has become the EDQM & HealthCare
- 2006
- 2006 Press Releases Archives
- 5th Edition Online version available in Spanish
- EDQM_Team_Visit_China
Multidisciplinary EDQM team on official journey to China, 17-29 June 2006 - PDG Meeting, 23-25 October 2006
Pharmacopoeial Discussion Group (PDG) meeting, Chicago, USA, 23-25 October 2006 - Avian Influenza Symposium, 19-20 Oct 2006
Press Release - Requirements for production and control of avian influenza vaccines, 19-20 October 2006 - Microbiology Symposium, 2-3 Oct 2006
Press Release - New Microbiology Chapters of the European Pharmacopoeia, 2-3 October 2006 - Impurities Symposium, 21-22 Sept 2006
Press Release - Impurities control : setting specifications for antibiotics and peptides, 21-22 September 2006 - New observers, 29 June 2006
The Russian Federation & the Republic of Kazakhstan - PDG Meeting, 5-8 June 2006
Pharmacopoeial Discussion Group (PDG) meeting, Yokohama, Japan, 5-8 June 2006 - OMCL Annual Seminar 9-12 May 2006
11th Annual Meeting of European Network of Official Medicines Control Laboratories (OMCL), Limassol, Cyprus, 9-12 May 2006 - EDQM as a WHO Collaborative Centre, 4 May 2006
EDQM designated as a WHO Collaborative Centre for ISA
- Press articles
- Quality, Safety and Environment
- Quality
- Safety
- Consultation Publique Classification des dangers
Consultation publique au sujet de la mise en application du Système Général Harmonisé de l\'ONU (GHS) relatif à la classification des dangers pour les étalons de référence - Table: EDQM Consultation GHS
NOTE: This document has 183 pages.
- Consultation Publique Classification des dangers
- Environment
- Library
- Visits
- Formulaire de Demande de Visite
EDQM Visit Request Form (Word format)
- Formulaire de Demande de Visite
- Job Opportunities
- HealthCare EDQM European Pharmacopoeia & PDG Certification OMCL Activities & Guidelines Publications, Products Events organised by the EDQM HelpDesk Other Spécifiques
- 1- General
- 2- Blood Transfusion
- General
- Pandemic Influenza - Planning for Blood Organisations
Consolidating the work of the European Blood Alliance Emergency Planning Action Group (EBA EPAG) (May 2009) - Dr Rut Norda - Curriculum Vitae
- Terms of Reference CD-P-TS
- Mandat du comité CD-P-TS
- List of Members - CD-P-TS
- List of Members - List of Members of the ad-hoc Working Group - Blood Transfusion Guide (GTS)
- Informations générales sur les activités de la DEQM liées à la transfusion sanguine (anglais /français, 2011)
- Blood Transfusion Activities Factsheet (English, Jan 2009)
- Activités liées à la Transfusion Sanguine Factsheet (Francais, janvier 2009)
- Pandemic Influenza - Planning for Blood Organisations
- Recommendations
- Transfusion Sanguine Recommandations (téléchargez toutes les recommandations, Français)
- Mémoire explicatif de la Recommandation Rec(2004)18
- Recommandation Rec(2004)18 du Comité des Ministres aux Etats membres relative à l’enseignement de la médecine transfusionnelle au personnel infirmier
- Recommandation Rec(2004)8 du Comité des Ministres aux Etats membres sur les banques de sang de cordon autologue
- Explanatory Memorandum to the Recommendation Rec(2004)8
- Recommandation Rec(2003)11 du Comité des Ministres aux Etats membres sur la mise en place de procédures d’inactivation des agents pathogènes pour les composants sanguins
- Recommandation Rec(2002)11 du Comité des Ministres aux Etats membres sur le rôle de l’hôpital et du clinicien s’agissant de garantir l’usage optimal du sang et des produits sanguins
- Recommandation Rec(2001)4 du Comité des Ministres aux Etats membres sur la prévention du risque de transmission de la forme nouvelle de la maladie de Creutzfeldt-Jakob (vMCJ) par transfusion sanguine
- Recommandation No R(98)10 du Comité des Ministres aux Etats membres sur l\'utilisation de concentrés érythrocytaires humains pour la préparation de transporteurs d\'oxygène
- Recommandation No R(98) 2 du Comité des Ministres aux Etats membres sur la production de progéniteurs hématopoïétiques
- Recommandation No R(96) 11 du Comité des Ministres aux Etats membres sur la documentation et l\'archivage destinés à garantir le suivi du sang et des produits sanguins, notamment dans les hôpitaux
- Recommandation No R(95) 15 du Comité des Ministres aux Etats membres sur la préparation, l\'utilisation et l\'assurance de qualité des composants sanguins
- Recommandation No R(95) 14 du Comité des Ministres aux Etats membres sur la protection de la santé des donneurs et des receveurs dans le cadre de la transfusion sanguine
- Recommandation No R(94) 10 du Comité des Ministres aux Etats membres sur l\'intervention pharmacologique précoce en cas d\'infection par le VIH
- Recommandation No R (93) 4 du Comité des Ministres aux États membres aux essais cliniques nécessitant l\'utilisation de composants et de produits issus du fractionnement du sang et du plasma humains
- Recommandation No R(90) 9 du Comité des Ministres aux Etats membres sur les produits plasmatiques et l\'autosuffisance européenne
- Recommandation No R(90) 3 du Comité des Ministres aux Etats membres sur la recherche médicale sur l\'etre humain
- Recommandation No R(89) 14 du Comité des Ministres aux Etats membres sur les incidences éthiques de l\'infection VIH dans le cadre sanitaire et social
- Recommandation No R(88) 4 du Comité des Ministres aux Etats membres sur les responsabilités sanitaires dans le domaine de la transfusion sanguine
- Recommandation No R(87) 25 du Comité des Ministres aux Etats membres concernant une politique européenne commune de santé publique de lutte contre le syndrome d\'immunodéficience acquise (SIDA)
- Recommandation No R(86) 6 du Comité des Ministres aux Etats membres relative aux lignes directrices pour la préparation, le contrôle de qualité et l\'utilisation du plasma frais congelé (PFC)
- Recommandation No R(85) 12 du Comité des Ministres aux Etats membres sur le dépistage de la présence de marqueurs du SIDA chez les donneurs de sang
- Recommandation No R(85) 5 du Comité des Ministres aux Etats membres relative à un modèle de programme pour la formation des futurs spécialistes en transfusion sanguine
- Recommandation No R(84) 16 du Comité des Ministres aux Etats membres concernant la notification des travaux impliquant de l\'acide désoxyribonucléique (ADN) recombiné
- Recommandation No R(84) 6 du Comité des Ministres aux Etats membres sur la prévention de la transmission du paludisme par la transfusion sanguine
- Recommandation No R(83) 8 du Comité des Ministres aux Etats membres sur la prévention de la transmission possible du syndrome d\'immunodépression acquise (SIDA) des donneurs contaminés aux receveurs de sang ou de produits sanguins
- Recommandation No R(81) 14 du Comité des Ministres aux Etats membres sur la prévention de la transmission de maladies infectieuses dans le transfert international du sang, de ses composants et de ses dérivés
- Recommandation No R(81) 5 du Comité des Ministres aux Etats membres concernant l\'administration prénatale de l\'immunoglobuline anti-D
- Recommandation No R(80) 5 du Comité des Ministres aux Etats membres concernant les produits sanguins pour le traitement des hémophilies
- Recommandation No R(79) 5 du Comité des Ministres aux Etats membres concernant le transport et l\'échange internationaux de substances d\'origine humaine
- Reports
- Techniques de réduction des pathogènes dans les composants sanguins destinés à la transfusion - mise à jour mars 2008
- The Collection, Testing and Use of Blood and Blood Components in Europe - 2008 Report
- The Collection, Testing and Use of Blood and Blood Components in Europe - 2007 Report
- Reporting from Council of Europe member states on the collection, testing and use of blood and blood components in Europe : 2006 Survey
- Reporting from Council of Europe member states on the collection, testing and use of blood and blood components in Europe: The 2003 Survey
- Trends and Observations on the Collection, Testing and Use of Blood Components: 2001-2005 Report
- The Collection, Testing and Use of Blood and Blood Components in Europe - 2006 Report
- Collecte, qualification et utilisation du sang et des composants sanguins en Europe - Rapport 2005
- The Collection, Testing and Use of Blood and Blood Components in Europe - 2004 Report
- La collecte, la qualification et l’utilisation du sang et des composants sanguins en Europe - Rapport 2004
- The Collection, Testing and Use of Blood and Blood Products in Europe in 2003
- The Collection, Testing and Use of Blood and Blood Products in Europe in 2002
- The Collection, Testing and Use of Blood and Blood Components in Europe in 2001
- Implementation of Pathogen Reduction Technologies for Blood Components for Transfusion: Updated Table 2009-2010
- Resolutions
- Résolution CM/Res(2008)5 sur la responsabilité des donneurs et sur la limitation du don du sang et des composants sanguins
Adoptée par le Comité des Ministres le 12 mars 2008, lors de la 1021e réunion des Délégués des Ministres - Resolution CM/Res(2008)5 on donor responsibility and on limitation to donation of blood and blood components
Adopted by the Committee of Ministers on 12 March 2008 at the 1021st meeting of the Ministers’ Deputies - Resolution 68 (32) Establishment in Amsterdam of a European blood bank of rare groups
Adopted by the Ministers Deputies on 31 October 1968
- Résolution CM/Res(2008)5 sur la responsabilité des donneurs et sur la limitation du don du sang et des composants sanguins
- World Blood Donor Day
- Projects
- TS057 Risk Behaviours having an impact on Blood Donor Management
- Mandat du Groupe de Travail Ad Hoc subordonné au CD-P-TS
Terms of Reference of the Working Group (October 2011) - PA/PH/TS (11) 5 2R - Rapport d\'avancement des travaux du Groupe de Travail
Octobre 2011 - Presentation on Final Terms of reference (May 2011)
- Risk behaviours having an impact on blood donor management
Risk behaviours having an impact on blood donor management - PA/PH/TS (11) 28 R EUROPEAN COMMITTEE (PARTIAL AGREEMENT) ON BLOOD TRANSFUSION (CD-P-TS) Technical Memorandum
- Mandat du Groupe de Travail Ad Hoc subordonné au CD-P-TS
- TS057 Risk Behaviours having an impact on Blood Donor Management
- General
- 3- Organ Transplantation
- ALLIANCE-O ERANet Coordination Action
- Workshop Meeting Minutes, Paris, 24 Oct 2007
- White Paper 2004-2007
- Work Packages
- Download all 18 work packages
- Work Package 7: Ethical & Legal Aspects
D7.2 - Position Paper - Work Package 7: Ethical & Legal Aspects
D7.1 - Ethical and legal approaches overview - Work Package 6: Fundamental research linked to organ donation
D6.2 - Proposal of strategies to improve efficiency of fundamental research - Work Package 6: Fundamental research linked to organ donation
D6.1 - State of the Art Review - Work Package 5: Coordination of evaluation of methodologies of transplantation performance
D5.4 - Development of future collaboration - Work Package 5: Coordination of evaluation of methodologies of transplantation performance
D5.3 - Review of simulation tools for exploring the merits of different allocation procedures in terms of their impact on patient or graft survival - Work Package 5: Coordination of evaluation of methodologies of transplantation performance
D5.2 - Proposal for standardised methods to monitor the performance of different transplantation teams and standardised risk factors - Work Package 5: Coordination of evaluation of methodologies of transplantation performance
D5.1 - State of the art of evaluation methodologies - Work Package 4: Increase safety and quality of organ transplantation
D4.4 - Common best practices for organ transplantation quality systems - Work Package 4: Increase safety and quality of organ transplantation
D4.3 - State of the art of quality systems - Work Package 4: Increase safety and quality of organ transplantation
D4.2 - Elaboration of common guideline for organ safety - Work Package 4: Increase safety and quality of organ transplantation
D4.1 - State of the art of safety processes, exchange of best practices - Work Package 3: Organ allocation in Europe
D3.2 - Specification of a common simulation tool for organ allocation - Work Package 3: Organ allocation in Europe
D3.1 - Position paper on best practices for organ allocation in Europe - Work Package 2: Expanding Donor Pool
D2.5 - Proposal for common methods and indicators for donor pool estimation - Work Package 2: Expanding Donor Pool
D2.3 - Position paper on promotion of organ donation - Work Package 2: Expanding Donor Pool
D2.2 - Position paper for expanding the donor pool - Work Package 2: Expanding Donor Pool
D2.1 & D2.4 - State of the art in donor pool estimation
State of the art in expanding the donor pool
- General
- NEW: List of members CD-P-TO 26/01/2012
- Dr. Per Pfeffer - Curriculum Vitae
- Terms Of Reference CD-P-TO
- Mandat Du Comité CD-P-TO
- Conference Programme
New Challenges in Organ Donation: How can we improve? 6-7 November 2007, Madrid, Spain - 40 DONORS PMP PLAN, 23 October, Madrid
PLAN DONACIÓN CUARENTA, 23 de Octubre, Madrid (English & Spanish) - The Declaration of Istanbul
Participants in the International Summit on Transplant Tourism and Organ Trafficking convened by The Transplantation Society and International Society of Nephrology in Istanbul, Turkey, April 30–May 2, 2008 - Activités liées à la transplantation d’organes Factsheet (Français, juin 2011)
- Organ Transplantation Activities Factsheet (Russian, June 2011)
- Activités liées à la transplantation d’organes (English/French, 2011)
- General Information on Organ Transplantation Activities (Eng/Russian, 2011)
- Lancet Commentary - Declaration of Istanbul
- Organ transplants: What are the research options?
