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  • Recommandation relative à la présentation des monographies de substances d'origine humaine ou animale - novembre 2010
    Recommandations relatives à la présentation des monographies de substances d'origine humaine ou animale (novembre 2010)
  • Setting global specifications for excipient standards and test methods
    The article below was first published in European Pharmaceutical Review, Volume 6, Issue 2 & 3 Setting Global Specifications for Excipient Standards and Test Methods Peter Castle, European Pharmacopoeia/Secretary to the Commission and Dankward Jäkel, European Pharmacopoeia/Scientific Officer
  • Report - EDQM Annual Report 2009 - June 2010
    The European Directorate for the Quality of Medicines & HealthCare (EDQM) is a directorate of the Council of Europe, the oldest European institution which, today, has 47 member states, representing 800 million citizens across Europe.
  • Rapport - EDQM Rapport annuel 2008 - juin 2009
    Comme chaque année, la publication du rapport annuel est l’occasion de nous tourner vers les 12 mois écoulés pour tirer le bilan de nos activités et réfléchir aux événements et réalisations de l’année.
  • Report - EDQM Annual Report 2008 - June 2009
    The activities of the European Directorate for the Quality of Medicines & HealthCare are described in terms of its 5 main areas of responsibility. • The European Pharmacopoeia, including reference substances and preparations, the biological standardisation programme, publication and communications activities and international relations • The Procedure for Certifi cation of Suitability • The European network of Offi cial Medicines Control Laboratories (OMCLs) • Blood Transfusion and Organ Transplantation • Pharmaceuticals and Pharmaceutical Care The year 2008 saw the successful integration of new activities, in the areas of combating counterfeits and of pharmaceutical care, into the portfolio of the EDQM.
  • Technical guide for the elaboration of monographs for immunological human medicinal products, 2008
    Technical Guide for the elaboration of monographs on vaccines and other immunological human medicinal products
  • Report - EDQM Annual Report 2007 - June 2008
    The activities of the European Directorate for the Quality of Medicines & HealthCare are described in terms of its 5 main areas of responsibility. The European Pharmacopoeia, including publication and communications activities and international relations European Pharmacopoeia Department Communications and Public Relations Provision of reference substances and preparations Preparation and dispatching of samples Biological Standardisation Programme The Procedure for Certification of Suitability The European network of Official Medicines Control Laboratories (OMCLs) Blood Transfusion Organ Transplantation
  • Resolution - Certification of suitability to the monographs of the European Pharmacopoeia (revised version) - February 2007
    RESOLUTION AP-CSP (07) 1 (adopted by the Public Health Committee (Partial Agreement) (CD-P-SP) on 21/02/2007) - The Public Health Committee (Partial Agreement) (CD-P-SP) consisting, for the purposes of the Convention on the Elaboration of a European Pharmacopoeia, of delegations appointed by the Parties to the said Convention, namely the delegations of Austria, Belgium, Bosnia and Herzegovina, Bulgaria, Croatia, Cyprus, the Czech Republic, Denmark, Estonia, Finland, “the Former Yugoslav Republic of Macedonia”, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Montenegro, the Netherlands, Norway, Poland, Portugal, Romania, Serbia, Slovak Republic, Slovenia, Spain, Sweden, Switzerland, Turkey, United Kingdom and the European Union,
  • Rapport - EDQM Rapport annuel 2006 - juin 2007
    Comme chaque année, la publication du rapport annuel est l’occasion de nous tourner vers les 12 mois écoulés pour tirer le bilan de nos activités et réfléchir aux événements et réalisations de l’année.
  • Report - EDQM Annual Report 2006 - June 2007
    The activities of European Directorate for the Quality of Medicines are described in terms of its 3 main areas of responsibility: 1. the European Pharmacopoeia, including publication and communications activities, and international relations 1.1. European Pharmacopoeia Department 1.2. Communications and Public Relations 1.3. Provision of reference substances and preparations 1.4. Preparation and dispatching of samples 1.5. Biological Standardisation Programme 2. the procedure for Certifi cation of Suitability, 3. the European network of Official Medicines Control Laboratories (OMCLs). In 2006, pharmacopoeia authorities and licensing authorities all over the world showed growing interest in the work of the European Pharmacopoeia, Certification of Suitability and the network of Official Medicines Control Laboratories.