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Certification of Suitability to the Monographs of the European Pharmacopoeia: News & General Information

Certification Monthly Report of Activities

(16/02/12) The Certification of Substances Division (DCEP) will publish on a monthly basis, a report containing some relevant figures relating to its main activities. January 2012 Certification Monthly Report

How to communicate with EDQM Certification Division

(15/02/12) In order to facilitate communication between the EDQM Certification Division (DCEP) and applicants and also to clarify the ways to send documentation, the DCEP has prepared a guideline that underlines the different possibilities for communication being proposed to companies. Please read ‘Communication with EDQM Certification Division’ / PA/PH/CEP (11) 70 for more information.

CEP Suspensions

a) Following inspection of the manufacturing site(s):

 

Date Substance name CEP Number
08/02/12  Quinine hydrochloride CEP 2005-114
08/02/12  Quinine sulfate CEP 2005-117
08/02/12  Digoxin CEP 2009-281
08/02/12  Reserpine CEP 2010-041
08/02/12  Colchicine CEP 2011-016
07/02/12  Erythromycin CEP 2009-267
07/02/12  Trimetazidine dihydrochloride CEP 2007-245
20/12/11  Azathioprine CEP 2001-341
20/12/11  Ticlopidine Hydrochloride CEP 2003-066
20/12/11  Haloperidol CEP 2003-206
20/12/11  Risperidone CEP 2004-135
20/12/11  Diphenoxylate Hydrochloride CEP 2005-084
20/12/11  Nifuroxazide CEP 2006-074

04/11/11

 Isosorbide mononitrate, diluted

CEP 2002-104

04/11/11

 Protamine sulfate

CEP 2000-162

06/10/11  Oxytetracycline Dihydrate CEP 2002-211
06/10/11  Oxytetracycline Hydrochloride CEP 2002-070
06/10/11  Oxytetracycline Hydrochloride

CEP 2001-125

 

 

b) Due to a failure to comply with a declaration of willingness to be inspected and/or to operate according to EU GMP (e.g. refusal, of inspection, reconstruction/restoration of site(s), to achieve GMP level, and temporary closure):

 

Date Substance name CEP Number

20/12/11

Troxerutin

CEP 2006-153

15/09/11

Theophylline

CEP 1998-09


c) Upon request from the holder, due to a temporart inability to produce the API under the approved conditions

Date Substance name CEP Number
    None  

 

CEP Withdrawals

a) As a result of an inspection of the manufacturing site(s):

 

Date Substance name CEP Number

08/02/12

  Quinine sulfate

CEP 2009-387

08/02/12

Quinine hydrochloride

CEP 2010-069

15/09/11

Paclitaxel

CEP 2008-005

 

b) Due to a failure to fulfill the requirements of the CEP procedure with regards to updating the application and complying with GMP:

 

Date Substance name CEP Number

12/09/11

Tiamulin hydrogen fumarate for veterinary us

CEP 2007-008

12/09/11

Ribavirin

CEP 2009-257

 

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