Inserm Press Release, Paris 29 March 2009 - DSO Communiqué de Pressé-Anglais
- Newletter transplant project overview september 2011
Project overview
- Recommendations
- Transplantation d\'organes Recommandations (Francais)
- Recommandation Rec(2006)16 du Comité des Ministres aux Etats membres sur les programmes d amélioration de la qualité pour le don d organes
- Recommandation Rec(2006)15 du Comité des Ministres aux Etats membres sur le contexte, les fonctions et les responsabilités d’une organisation nationale de transplantation (ONT)
- Recommandation Rec(2005)11 du Comité des Ministres aux Etats membres sur le rôle et la formation des professionnels du don d’organes (« coordinateurs du prélèvement »)
- Recommandation Rec(2004)19 du Comité des Ministres aux Etats membres relative aux critères exigés pour l\'autorisation des centres de transplantations d\'organes
- Recommandation Rec(2004)7 du Comité des Ministres aux Etats membres sur le trafic d organes
- Recommandation Rec(2004)8 du Comité des Ministres aux Etats membres sur les banques de sang de cordon autologue
- Recommandation Rec(2003)12 du Comité des Ministres aux Etats membres relative aux registres des donneurs d’organes
- Explanatory memorandum to Recommendation Rec(2003)10
- Recommandation Rec(2003)10 du Comité des Ministres aux Etats membres sur la xénotransplantation
- Recommandation Rec(2001) 15 du Comité des Ministres aux Etats membres sur la gestion des listes d\'attente et des délais d\'attente en matière de transplantation d\'organe
- Recommandation No R (97) 16 du Comité des Ministres aux Etats membres sur la transplantation du foie prélevé sur des donneurs vivants apparentés
- Recommandation No R (97) 15 du Comité des Ministres aux Etats membres sur la xénotransplantation
- Recommandation No R (94) 1 du Comité des Ministres aux Etats membres sur les banques de tissus humains
- Reports
- Replies to the questionnaire for member states on organ trafficking
- Organ shortage:current status and strategies for improvement of organ donation - A European consensus document
- Joint Council of Europe/United Nations Study on trafficking in organs, tissues and cells and trafficking in human beings for the purpose of the removal of organs
- Résumé général de l\'Étude conjointe du Conseil de l’Europe et des Nations Unies
- Resolutions
- Resolution CM/Res(2008)6 on transplantation of kidneys from living donors who are not genetically related to the recipient
Adopted by the Committee of Ministers on 26 March 2008 at the 1022nd meeting of the Ministers’ Deputies - Résolution CM/Res(2008)6 sur la transplantation de rein de donneurs vivants qui ne sont pas génétiquement liés au receveur
Adoptée par le Comité de Ministres le 26 mars 2008, lors de la 1022e réunion des Délégués des Ministres - Resolution CM/Res(2008)4 on adult-to-adult living donor liver transplantation
Adopted by the Committee of Ministers on 12 March 2008 at the 1021st meeting of the Ministers Deputies - Résolution CM/Res(2008)4 sur la transplantation de foie de donneurs vivants entre adultes
Adoptée par le Comité de Ministres le 12 mars 2008, lors de la 1021e réunion des Délégués des Ministres - Resolution CM/Res(78) 29 on harmonisation of legislations of member states relating to removal, grafting and transplantation of human substances
Adopted by the Committee of Ministers on 11 May 1978 at the 287th meeting of the Ministers\' Deputies - Résolution CM/Res(78) 29 sur l\'harmonisation des législations des Etats membres relatives aux prélèvements, greffes et transplantations de substances d\'origine humaine
Adoptée par le Comité des Ministres le 11 mai 1978,
lors de la 287e réunion des Délégués des Ministres
- Resolution CM/Res(2008)6 on transplantation of kidneys from living donors who are not genetically related to the recipient
- Publications
- Booklet Rec Res Organ transplantation
- Newsletter Transplant
- Newsletter Transplant Vol. 16, No 1 Sept. 2011
- Newsletter Transplant Vol. 15, No 1 Sept. 2010
- Newsletter Transplant Vol. 14, No 1 Sept. 2009
- Newsletter Transplant Vol. 13, No 1 Sept. 2008
- Newsletter Transplant Vol. 12, No 1 Sept. 2007
- Newsletter Transplant Vol. 11, No 1 Sept. 2006
- Newsletter Transplant Vol. 10, No 1 Sept. 2005
- Newsletter Transplant Vol. 9, No 1 Sept. 2004
- European Day for Organ Donation and Transplantation
- ALLIANCE-O ERANet Coordination Action
- 4- Pharmaceutical & Pharmaceutical Care
- General
- Résolution ResAP(2007)1 sur la classification des médicaments relativement à leurs conditions de délivrance
- Mandat du Comité européen sur les produits et les soins pharmaceutiques CD-P-PH
1101e réunion – 8 décembre 2010 - Mandat du Comité d’experts CD-P-PH/CMED
- Mandat du Comité d’experts CD-P-PH/PC
- Mandat du Comité d’experts CD-P-PH/PHO
- Mandat révisé du Comité CD-P-PH
1017e Réunion 06/02/2008
- Reports
- 1101 Réunion, 8 décembre 2010
Comité européen sur les produits et les soins pharmaceutiques (Accord Partiel) (CD-P-PH) - Rapport abrégé de la 4e réunion (Bruxelles, 15-16 septembre 2010) - 1084 Réunion, 5 mai 2010
Comité européen sur les produits et les soins pharmaceutiques (Accord partiel) (CD-P-PH) –
Rapport abrégé de la 3e réunion (Strasbourg, 26-27 janvier 2010) - 1063 Réunion, 8 juillet 2009
Comité européen sur les produits et les soins pharmaceutiques (Accord partiel) (CD-P-PH) –
Rapport abrégé de la 2e réunion (Bruxelles, 2-3 avril 2009) - 1032 Réunion, 9 juillet 2008
Comité européen sur les produits et les soins pharmaceutiques (Accord partiel) (CD-P-PH) - Rapport abrégé de la 1e réunion (Strasbourg, 2-3 avril 2008)
- 1101 Réunion, 8 décembre 2010
- General
- 5- Counterfeit Medicines
- General
- Notification de contrefaçon de medicament
- Counterfeit Medicinal Product Notification Form
- Déclaration de Moscou
Conférence internationale : L\'Europe contre les médicaments contrefaits, 23-24 octobre 2006 - Moscow Declaration
International Conference - Europe against Counterfeit Medicines, 23-24 October 2006 - Un modele de reseau et de points de contact uniques (PCU)
Groupe ad hoc sur les médicaments contrefaits (P-SP-PH/CMED) - Model for a Network and Single Points of Contacts (SPOCs)
Ad hoc Group on Counterfeit Medicines (P-SP-PH/CMED) - Risk communication model
- Symposium consacré à la lutte contre les médicaments contrefaits et illégaux
Symposium consacré à la lutte contre les médicaments contrefaits et illégaux - Combattre la contrefaçon des produits médicinaux et les infractions similaires
Octobre 2011 - Convention médicrime conclusions de la conférence
- Pays signataires Medicrime
- Medicrime poster
- Programme Conference Combatting Falsified Medical Products
- FS médicaments contrefaits
- Reports
- Resolutions
- General
- 6- Classification of Medicines
- General
- Resolutions
- Résolution ResAP(2007)1 sur la classification des médicaments relativement a leur conditions de delivrance - Edition 2010
Remplaçant la Résolution ResAP(2000)1 relative à la classification des médicaments dont la délivrance est soumise à ordonnance - Résolution ResAP(2007)1 sur la classification des médicaments relativement a leur conditions de delivrance - Edition 2010
Remplaçant la Résolution ResAP(2000)1 relative à la classification des médicaments dont la délivrance est soumise à ordonnance - Résolution ResAP(2007)1 sur la classification des médicaments relativement a leur conditions de delivrance - Edition 2009
Remplaçant la Résolution ResAP(2000)1 relative à la classification des médicaments dont la délivrance est soumise à ordonnance - Resolution ResAP(2007)2 English
Good practices for distributing medicines via mail order - Resolution ResAP(2007)2 French
Bonnes pratiques en matière de distribution des médicaments par correspondance - Resolution AP(2007) 1 English
(superseding Resolution ResAP(2000)1 on the classification of medicines which are obtainable only on medical prescription) and Appendices (2008 Edition) - Resolution AP (2007)1 French
(remplaçant la Résolution ResAP(2000)1 relative à la classification des médicaments dont la délivrance est soumise à ordonnance) et Annexes I, II & III
Edition 2008 - Resolution ResAP (2001)2 English
Pharmacists role in the framework of health security - Resolution ResAP (2001) 2 French
Role du pharmacien dans le cadre de la sécurité sanitaire - Resolution AP (2000) 1 English
on the Classification of medicines which are obtainable only on medical prescription, and Appendices (2006 Edition) - Resolution AP (2000) 1 English
on the Classification of medicines which are obtainable only on medical prescription, and Appendices (2005 Edition) - Resolution AP (2000) 1 English
on the Classification of medicines which are obtainable only on medical prescription, and Appendices (2004 Edition)
- Résolution ResAP(2007)1 sur la classification des médicaments relativement a leur conditions de delivrance - Edition 2010
- 7- Quality and safety standards in pharmaceutical
- Conseil de lEurope Modèle Campagne
- Proceedings: Expert Meeting on Medication Safety, 21-22 November, The Hague
- Report 2006
Creation of a better medication safety culture in Europe: Building up safe medication practices, Expert Group on Safe Medication Practices (P-SP-PH/SAFE) - Abridged Survey Report on Quality and Safety Assurance Standards
- Medicines and the Internet
- Core message of user-oriented guidance (German)
- Core message of user-oriented guidance (Spanish)
- Vente et publicite des medicaments sur internet
Préparé par le Comité d’Experts des Questions Pharmaceutiques, le 13 novembre 2002 - Selling and advertising of medicines on the internet
Prepared by the Committee of Experts on Pharmaceutical Questions, 13 November 2002 - Workshop report - Medicines on the web:risks and benefits
UN Internet Governance Forum (IGF), Sharm El Sheik, 15-18 November 2009
- European Pharmacopoeia & PDG EDQM HealthCare Certification OMCL Activities & Guidelines Publications, Products Events organised by the EDQM HelpDesk Other Spécifiques
- European Pharmacopoeia
- NEW: Invitation to participate in the establishment of somatostatin CRS batch 6
- NOUVEAU: L’immunoglobuline humaine normale pour administration par voie intraveineuse
01/2012:0918 - NOUVEAU : Mise en application rapide de la monographie (09) 18
septembre 2011 - NOUVEAU: Lettre circulaire concernant la mise en application rapide de la version revisée de la monographie 0918
- Héparine calcique (08/2010:0332)
Implementation date: 1st August 2010 - Héparine sodique (08/2010:0333)
Implementation date: 1st August 2010 - NMR test protocol for OSCS determination in API Heparin Sodium and Calcium
- Heparin: a new capillary electrophoresis method
- Héparine: une méthode électrophorèse capillaire
- Nouvelle expression des critères d’acceptation pour l’essai des substances apparentées
Informations générales pour des parties concernées - Recommandations relatives à la présentation des monographies de substances d\'origine humaine ou animale
Novembre 2010 - Mise en application rapide du chapitre général 5.2.8 révisé
- Réduction du risque de transmission des agents des encéphalopathies spongiformes animales par les médicaments à usage humain et vétérinaire
En application: 1er juillet 2011. - PhEur Commission Decisions
- 2011
- 2010
- 2009
- Decisions Ph Eur Comm 122009
- Liste des textes adoptes Commission PhEur, décembre 2009
- Decisions Ph Eur Comm 062009
- List of texts adopted at PhEur Commission June 2009
- Liste des textes adoptes Commission PhEur, juin 2009
- Decisions Ph Eur Comm 032009
- List of texts adopted at PhEur Commission March 2009
- Décisions Ph Eur Comm 122009 (Français)
- 2008
- Decisions Ph Eur Comm 112008 (English)
- Décisions Ph Eur Comm 112008 (Français)
- Decisions Ph Eur Comm 062008 (English)
List of new or revised texts adopted by the PhEur Commission, June 2008 session - Décisions Ph Eur Comm 062008 (Francais)
Liste des textes adoptés à la session de juin 2008 de la Commission Européenne de Pharmacopée - Decisions Ph Eur Comm 032008 (English)
List of new or revised texts adopted by the PhEur Commission, March 2008 session - Décisions Ph Eur Comm 032008 (Francais)
Liste des textes adoptés à la session de novembre 2007 de la Commission Européenne de Pharmacopée
- 2007
- Decisions Ph Eur Comm 112007 (English)
List of new or revised texts adopted by the PhEur Commission, June 2007 session - Décisions Ph Eur Comm 112007 (Francais)
Liste des textes adoptés à la session de novembre 2007 de la Commission Européenne de Pharmacopée - Decisions Ph Eur Comm 062007
List of new or revised texts adopted by the PhEur Commission, June 2007 session - Decisions Ph Eur Comm 032007
List of new or revised texts adopted by the PhEur Commission, March 2007 session
- Decisions Ph Eur Comm 112007 (English)
- 2006
- Decisions Ph Eur Comm 112006
List of new or revised texts adopted by the PhEur Commission, November 2006 session - Decisions Ph Eur Comm 062006
List of new or revised texts adopted by the PhEur Commission, June 2006 session - Decisions Ph Eur Comm 032006
List of new or revised texts adopted by the PhEur Commission, March 2006 session
- Decisions Ph Eur Comm 112006
- 2005
- Decisions Ph Eur Com 062005
List of new or revised texts adopted by the PhEur Commission, June 2005 session - Decisions Ph Eur Com 112005
Decisions of the European Pharmacopoeia Commission, November 2005 (texts and CRS/BRP adopted and revisions of monographs and general texts) - Decisions Ph Eur Com 032005
Decisions of the European Pharmacopoeia Commission, March 2005 (texts and CRS/BRP adopted and revisions of monographs and general texts)
- Decisions Ph Eur Com 062005
- 2004
- Decisions Ph Eur Com 062004
Decisions of the European Pharmacopoeia Commission, June 2004 (texts and CRS/BRP adopted and revision of monographs and general texts). - Decisions Ph Eur Com 112004
Decisions of the European Pharmacopoeia Commission, November 2004 (texts and CRS/BRP adopted and revisions of monographs and general texts).
- Decisions Ph Eur Com 062004
- 2003
- Decisions Ph Eur Com 112003
Decisions of the European Pharmacopoeia Commission, November 2003 (texts and CRS/BRP adopted and revision of monographs and general texts).
- Decisions Ph Eur Com 112003
- Work Programme
- 2011
- Mise à jour Programme de travail mars 2011
- Mise à jour du Programme de travail, Mars 2011
Mise à jour du Programme de travail, Mars 2011 - Mise à jour du programme de travail, juin 2011
- Liste des textes adoptés, juin 2011
- 2010
- 2009
- 2008
- Modification Work Programme 112008
- Mise à jour programme de travail 112008
- Mise à jour Programme de travail 062008
Mise à jour du programme de travail de la Pharmacopée Européenne (Décisions de la Commission Européenne de Pharmacopée, juin 2008) - Modification Work Programme 062008
Modification of the Work Programme of the European Pharmacopoeia Commission (Decisions of the PhEur Commission, June 2008) - Mise à jour Programme de travail 032008
Mise à jour du programme de travail de la Pharmacopée Européenne (Décisions de la Commission Européenne de Pharmacopée, mars 2008) - Modification Work Programme 032008
Modification of the Work Programme of the European Pharmacopoeia Commission (Decisions of the PhEur Commission, March 2008)
- 2007
- Mise à jour Programme de travail 112007
Mise à jour du programme de travail de la Pharmacopée Européenne (Décisions de la Commission Européenne de Pharmacopée, novembre 2007) - Modification Work Programme 112007
Modification of the Work Programme of the European Pharmacopoeia Commission (Decisions of the PhEur Commission, November 2007) - Modifications Work Programme 062007
Modification of the Work Programme of the European Pharmacopoeia Commission (Decisions of the PhEur Commission, June 2007) - Modifications Work Programme 0307
Modification of the Work Programme of the European Pharmacopoeia Commission (Decisions of the PhEur Commission, March 2007)
- Mise à jour Programme de travail 112007
- 2006
- Modification Work Programme 1106
Modification of the Work Programme of the European Pharmacopoeia Commission (Decisions of the PhEur Commission, November 2006) - Modification Work Programme 0606
Modification of the Work Programme of the European Pharmacopoeia Commission (Decisions of the PhEur Commission, June 2006) - Modification Work Programme 0306
Modification of the Work Programme of the European Pharmacopoeia Commission (Decisions of the PhEur Commission, March 2006)
- Modification Work Programme 1106
- 2005
- Modification Work Programme 1105
Modification of the Work Programme of the European Pharmacopoeia Commission (Decisions of the PhEur Commission, November 2005) - Modification Work Programme 0605
Modification of the Work Programme of the European Pharmacopoeia Commission (Decisions of the European Pharmacopoeia Commission, June 2005) - Modification Work Programme 0305
Modification of the Work Programme of the European Pharmacopoeia Commission (Decisions of the European Pharmacopoeia Commission, March 2005)
- Modification Work Programme 1105
- 2004
- Modification Work Programme 1104
Modification of the Work Programme of the PhEur Commission (Decision of the European Pharmacopoeia Commission, November 2004). - Modification Work Programme 0604
Modification of the Work Programme of the PhEur Commission (Decisions of European Pharmacopoeia Commission, June 2004) - Modification Work Programme 0304
Modification of the Work programme of the PhEur Commission (Decisions of European Pharmacopoeia Commission, March 2004)
- Modification Work Programme 1104
- 2003
- Modification Work Programme 1103
Modification of the Work programme of the PhEur Commission (Decisions of European Pharmacopoeia Commission November 2003)
- Modification Work Programme 0603
Modification of the Work programme of the PhEur Commission (Decisions of European Pharmacopoeia Commission, June 2003).
- Modification Work Programme 1103
- 2011
- Biological Standardisation Programme
- General
- Potentialy genotoxic impurities & PhEur monographs
General Information, Pharmeuropa 20.3, July 2008 - Impuretés potentiellement génotoxiques & monographies
Information générale, Pharmeuropa 20.3, juillet 2008 - Policy Paper: Potentially genotoxic impurities, March 2008
PA/PH/SG (07) 52 COM 1R (English & French) - Procedure 4 Workflow
- Procédure 4 Processus
- Procedure 1 Workflow
- Procédure 1 Processus
- Règles de Déontologie relatives aux Travaux de la Pharmacopée Européenne
PA/PH/Exp. ROP/T (07) 1 DEF (novembre 2010) - Règlement intérieur de la Commission Européenne de Pharmacopée
PA/PH/SG (07) 4 COM DEF (novembre 2010) - Guide relatif aux travaux de la Pharmacopée européenne
PA/PH/SG (10) 42 DEF (novembre 2010) - 1994 Protocol PhEur (English)
- 1994 Protocole PhEur (Français)
- 1964 PhEur Convention (English)
- 1964 Convention Ph Eur (Français)
- Biographical Notes
Biographical Notes - Mrs Marianne Ek & Dr Gerard Lee - Clé des Monographies
- List of Groups of Experts and Working Parties
- Procédure 1 Processus (mis à jour : juillet 2011)
Elaboration/Révision d\'une monographie (mis à jour : juillet 2011) - Procédure 4 Processus (mis à jour : juillet 2011)
Elaboration d\'une monographie (mis à jour : juillet 2011) - Request for revision of monograph or general chapter
- Potentialy genotoxic impurities & PhEur monographs
- Enquiries
- Resolutions
- Lettre circulaire pour Resolution AP-CPH (11) 7
- Resolution AP-CPH (11) 8
4 janvier 2012 - Lettre circulaire pour Resolution AP-CPH (11) 7
- Resolution AP-CPH (11) 7
- Résolution AP-CPH (11) 6 Adoptée par le Comité européen sur les produits et les soins pharmaceutiques (CD-P-PH)
1 Septembre 2011 - Résolution AP-CPH (11) 5 Adoptée par le Comité européen sur les produits et les soins pharmaceutiques (CD-P-PH) (Accord Partiel)
Le 28 mai 2011 - Résolution AP-CPH (11) 5 Adoptée par le Comité européen sur les produits et les soins pharmaceutiques (CD-P-PH)
- Lettre circulaire pour résolutions AP-CPH(11)
- Résolution AP-CPH (12) 1 du Comité européen sur les produits et les soins pharmaceutiques
5 avril 2012 - Résolution AP-CPH (12) 2 du Comité européen sur les produits et les soins pharmaceutiques
5 avril 2012 - Résolution AP-CPH (12) 3 du Comité européen sur les produits et les soins pharmaceutiques
5 avril 2012
- 3R
- BSP004_Somatropin_CRS
- BSP006_D_Vero
- BSP016_HepA_invitro
- BSP019_035_TD_serol
- BSP019_T_serol
- BSP021_IPV_bioassay
- BSP023_IPV_Ag_content
- BSP024_Vet_C_tetani_BRP
- BSP034_P1_Dserol
- BSP034_P1_Ext_Dserol
- BSP034_P2_Dserol
- BSP038_Vet_Erysipelas_serol_BRP
- BSP045_C_tetani_serol_BRP
- BSP055_Newcstle_serol_P1
- BSP055_Newcstle_serol_P2
- BSP076_P_toxin
- BSP079_T_Ig_invitro
- BSP083_aP_ serol
- BSP105_Vet Rabies_serol
- wP_serol_ECVAM
- Pharmacopoeial Discussion Group (PDG)
- GDP Etat des travaux
État des travaux de l\'harmonisation internationale (décembre 2011) - Calendrier prévu janvier 2012
en anglais - GDP Calendrier prévisionnel
Calendrier Prévisionnel pour la publication et la mise en application des textes (Décembre 2011) - PDG Working Procedures
PDG Working Procedures (signed off document Nov. 2007) English only - PDG Statement IH Policy
PDG Statement of International Harmonisation Policy (November 2003) - GDP Énoncé de la politique d\'HI
Énoncé de la politique d\'harmonisation (novembre 2003) - Procédure de travail du GDP
Procédure de travail du Groupe de Discussion des Pharmacopées (GDP) (juin 2010) - GDP Etat des travaux
décembre 2011 - Calendrier prévisionnel décembre 2011
décembre 2011
- GDP Etat des travaux
- European Pharmacopoeia
- Certification EDQM HealthCare European Pharmacopoeia & PDG OMCL Activities & Guidelines Publications, Products Events organised by the EDQM HelpDesk Other Spécifiques
- Procedure of Certification
- CEP - Suspension or withdrawal of a CEP
- PA/PH/CEP (10) 116 Exigences applicable aux notifications déclarées à la DEQM
- CEP - Guidance for electronic applications
- CEP - procedures for CEP applications
- CEP - Guideline on revision/renewal of certificates of suitability to the monographs of the European Pharmacopoeia PA/PH/CEP (04) 2, 4R
- CEP - Procedures for management of revisions/renewals of certificates of suitability to the monographs of the European Pharmacopoeia PA/PH/Exp. CEP/T (04) 18, 2R
- CEP - Nouvelle procédure d’évaluation pour les dossiers frères PA/PH/CEP (09) 141
- CEP Clarification on acceptability of CEP applications
- PA/PH/CEP (08) 60 Clarification on the acceptability of CEP applications for sterile grade material
欧洲药典适应性证书 : 无菌级CEP证书申请受理说明 (English/Chinese) - CEP Note for the applicants: procedure for validation of new applications
- PA/PH/Exp. CEP/T (08) 37 Note for the applicants: Procedure for validation of new applications
申请人须知：新CEP申请验收程序 (English/Chinese) - PA/PH/Exp. CEP/T (08) 37 Note aux demandeurs : Procédure de validation des nouvelles demandes
- Explanatory Note on the Revised Version of the Resolution AP-CSP (07)1 (Chinese)
- PA/PH/CEP (04) 2 3R: Guideline on Requirements for Revisions/Renewals of Certificates
- CEP Procedure Revised Version
- AP-CSP (07) 1: Certification Procedure Revised Version (Chinese)
- PA/PH/CEP (04) 2, 3R Guide relatif aux exigences applicables en matière de révision/renouvellement des certificats de conformité aux monographies de la Pharmacopée européenne
- PA/PH/CEP(04) 2, 3R Guideline on Requirements for Revision/Renewal of Certificates, May 2008
注意：该文件最近进行了修订（详情见英文文本）。中文文本将尽快发布。 - CEP - Procedure for Management of Revisions and Renewals
- PA/PH/Exp. CEP/T (04) 18, 1R Procédures de traitement des demandes de révision/renouvellement de certificats de conformité aux monographies de la Pnarmacopée européenne
- PA/PH/Exp. CEP/T (04)18 1R New Procedures for management of revisions/renewals of certificates, June 2008
注意：该文件最近进行了修订（详情见英文文本）。中文文本将尽快发布。(English/Chinese) - PAPHExpCEPT0426: Revision of TSE Certificates for the 5th Edition of the European Pharmacopoeia (15/11/04)
- Renewal of Certificates of Suitability - Implementation of the Amendments to the Directives 2001/83/EC and 2001/82/EC (Revised 03/01/06)
- Policy on stating manufacturing sites on CEPs
- PA/PH/CEP (10) 85 Plus de changement accepté durant l’évaluation
- CEP - La position de la DEQM concernant les demandes de CEP pour les substances biologiques PA/PH/CEP (09) 152 rev 01
- PA/PH/CEP (10) 118 1R (FR)
PA/PH/CEP (10) 118 1R (FR) - PA/PH/CEP (11) 43 Rapport du programme pilote international d’inspection des substances actives à usage pharmaceutique
Rapport du programme pilote international d’inspection des substances actives à usage pharmaceutique - PA/PH/CEP (11) 47 Clarification concernant l’évaluation des données de stabilité dans le cadre de la procédure de Certification
PA/PH/CEP (11) 47 - PA/PH/CEP (11) 48 Evaluation du conditionnement dans le cadre de la procédure de Certification
PA/PH/CEP (11) 48
- Application Forms and QOS Template
- CEP Request for Technical Advice
- CEP_Template for Quality Overall Summary
- New Application
- Application Revision Renewal
- Formulaire de dépôt pour les nouvelles demandes (août 2011)
Formulaire de dépôt pour les nouvelles demandes (août 2011, en anglais) - CEP - Formulaire de dépôt pour les révisions et renouvellements
- Content of Dossier
- Chemical purity & microbiological quality
- CEP - Top Ten Deficiencies New Applications
October to December 2009 - CEP - Content of the Dossier for Chemical Purity & Microbiological Quality
- Content of the Dossier for chemical purity and microbiological quality
PA/PH/CEP 04 1 4R: 欧洲药典适用性证书: 化学合成和有微生物品质要求品种的文件内容
- CEP - Top Ten Deficiencies New Applications
- Herbals products
- Sterile active substances
- Substance for TSE risk assessment
- Chemical purity & microbiological quality
- List of assessors
- Certification Liste des assesseurs (mise à jour le 01/02/2012)
mise à jour le 01/02/2012
- Certification Liste des assesseurs (mise à jour le 01/02/2012)
- General
- CEP Terms of Reference for Certif
- Implementation of the European Pharmacopoeia supplement 6.3
- Implementation of the European Pharmacopoeia supplement 6.4
- Implementation of the European Pharmacopoeia supplement 6.5
- PA/PH/CEP (10) 86 Changement de contacts
- CEP - update of monographs
- PA/PH/CEP (10) 118
- PA/PH/CEP (11) 18 FR
- CEP - Refus d’informations provenant de tierces parties
- CEP - Update of monographs for impurities
- CEP Mise à jour de monographies concernant la limite pour les impuretés non spécifiées
- PA/PH/CEP (11) 29
PA/PH/CEP (11) 29 - Circular Letter, TSE 2011
- Note to the attention of all holders of TSE certificates of suitability:
- Communication with EDQM Certification Division
- CEP-Programme de rationalisation des inspections BPF-PAPHCEP1230FR
- CEP Cas de falsification de données dans le cadre de la procédure CEP
- Important notice to CEP holders template letter
- Notice for CEP holders
- Monthly Report of Activities
- 2012
- 2011
- Certification rapport mensuel avril 2011 PA/PH/CEP (11)31
- Certification rapport mensuel mars 2011 PA/PH/CEP (11)26
- Certification rapport mensuel février 2011 PA/PH/CEP (11)16
- Certification rapport mensuel janvier 2011 PA/PH/CEP (11)12
- Certification rapport mensuel mai 2011 PA/PH/CEP (11)37
- Certification rapport mensuel juin 2011 PA/PH/CEP (11)45
- Certification rapport mensuel juillet 2011 PA/PH/CEP (11) 57
Juillet 2011 - Certification rapport mensuel août 2011 PA/PH/CEP (11) 62
- Certification rapport mensuel septembre 2011 PA/PH/CEP (11) 71
- CEP monthly report October 2011
- CEP monthly report November 2011
- Registration fees
- Inspections
- Rapport du programme pilote international d’inspection des substances actives à usage pharmaceutique
Rapport du programme pilote international d’inspection des substances actives à usage pharmaceutique
- Rapport du programme pilote international d’inspection des substances actives à usage pharmaceutique
- Technical advice
- Samples
- Procedure of Certification
- OMCL Activities & Guidelines EDQM HealthCare European Pharmacopoeia & PDG Certification Publications, Products Events organised by the EDQM HelpDesk Other Spécifiques
- General European OMCL Network Activities
- General procedure for Sampling and Testing of Centrally-Authorised Products (PA/PH/CAP (05) 49 6R)
Adopted 13/12/2010 - Letter EDQM and HMA
HMA Working Group on Product Testing Document - Principles for Mutual Recognition of Control results
HMA Working Group on Product Testing Document (Version 1.0) - MRP/DCP Post-Marketing surveillance
Co-operation in post-marketing surveillance of Mutual Recognition /Decentralised Procedure Products (PA/PH/OMCL 06 116 9R, February 2011) - PA/PH/OMCL (07) 79 18Rcorr Terms of Reference
Terms of Reference for the General European OMCL Network (GEON) of the Council of Europe (PA/PH/OMCL (07) 79 18Rcorr) - PA/PH/OMCL (07) 89 8R - Annex 1 to the GEON Terms of Reference: Definition of an OMCL and OMCL Status within the GEON
- PA/PH/OMCL (07) 90 4R - Annex 2 to the GEON Terms of Reference: Factors for determining OMCL status within the GEON
- PA/PH/OMCL (09) 45 7R - Annex 3 List of GEON members
- NEW: PA/PH/OMCL (08) 04 12R - Annex 4 to the GEON Terms of Reference: Questionnaire to query the OMCL status of present and future members of the GEON
- PA/PH/OMCL (09) 87 3R OMCL Network support for the implementation of the CoE MEDICRIME Convention
- Survey extraneous agents
- General procedure for Sampling and Testing of Centrally-Authorised Products (PA/PH/CAP (05) 49 6R)
- Human Biologicals (OCABR)
- Guidelines
- Administrative procedures
- Procedure For Official Control Authority Batch Release of Centrally Authorised Immunological Medicinal Products For Human Use And Medicinal Products Derived From Human Blood And Plasma (2011)
December 2011 - REVISED: EU Administrative Procedure for Official Control Authority Batch Release 2011
December 2011 - Annex_III 28/03/12
- Procedure For Official Control Authority Batch Release of Centrally Authorised Immunological Medicinal Products For Human Use And Medicinal Products Derived From Human Blood And Plasma (2011)
- Guidelines for blood products
- REVISED: Clotting Factor Concentrates, Plasma Inhibitor Concentrates and Fibrin Sealants
December 2011 - REVISED: Human albumin
December 2011 - REVISED: Human immunoglobulin
December 2011 - REVISED: Human Plasma (pooled & treated for virus inactivation) formerly Solvent-Detergent (SD) Plasma
December 2011 - Official Control Authority Protocol for Approval of Plasma pools
December 2011
- REVISED: Clotting Factor Concentrates, Plasma Inhibitor Concentrates and Fibrin Sealants
- Guidelines for vaccines
- REVISED: BCG Vaccine
December 2011 - Cell Cultured Influenza Vaccine (Surface Antigen, Inactivated) NEW GUIDELINE
December 2011 - REVISED: Cholera vaccine (Oral, Inactivated)
December 2011 - REVISED: Diphtheria and Tetanus vaccine (Absorbed)
December 2011 - REVISED: Diphtheria, Tetanus and Hepatitis B (rDNA) Combined vaccine (Adsorbed)
December 2011 - REVISED: Diphtheria, Tetanus and Pertussis (Acellular component) Combined Vaccine (adsorbed)
December 2011 - REVISED: Diphtheria, Tetanus and Pertussis (Whole cell) Combined vaccine (Adsorbed)
December 2011 - REVISED: Diphtheria, Tetanus and Poliomyelitis (Inactivated) Combined Vaccine (Adsorbed)
December 2011 - REVISED: Diphtheria, Tetanus, Pertussis (Acellular component) and Haemophilus Type B Conjugate Combined vaccine (Adsorbed)
December 2011 - REVISED: Diphtheria, Tetanus, Pertussis (Acellular component) and Hepatitis B (rDNA) Combined vaccine (Adsorbed)
December 2011 - REVISED: Diphtheria, Tetanus, Pertussis (Acellular component), Poliomyelitis (Inactivated) and Haemophilus Type B Conjugate Combined vaccine (Adsorbed)
December 2011 - REVISED: Diphtheria, Tetanus, Pertussis (Acellular component), Poliomyelitis (Inactivated) Combined vaccine (Adsorbed)
December 2011 - REVISED: Diphtheria, Tetanus, Pertussis (Acellular Component), Poliomyelitis (Inactivated), Hepatitis B (rDNA) and Haemophilus Type B Conjugate Combined Vaccine (Absorbed)
December 2011 - REVISED: Diphtheria, Tetanus, Pertussis (Acellular component), Poliomyelitis (Inactivated), Hepatitis B (rDNA) with separate Haemophilus Type B Conjugate Combined vaccine (Absorbed)
December 2011 - REVISED: Diphtheria, Tetanus, Pertussis (Whole cell) and Poliomyelitis (Inactivated) Combined vaccine (adsorbed)
December 2011 - REVISED: Diphtheria, Tetanus, Pertussis (Whole cell), Poliomyelitis (Inactivated) and Haemophilus Type B Conjugate Combined vaccine (Adsorbed)
December 2011 - REVISED: Haemophilus Type B Conjugate and Hepatitis B (rDNA) Combined Vaccine
December 2011 - NEW: Haemophilus Type B Conjugate and Meningococcal C Conjugate Combined Vaccine
Haemophilus Type B Conjugate and Meningococcal C Conjugate Combined Vaccine (2011) - REVISED: Haemophilus Type B Conjugate Vaccine
December 2011 - REVISED: Hepatitis A (Inactivated) and Hepatitis B (rDNA) Combined Vaccine (Absorbed)
December 2011 - REVISED: Hepatitis A (Inactivated) and Typhoid Polysaccharide Combined Vaccine (Adsorbed)
December 2011 - REVISED: Hepatitis A (Inactivated) and Typhoid Polysaccharide Combined Vaccine (Absorbed) for Mix-At-Use Format Products
December 2011 - REVISED: Hepatitis A Vaccine (Inactivated, Absorbed)
December 2011 - REVISED: Hepatitis A (Virosomal) Vaccine
December 2011 - REVISED: Hepatitis B (rDNA) Vaccine
December 2011 - REVISED: Human Papillomavirus (rDNA) Vaccine
December 2011 - REVISED: Influenza Vaccine
December 2011 - Influenza Vaccine (Surface Antigen, Inactivated, Virosome)
December 2011 - REVISED: Japanese Encephalitis (JE) Vaccine, Inactivated
December 2011 - REVISED: Live Attenuated Influenza Vaccine produced on eggs
December 2011 - REVISED: Measles, Mumps, and/or Rubella Component Combined Vaccine
December 2011 - REVISED: Measles, Mumps, Rubella & Varicella Combined vaccine
December 2011 - REVISED: Measles Vaccine
December 2011 - REVISED: Meningococcal Polysaccharide Vaccine
- REVISED: Monovalent or multivalent meningococcal polysaccharide conjugate vaccine
2011 - REVISED: Multivalent Pneumococcal Polysaccharide Conjugate Vaccine
December 2011 - REVISED: Mumps Vaccine
December 2011 - Pandemic Influenza vaccine REVISED
Pandemic Influenza Vaccine (2009) - REVISED: Pertussis Vaccine (Acellular Component, adsorbed)
May 2012 - REVISED: Pneumococcal Polysaccharide Vaccine
December 2011 - REVISED:Poliomyelitis Vaccine (Inactivated)
December 2011 - REVISED: Poliomyelitis Vaccine (Oral) (OPV) - Monovalent Bulk
December 2011 - REVISED: Poliomyelitis Vaccine (Oral) (OPV) - Trivalent Vaccine
December 2011 - REVISED: Rabies vaccine
December 2011 - REVISED: Rotavirus Vaccine
December 2011 - REVISED: Rubella Vaccine
December 2011 - REVISED: Tick-Borne Encephalitis (TBE) Vaccine
December 2011 - REVISED: Typhoid Polysaccharide Vaccine
December 2011 - REVISED: Typhoid Vaccine (Live-Strain type 21a Oral)
December 2011 - REVISED: Vaccine containing Vaccinia virus produced in cell culture (Smallpox vaccine)
December 2011 - REVISED: Varicella Vaccine & Shingles Vaccine
December 2011 - REVISED: Yellow Fever Vaccine
May 2012
- REVISED: BCG Vaccine
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mise à jour le 22/05/2012
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- UPDATED: Purified protein derivative (PPD), bovine
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- UPDATED: Swine Erysipelas Vaccine (inactivated)
- UPDATED: Swine Erysipelas Vaccine (live)
- UPDATED: Tuberculin purified protein derivative (PPD), avian
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PA/PA OMCL (05) 48 DEF CORR (December 2007) - Validation of Analytical Procedures
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PA/PA/OMCL (05) 49 DEF CORR (December 2007) - Uncertainty of Measurements - Part II (Other than compliance testing)
PA/PH/OMCL (07) 106 DEF (December 2007) - Standard Aide-Mémoire for the Mutual Joint Audit of OMCLs
PA/PH/OMCL (06) 72 2R (FORM/158-Rev.02) (February 2011) - Aide-Memoire for environmental conditions & treatment of biological models
PA/PH/OMCL (07) 75 2R (Form/159-Rev. 2) (January 2011) - Evaluation & Reporting of Results
PA/PH/OMCL (07) 28 DEF CORR (December 2007) - UPDATED: Qualification of Equipment (core document)
PA/PH/OMCL (08) 73 2R (July 2011) - UPDATED: Annex 1: Qualification of HPLC Equipment
PA/PH/OMCL (11) 04 (July 2011) - Annex 2: Qualification of GC equipment
PA/PH/OMCL (06) 86 DEF (October 2006) - Annex 3: Qualification of UV-Visible spectrophotometers
PA/PH/OMCL (07) 11 DEF CORR (December 2007) - Annex 4: Qualification of IR spectrophotometers
PA/PH/OMCL (07) 12 DEF CORR (December 2007) - UPDATED: Annex 5 Qualification of Automatic Titrators
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PA/PH/OMCL (10) 86 2R (July 2011) - Validation of Computerised Systems - Core Document
PA/PH/OMCL (08) 69 3R (July 2009) - Annex 1: Validation of computerised calculation systems: example of validation of in-house software
PA/PH/OMCL (08) 87 2R Validation of Computerised Systems (July 2009) - Annex 2: Validation of Databases (DB), Laboratory Information Management Systems (LIMS) and Electronic Laboratory Notebooks (ELN)
PA/PH/OMCL (08) 88 R Validation of Computerised Systems (July 2009) - Annex 3: Validation of computers as part of test equipment
PA/PH/OMCL (08) 89 R Validation of Computerised Systems (July 2009) - Archiving within the OMCL Network
PA/PH/OMCL (07) 105 DEF (April 2001) - Management of Reagents
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- AP-CDP (10) 1 Suppression de la monographie, 15 mars 2010
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- AP-CPH (10) 2 Supplement 7.1 Mise en application
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- 6th Edition initial volumes 6.0
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- Lettre Circulaire Résolution AP-CPH (09) 4 (French)
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- 6th Edition Implementation Dates: AP-CSP (06) 04
- AP-CPH (07) 3 Supplement 6.1 Date of implementation
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- AP-CPH (07) 4 Supplement 6.2 Date of implementation
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- AP-CPH (07) 5 Supplement 6.3 Mise en application
- AP-CPH (07) 5 Supplement 6.3 Date of implementation
- AP-CPH (08) 1 Supplement 6.4 Date of implementation
- AP-CPH (08) 1 Supplement 6.4 Mise en application
- AP-CPH (08) 2 Supplement 6.5 Date of implementation
- AP-CPH (08) 2 Supplement 6.5 Mise en application
- AP-CPH (08) 3 Supplement 6.6 Date of implementation
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- AP-CPH (08) 5 European Committee on Pharmaceuticals & Pharmaceutical Care
Adopted by the European Committee on Pharmaceuticals and Pharmaceutical Care (CD-P-PH) (Partial Agreement) on 18 July 2008 - AP-CPH (08) 5 Comité européen sur les produits et les soins pharmaceutiques
Adoptée par le Comité européen sur les produits et les soins pharmaceutiques (CD-P-PH) (Accord Partiel) le 18 juillet 2008 - AP-CPH (09) 1 Supplement 6.7 Date of implementation
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- 5th Edition Supplement 5.8
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English Cumulative Index 5th Edition 5.8 - F Index 5th 5.8
French Cumulative Index 5th Edition 5.8
- E Comments Supplement 5.8
- 5th Edition Supplement 5.7
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Comments concerning some revised/corrected texts published in Supplement 5.7 - E Index 5th 5.7
English Cumulative Index 5th Edition 5.7 - F Index 5th 5.7
French Cumulative Index 5th Edition 5.7 - E Contents List 5.7
English List of Contents Supplement 5.7 - F Contents List 5.7
French List of Contents Supplement 5.7
- E Comments Supplement 5.7
- 5th Edition Supplement 5.6
- E Comments Supplement 5.6
Comments concerning some revised/corrected texts published in Supplement 5.6 - E Index 5th 5.6
English Cumulative Index 5th Edition 5.6 - F Index 5th 5.6
French Cumulative Index 5th Edition 5.6 - E Contents List 5.6
English List of Contents Supplement 5.6 - F Contents List 5.6
French List of Contents Supplement 5.6
- E Comments Supplement 5.6
- 5th Edition Supplement 5.5
- E Comments Supplement 5.5
Comments concerning some revised/corrected texts published in Supplement 5.5 - E Index 5th 5.5
English Cumulative Index 5th Edition 5.5 - F Index 5th 5.5
French Cumulative Index 5th Edition 5.5 - E Contents List 5.5
English List of Contents Supplement 5.5 - F Contents List 5.5
French List of Contents Supplement 5.5
- E Comments Supplement 5.5
- 5th Edition Supplement 5.4
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Comments concerning some revised/corrected texts published in Supplement 5.4 - E List New Reagents
List of new reagents: Supplement 5.4 - F Index 5th 5.4
French Cumulative Index 5th Edition 5.4 - E Index 5th 5.4
English Cumulative Index 5th Edition 5.4 - E Contents List 5.4
English List of Contents Supplement 5.4 - F Contents List 5.4
French List of Contents Supplement 5.4
- E Comments Supplement 5.4
- 5th Edition Supplement 5.3
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Comments concerning some revised/corrected texts published in Supplement 5.3 - E Index 5th 5.3
English Cumulative Index 5th Edition 5.3 - F Index 5th 5.3
French Cumulative 5th Edition 5.3 - E Contents List 5.3
English List of Contents Supplement 5.3 - F Contents List 5.3
French List of Contents Supplement 5.3
- E Comments Supplement 5.3
- 5th Edition Supplement 5.2
- E Comments Supplement 5.2
Comments concerning some revised/corrected texts published in Supplement 5.2 - E Index 5th 5.2
English Cumulative Index 5th Edition 5.2 - F Index 5th 5.2
French Cumulative Index 5th Edition 5.2 - E Contents List 5.2
English List of Contents Supplement 5.2 - F Contents List 5.2
French List of Contents Supplement 5.2
- E Comments Supplement 5.2
- 5th Edition Supplement 5.1
- E Comments Supplement 5.1
Comments concerning some revised/corrected texts published in Supplement 5.1 - E Contents list 5.1
English List of Contents Supplement 5.1 - F Contents List 5.1
French List of Contents Supplement 5.1
- E Comments Supplement 5.1
- 5th Edition initial volumes 5.0
- E Comments 5th Edition
Comments concerning some revised/corrected texts published in the 5th Edition - E Contents List 5th
English List of Contents 5th Edition - F Contents List 5th
French List of Contents 5th Edition
- E Comments 5th Edition
- 5th Edition implementation dates and texts deleted
- APCSP0603E
Supplement 5.8 date of implementation = AP-CSP (06) 3 - APCSP0602E
Supplement 5.7 date of implementation = AP-CSP (06) 2 - APCSP0601E
Suppression Method of Analysis (2.9.13) = AP/CSP (06) 1 - APCSP0504E
Suppression Monograph Glucagon (0612) = AP/CSP (05) 4 - APCSP0503E
Supplement 5.6 date of implementation = AP-CSP (05) 3 - APCSP0502E
Supplement 5.5 date of implementation = AP-CSP (05) 2 - APCSP0501E
Supplement 5.4 date of implementation = AP-CSP (05) 1 - APCSP0404E
List of monographs deleted = AP/CSP (04) 4 - APCSP0403E
Supplement 5.3 date of implementation = AP/CSP (04) 03 - APCSP0402E
Supplement 5.2 date of implementation = AP/CSP (04) 2 - APCSP0401E
Supplement 5.1 date of implementation = AP/CSP (04) 1 - APCSP0304E
List of monographs deleted = AP/CSP (03)4
- APCSP0303E
5th Edition date of implementation = AP/CSP (03)03
- APCSP0603E
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English comments concerning some revised texts Supplement 4.8 - E comments revised texts Suppl 4.7
English comments concerning some revised texts Supplement 4.7 - List revised texts 4th Edition 4.0
Revised texts published in the 4th Edition - E comments revised texts Suppl 4.6
English comments concerning some revised texts Supplement 4.6 - E comments revised texts Suppl 4.5
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List of monographs deleted = AP/CSP (02)6 - APCSP0204E
List of monographs deleted = AP/CSP (02)4 - APCSP0203E
Supplement 4.5 date of implementation = AP/CSP (02)03 - APCSP0201
Supplement 4.4 date of implementation = AP/CSP (02)01 - APCSP022E
List of monographs deleted = AP/CSP (02)2 - APCSP017E
Supplement 4.3 date of implementation = AP/CSP (01)07 - APCSP016E
List of monographs deleted = AP/CSP (01)6 - APCSP 015E
Supplement 4.2 date of implementation = AP/CSP (01)5 - APCSP 014E
List of monographs deleted = Res AP/CSP (01)4 - APCSP013E
Supplement 4.1 date of implementation = Res AP/CSP (01)3 - APCSP012E
List of monographs deleted = Res AP/CSP (01)2 - APCSP011E
4th Edition initial volume date of Implementation = Res AP/CSP (01)1
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- 4th Edition: Comments concerning revised texts
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- Posters
- Symposium on Implementation of Pathogen Reduction Technologies For Blood Components, Strasbourg, France, 2-3 September 2010
- International Conference on counterfeit medical products, 15-16 April 2010, Basel, Switzerland
- EDQM Symposium, South Africa, 12-13 April 2010
- Training Session on the Guide for the elaboration and use of monographs on IVMPs, 18-19 March 2010
- Joint Symposium IPA-EDQM-IPC, 28-29 January 2010, Mumbai, India
- Expert Workshop Pharmaceutical Care, 10 December 2010
- 2009
- CombiStats Training, 19-20 November 2009
- Expert Workshop: 19 November 2009
- Proceedings
- Proceedings Expert Workshop 19 November 2009
Assessing the quality of patient-centred pharmaceutical care in Europe
- Proceedings Expert Workshop 19 November 2009
- Proceedings
- SAFYBI, Buenos Aires, Argentina, 27-29 October 2009
- Batch release for human vaccines, 15-16 October 2009
- 2009 Organ Donation Congress, 4-7 October 2009
- 2009 European Organ Donation Day Congress Programme
4-7 October Berlin (Germany)
- 2009 European Organ Donation Day Congress Programme
- Herbal drugs and herbal drug preparations, 25 September 2009
- List of participants
- Programme
- Proceedings
- Presentations
- PharmSciFair, Nice, France, 8-12 June 2009
- EDQM symposium - Final Programme, 9 June 2009
Sourcing of Active Pharmaceutical Ingredients (APIs)
- EDQM symposium - Final Programme, 9 June 2009
- API from Bioprocesses, APIB 2009, 3-6 June 2009
- Optimal Clinical Use of Blood Components, Wildbad Kreuth, Germany, 24-25 April 2009
- Expofarma Interphex, Mexico City, Mexico, 22-24 April 2009
- ISBT Regional Congress, Cairo, Egypt, 21-25 March 2009
- Expert Workshop, 24th September 2009
- Proceedings
- Proceedings Expert Workshop, 24th September 2009
Promoting standards for the quality and safety assurance of pharmacy-prepared medicinal products
- Proceedings Expert Workshop, 24th September 2009
- Proceedings
- 2008
- Regulatory submission procedures in EU, 13-14 November
- European Organ Donation and Transplantation Day, 18 October
- Presentations
- The Results and Possibilities Of Modern Treatment With Transplantation - Ferdinand Mülhbacher
- Equitable Access to Transplantation - Axel Rahmel
- Eurocet - Dr Alessandro Nanni Cota
- Heart Transplantation, Stem Cell Therapy and Mechanical Circulatory Support
- Global Overview on Donation - Beatriz Domiguez-Gil
- Personal Reflection and Public Debate on Organ Donation: A Teaching aid from the Council of Europe - Tina Garani-Papadatos
- Ethical Questions related to Donation - Guenter Kirste
- Council of Europe Actions and Activities in Organ Donation - Per Pfeffer
- Project: The Celebration of 10th European Donation Day
- Programme
- Presentations
- Pharmaceutical Reference Standards, 9-10 October
- List of Participants
- Programme
- Proceedings
- Presentations
- Posters
- Workshop on the Characterisation of Heparin Products, 19-20 June
- Summary of Workshop Sessions
- List of Participants
- Speakers\' Biographical Notes
- Programme
- Presentations
- Session 1: Contamination of heparin - Part 1
Data from the field - market surveillance - batch results
Reaction from the licencing authorities - Session 1: Contamination of heparin - Part 2
Possible solutions for the future - view points from industry and academia - Session 1: Contamination of heparin - Part 3
Pharmacopoeias - plans for revision - Session 2: Global harmonisation - Part 1
Characterisation of UFH samples from the past decade
Physio-chemical characterisation - Session 2: Global harmonisation - Part 2
Characterisation of UFH samples from the past decade
Physico-chemical characterisation - Session 2: Global harmonisation - Part 3
Harmonisation of methods for estimation of potency - Session 3: Low molecular weight heparin
Unfractionated heparin as starting material for LMW heparins
Characterisation of LMW heparins
- Session 1: Contamination of heparin - Part 1
- Alternatives to animal testing, 23-24 April
- List of Participants
- Programme
- Proceedings
- Presentations
- Session 1: Current regulations & review of progress
Session 1: Current regulations on alternatives and review of progress, 23 April - Session 2: Human Vaccines
Session 2: Human Vaccines - Safety and Potency, 23 April - Session 3: Veterinary Vaccines
Session 3: Veterinary Vaccines, 23 April - Session 4: Biotherapeutics
Session 4: Biotherapeutics, 24 April - Session 5: New Technologies
Session 5: New Technologies, 24 April - Session 6: Case Studies & Validation studies
Session 6: Case studies and validation studies, 24 April - Drawbacks of 3Rs implementation
Preliminary Feedback from an EDQM survey: an overview of the effective transposition of the 3Rs progress implemented in the Ph. Eur. monographs, and to identify and address causes for non-transposition or non-use in control activities
- Session 1: Current regulations & review of progress
- Posters
- 2007
- Working across disciplines and borders, 6-7 December
- Programme
- Background Documents
- 2007 Survey
2007 Survey on training needs and competencies of member states as regards combating counterfeit medicines and other forms of pharmaceutical crimes - Introduction
- 2007 Survey
- CPhI Worldwide 2007, Milan, 2-4 October
- European Co-operation and Synergy in Quality Stadards, 15-16 June
- Programme
- List of Participants
List of participants, Symposium, 15-16 June 2007 - Prog Final 15-16
Final Programme - European co-operation & synergy in quality standards beyond the European Pharmacopoeia, 15-16 June 2007, Strasbourg, France
- List of Participants
- Proceedings
- Presentations
- Session 1: General Introduction
Session 1: General Introduction, 15 June 2007 - Session 2: Licensing
Session 2: Licensing, 15 June 2007 - Session 3: National Experiences of Formularies
Session 3: National Experiences of Formularies, 16 June 2007 - Session 4: Radiopharmaceuticals
Session 4: The specific case of radiopharmaceuticals manufactured extemporaneously in hospital radiopharmacies, 16 June 2007
- Session 1: General Introduction
- Posters
- Symposium Poster Session
Poster Session, 15-16 June 2007
- Symposium Poster Session
- Programme
- New Frontiers in the Quality of Medicines, 13-15 June
- Programme
- Final Prog New Frontiers
Final Programme - New Frontiers in the Quality of Medicines, 13-15 June 2007, Strasbourg, France - List of Participants Conference
List of participants, Conference, 13-15 June 2007 - Workshops & One-to-One Revised
Final Workshop & One-to-One Programme, 14 June 2006 - REVISED
- Final Prog New Frontiers
- Proceedings
- Presentations
- Plenary Sessions 13th & 15th June
- Plenary Session 13 June - Part 2
Plenary Session - Perspectives for co-operation: Partnership with the Regulatory Authorities & the PDG Pharmacopoeias, 13th June 2007 (Part 2) - Plenary Session 13 June - Part 1
Plenary Session - International Co-operation & Synergy in Quality Standards: Vision from Europe, 13th June 2007 (Part 1) - Plenary Session 13 June - Part 3
Plenary Session - Perspectives for co-operation: Partnership with Industry, 13th June 2007 (Part 3) - Plenary Session 15 June Part 2
Plenary Session - Action plan for the future: Recommendations from the Industry, 15th June 2007 (Part 2) - Plenary Session 15 June Part 1
Plenary Session - Action plan for the future: Recommendations from the Industry, 15th June 2007 (Part 1) - Russian Health and Pharmaceutical Authorities, The Russian Federation
Mr Nicolay Yurgel, Ministry of Healthcare and Social Development, 13th June 2007
- Plenary Session 13 June - Part 2
- Workshop Sessions 14th June
- Building a partnership for investigation of counterfeit medicines
Workshop - Building a partnership for the investigation of counterfeit medicines - Certification: How to use a CEP
Workshop - Certification: How to use a Certificate - Certification: Inspections
Workshop - Certification: Inspections - European Biological Standardisation Programme
Workshop - European Biological Standardisation Programmme - Excipients: FRC & ICH Q8
Workshop - Excipients: Functionality related tests (FRC) & ICH Q8 - Herbals: Implementation of the new legislative framework
Workshop - Herbals: Implementation of the new legislative framework - Herbals: Traditional Chinese medicines
Workshop - Herbals: Traditional Chinese Medicines - Homoeopathy
Workshop - Homoeopathy - International harmonisation: Microbiological techniques
Workshop - International harmonisation: Microbiological techniques - New challenges for Pharmacopoeias
Workshop - New challenges for Pharmacopoeias - Partnership developed within the OMCLs
Workshop - Partnership developed within the Official Medicines Control Laboratories (OMCLs) - PDG and the ICH Q4B
Workshop - Pharmacopoeial Discussion Group & the ICH Q4B - Quality standards for biologicals
Workshop - Quality standards for biologicals - Reference standards
Workshop - Reference Standards: How to characterise them, key elements and qualification - Updating monographs & methods (Part 1)
Workshop - Updating monographs and methods (Part 1) - Updating monographs and methods (Part 2)
Workshop - Updating monographs & methods (Part 2) - Workshop Conclusions
Workshop Conclusions
- Building a partnership for investigation of counterfeit medicines
- Plenary Sessions 13th & 15th June
- Posters
- Conf Poster Session
Poster Session, 13-15 June 2007
- Conf Poster Session
- Programme
- China Symposium, 23-24 May
- Final Prog China, 23-24 May 2007
The European Pharmacopoeia 6th Edition - Shanghai, 23-24 May 2007
- Final Prog China, 23-24 May 2007
- India Symposium, 4-5 May
- Programme Hyderabad 4-5 May 2007
Regulatory Submission Procedures in EU – APIs & Drug Products, Hyderabad, 4-5 May 2007
- Programme Hyderabad 4-5 May 2007
- Working across disciplines and borders, 6-7 December
- 2006
- 2006 Conference Archive
2006 Conference Proceedings & Presentations - Europe against counterfeit medicines, Moscow, 23-24 October
- Programme
- Speeches & Presentations
- Day 1, 23 October
- Day 2, 24 October
(Some speeches are only available in French) - Introduction
- Declaration
- ETIF, 24-27 October 2006, Buenos Aires, Argent
- Avian Influenza Vaccines Symposium, Strasbourg, 19-20 October
- Programme
- Final Prog Avian Flu
Final Programme Avian Influenza Symposium, Strasbourg, 19-20 October
- Final Prog Avian Flu
- Proceedings
- Proceedings Avian Flu Vaccines
Proceedings of the symposium on Avian Influenza Vaccines
- Proceedings Avian Flu Vaccines
- Programme
- New Microbiology Chapters, Strasbourg, 2-3 October
- Programme
- Final Programme
Final Programme Microbiology Chapters Symposium, Strasbourg, 2-3 October - List Participants Microbiology
List of participants, Microbiology Symposium, 2-3 October 2006
- Final Programme
- Proceedings
- Proceedings Microbiology Chapters
Proceedings of the symposium on New Microbiology Chapters
- Proceedings Microbiology Chapters
- Presentations
- Opening Session
Opening Session: New microbiology chapters - Session I: Part 1 Slides
Session I: Microbiological contamination of non-sterile products (Part 1) - Session I: Part 2 Slides
Session I: Microbiological contamination non-sterile products (Part 2) - Session II: Part 1 Slides
Session II: Alternative methods for control of microbiological quality (Part 1) - Session II: Part 2 Slides
Session II: Alternative methods for control of microbiological quality (Part 2) - Session II: Part 3 Slides
Session II: Alternative methods for control of microbiological quality (Part 3)
- Opening Session
- Programme
- Impurities control: setting specifications for antibiotics and peptides, 21-22 September
- Programme
- Impurities Final programme
Impurities Control: setting specifications for antibiotics and peptides - List Participants Impurities
List of participants, Impurities Control Symposium, 21-22 September 2006
- Impurities Final programme
- Proceedings
- Proceedings Impurities Control
Proceedings of the symposium on Impurities Control: Setting specifications for antibiotics and peptides
- Proceedings Impurities Control
- Presentations
- Antibiotics Presentations
Impurities control: setting specifications for Antibiotics (21 September 2006) - Antibiotics Workshops
Issues discussed and the conclusions reached during the Antibiotics workshops (21 September 2006) - Peptides Presentations
Impurities control: setting specifications for Peptides (22 September 2006)
- Antibiotics Presentations
- Programme
- CPhI China 2006, Shanghai, China
- Programme
- Prog CPhI Sympo
Programme European Pharmacopoeia Symposium, 27 June, 14h00-16h00, Hall W2, Meeting Room M9
- Prog CPhI Sympo
- Presentations
- An overview of EDQM publications & online services - Mrs C. Larsen Le Tarnec
An overview of EDQM publications and online services - The Certification of Suitability to the PhEur monograph (CEP) - Dr C. Pouget
The Certification of Suitability to the PhEur monograph (CEP) - The PhEur: General concepts & specific monographs - a detailed analysis - Dr C.Coune
- An overview of EDQM publications & online services - Mrs C. Larsen Le Tarnec
- Programme
- IDMA
- Programme
- IDMA Final Prog
IDMA & EDQM Symposium, Mumbai, India, 23-24 January 2006
- IDMA Final Prog
- Programme
- 2006 Conference Archive
- 2005
- 2005 Proceedings Archive
2005 Conference Proceedings - IPC Congress, Hyderabad, India, 2-4 December
- Programme
- IPC Programme
Programme - IPC Congress, Hyderabad, India, 3 December 2005
- IPC Programme
- Programme
- Certification Conference, Istanbul, 27-28 October
- Programme
- Final Programme
Programme: International Conference on Certification, 27-28 October 2005
- Final Programme
- Presentations
- Plenary Session
- Plenary Presentations
Plenary Sessions Presentations, 27 & 28 October 2005
- Plenary Presentations
- Workshop: Revision & renewal procedures
- Rev Ren Presentations
Workshop 1: New procedures for the revision and renewal of certificates
- Rev Ren Presentations
- Workshop: Deficiencies in dossiers
- Deficiencies Presentations
Workshop 2: An outline of the main deficiencies in dossiers and how to avoid them
- Deficiencies Presentations
- Workshop: Sterile products
- Sterile Presentations
Workshop 3: Focus on sterile products - How to prepare a dossier and prepare for an inspection
- Sterile Presentations
- Workshop: Inspections
- Inspections Presentations
Workshop 4: Inspection of manufacturing sites: Chemical products
- Inspections Presentations
- Plenary Session
- Programme
- Counteract the counterfeiters, Strasbourg, 21-23 September
- Introduction
- Organising Committee
- Seminar Conclusions (Short version)
- Speakers
- Programme
- Speeches & Presentations
- XpoPharm 2005, Seoul, Rep of Korea, 1-2 September
- Programme
- Final Symposium Programme
XpoPharm 2005, Seoul, Rep of Korea, 2 September 2005
- Final Symposium Programme
- Programme
- OMCL Information Day, 27 May
- Programme
- OMCL Programme
OMCL Information Day Programme
- OMCL Programme
- Proceedings
- OMCL Info Day Proceedings
Proceedings of the OMCL Information Day
- OMCL Info Day Proceedings
- Presentations
- Session 1 Slides
Session 1: Organisation & Structure of the Network - Session 2 Slides
Session 2: Common programmes of supervision activities for the network
- Session 1 Slides
- Programme
- Alternatives to Whole Cell Pertussis Vaccine Potency Vaccine, 16 March
- Programme
- Pertussis Prog
Programme: Alternatives to whole cell pertussis vaccine potency assay
- Pertussis Prog
- Proceedings
- Pertussis vaccine PA proceedings
Proceedings of the symposium on Alternative to whole cell pertussis vaccine potency assay
- Pertussis vaccine PA proceedings
- Presentations
- General Intro
General Introduction: Whole cell pertussis vaccine quality control - Intro Talk
Alternatives: Humane and science-based improvements of whole cell pertussis vaccine quality control: An overview - Round Table Talk I
Policy of the Ph.Eur. for lot release of combined vaccines for human use. - Scientific Presentations
Scientific Presentations of data obtained with the Kendrick test & other alternatives - WHO Perspective
Potency testing of whole cell pertussis vaccine
- General Intro
- Programme
- Quality of homoeopathic products in the new European legislative framework, 15 February
- Programme
- List Participants Homoe
List of participants, Homoeopathy Symposium, 15 February 2005 - Prog Homoe Sympos
Programme Homoeopathy Symposium, 15 February 2005, Strasbourg, France
- List Participants Homoe
- Proceedings
- Homoeopathy Proceedings
Proceedings
Quality of homoeopathic products: Conference Proceedings, 15 February 2005, Strasbourg, France
- Homoeopathy Proceedings
- Presentations
- Session 1 General
Session 1: General European Regulatory Background - Session 2 Experience
Session 2: Experiences and viewpoint of national regulatory authorities and perspectives - Session 3 Future
Session 3: The future of homoeopathics in Europe
- Session 1 General
- Programme
- 2005 Proceedings Archive
- 2004
- 2004 Proceedings Archive
2005 Conference Proceedings - Quality on the Move: Dynamics of the European Pharmacopoeia, 4-6 October
- Programme
- List Participants Quality
Quality on the Move - List of Participants - Scientific Programme Quality
Scientific Programme Quality on the Move Conference, 4-6 October 2004, Budapest, Hungary
- List Participants Quality
- Proceedings
- Quality Proceedings
Quality on the Move: Conference Proceedings, 4-6 October 2004, Budapest, Hungary
- Quality Proceedings
- Presentations
- Quality Day 1 Session Ia
Day 1 Session Ia: Roles of the European Authorities - Quality Day 1 Session Ib
Day 1 Session Ib: Roles of the European Authorities - Quality Day 1 Session IIa
Day 1 Session IIa:Viewpoint of the Regulatory Authorities - EMEA Working Parties - Quality Day 1 Session IIb
Day 1 Session IIb:Viewpoint of the Ph.Eur. & its Partners, & Industry - Quality Day 2 Blood & Plasma
Day 2: Blood & Plasma Products Workshop - Quality Day 2 BSP
Day 2: Biological Standardisation Workshop - Quality Day 2 Cell & Gene
Day 2: Cell & Gene Therapy Products Workshop - Quality Day 2 Certification
Day 2: Certification Workshop - Quality Day 2 CRS BRP
Day 2: Pharmaceutical Reference Substances CRS/BRP - Quality Day 2 Excipients
Day 2: Excipients Workshop - Quality Day 2 Harmonisation
Day 2: International Harmonisation Workshop - Quality Day 2 Herbals
Day 2: Herbals Workshop - Quality Day 2 Impurities
Day 2: Impurities Workshop - Quality Day 2 Micro Tech
Day 2: Microbiological Techniques Workshop - Quality Day 2 Pharm Dosage Form & ST
Day 2: Pharmaceutical Dosage Forms & Standard Terms Workshop - Quality Day 2 Pharm Waters
Day 2: Pharmaceutical Waters - Quality Day 3 Session I
Day 3 Session I: Conclusions & Action Plan for the Future - Recommendations from the Industry - Quality Day 3 Session II
Day 3 Session II: Perspectives for the WHO, Int. Harmonisation & the 6th Edition
- Quality Day 1 Session Ia
- Programme
- Serological Potency Tests for Diphtheria and Other vaccines, 6-7 October
- Programme
- List of Participants
Serological Potency Tests Symposium - List of Participants - Scientific Programme Serological
Scientific Programme Serological Potency Tests for Diphtheria and Other Vaccines, 6-7th October 2004, Budapest, Hungary
- List of Participants
- Proceedings
- Diphtheria Proceedings
Serological Potency Tests for Diphtheria and Other Vaccines Conference Proceedings, 6-7th October 2004, Budapest, Hungary
- Diphtheria Proceedings
- Presentations
- Session I
Session I: Alternative to Challenge Assays in Animals for Vaccines Control - Session II
Session II: Perspectives for Combined Vaccines Control - Session III
Session III: Conclusions & Action Plan
- Session I
- Programme
- 40th Anniversary European Pharmacopoeia 15 June
- Programme
- Programme
Programme Official Ceremony 40th Anniversary European Pharmacopoeia
- Programme
- Programme
- Process Analytical Technologies 3-4 May
- Programme
- PAT Programme
PAT Scientific Programme 3-4 May, Cannes, France
- PAT Programme
- Proceedings
- PAT Proceedings
Process Analytical Technologies Conference Proceedings, 3-4 May 2004
- PAT Proceedings
- Presentations
- PAT-Session I
PAT Day 1 Session I Role of the Pharmacopoeia Slides - PAT-Session II
PAT Day 1 Session II Test Methods to be Applied Slides - PAT-Session IIb1
PAT Day 2 Session IIb1 Test Methods to be Applied Slides - PAT-Session IIb2
PAT Day 2 Session IIb2 Test Methods to be Applied Slides
- PAT-Session I
- Programme
- 2004 Proceedings Archive
- 2003
- 2003 Conference Archive
2003 Conference Proceedings & Presentations - Microbiology Symposium, 5-6 May
- Programme
- Microbiology programme
Symposium scientific programme (5-6 May 2003, Langelinie Pavillon, Copenhagen, Denmark)
- Microbiology programme
- Proceedings
- Proceedings microbiology
Proceedings Microbiology Symposium, 5-6 May 2003
- Proceedings microbiology
- Presentations
- Microbiological sterilisation processes
Microbiological Sterilisation Processes. Slides session V - Microbiological Testing
Microbiological Testing of Raw Materials. Slides session IV - Microbiology Alternative New Control Methods
Slides session II - Development Culture Media
Slides session III - Microbiology International harmonisation
Slides session I - Microbiology Round table discussion
- Microbiological sterilisation processes
- Programme
- Foot
- Programme
- FMD programme
Symposium programme (17-18 March, EDQM Premises, Strasbourg, France)
- FMD programme
- Proceedings
- Foot and Mouth Disease
Foot and Mouth Disease proceedings, 17-18 March 2003
- Foot and Mouth Disease
- Presentations
- Introduction FMD
Introduction FMD vaccines, Slides session I - Requirements FMD efficacy
Requirements for a modern FMD vaccine: efficacy aspects to be dealt with, Slides session III - Requirements FMD vaccines
Requirements for a modern FMD vaccine: quality aspects to be dealt with, slides session II
- Introduction FMD
- Programme
- Cell and gene therapy Symposium, 24-25 February
- Programme
- Cell Gene Therapy Programme
Symposium on Standardisation and Quality Control Cell and Gene Therapy Products, Programme (24-25 February 2003), Hilton Hotel, Strasbourg, France
- Cell Gene Therapy Programme
- Proceedings
- Proceedings cell gene products
Standardisation and quality control cell and gene therapy products, 24-25 February 2003, Proceedings of the symposium.
- Proceedings cell gene products
- Presentations
- Cell Gene Developments
Latest Scientific Developments in Cell and Gene Therapy Products, Slides session I - Cell Gene Future
The Future, Slides session V - Cell Gene Regulatory
The Regulatory Issues, Slides session IV - Cell Quality Challenge
New Quality Challenges for Cell Therapy Products, Slides session II - Gene Quality Challenges
New Quality Challenges for Gene Therapy Products, Slides session III
- Cell Gene Developments
- Programme
- 2003 Conference Archive
- 2002
- 2002 Conference Archive
2002 Conference Proceedings & Presentations - 3Rs Symposium, 7-8 November
- Proceedings
- 3Rs proceedings
Symposium on 3Rs of the use of animals in the QC of vaccines, 7-8 November 2002, Proceedings of the symposium.
- 3Rs proceedings
- Presentations
- 3Rs future developments
Symposium on 3Rs of the use of animals in the QC of vaccines, 7-8 November 2002, Slides session 4 - 3Rs implementation needs practical aspects
Symposium on 3Rs of the use of animals in the QC of vaccines, 7-8 November 2002, Slides session 3 - 3Rs implementation regulatory
Symposium on 3Rs of the use of animals in the QC of vaccines, 7-8 November 2002, Slides session 2 - 3Rs regulatory scientific background
Symposium on 3Rs of the use of animals in the QC of vaccines, 7-8 November 2002, Slides session 1
- 3Rs future developments
- Proceedings
- Excipients, 4-5 April
- Proceedings
- Excipients proceedings
Excipients: Classical requirements and functionality related testing
- Excipients proceedings
- Proceedings
- ETIF
- Presentations
- ETIF MSJ
Farmacopea europea 4a Edicion: Que novedades presenta?ETIF 21-24 October 2002. Buenos Aires Argentina - ETIF CC
La farmacopea europea al nivel mundial: procedimiento de certificacion de conformidad y programa de trabajo del Pharmacopoeial Discussion group (PDG) ETIF 21-24 October 2002. Buenos Aires Argentina
- ETIF MSJ
- Presentations
- 2002 Conference Archive
- 2001
- Equine Influenza Vaccine, 10-11 December, Budapest, Hungary
- Proceedings
- Proceedings Equine
Quality control of equine influenza vaccines. Proceedings of the Workshop.
- Proceedings Equine
- Proceedings
- Certification of Suitability - New developments, 8-9 November, Athens, Greece
- Pestavirus Contamination of bovine sera and other bovine virus contamination, 29-30 March, Paris, France
- Future face of the European Pharmacopoeia, 8-9 February, Cannes, France
- Certification of TSE risk products, 11 January, Strasbourg, France
- Equine Influenza Vaccine, 10-11 December, Budapest, Hungary
- 2000
- 1999
- Beyond Biologicals 2000: Challenge for Quality Standards in an evolving field, 27-29 September 1999, Strasbourg, France
- Proceedings
- Biologicals Beyond 2000, 27-29 September
Challenges for Quality Standards in an Evolving Field
- Biologicals Beyond 2000, 27-29 September
- Proceedings
- Certification of Suitability: New aspects of the Procedure, 11-12 November 1999, Berlin, Germany
- 1- Proceedings
- Certification of Suitability of Monographs of the European Pharmacopoeia, 11-12 November
New aspects of the procedure: How to prepare your dossiers
- Certification of Suitability of Monographs of the European Pharmacopoeia, 11-12 November
- 1- Proceedings
- Beyond Biologicals 2000: Challenge for Quality Standards in an evolving field, 27-29 September 1999, Strasbourg, France
- 1998
- 1997
- 1996
- Other interesting events
- HelpDesk EDQM HealthCare European Pharmacopoeia & PDG Certification OMCL Activities & Guidelines Publications, Products Events organised by the EDQM Other Spécifiques
- Other EDQM HealthCare European Pharmacopoeia & PDG Certification OMCL Activities & Guidelines Publications, Products Events organised by the EDQM HelpDesk Spécifiques
- Spécifiques EDQM HealthCare European Pharmacopoeia & PDG Certification OMCL Activities & Guidelines Publications, Products Events organised by the EDQM HelpDesk Other
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