The EDQM (Council of Europe) is a key European Organisation involved in Harmonisation & Co-ordination of Standardisation, Regulation & Quality Control of Medicines, Blood Transfusion, Organ Transplantation, Pharmaceuticals and Pharmaceutical Care.
Vous pouvez télécharger le plugin flash permettant de visualiser cette animation à l'adresse suivante : http://www.macromedia.com/go/getflashplayer_fr
The European Directorate for the Quality of Medicines & HealthCare protects and promotes public and animal health in Europe. You can find out what's new, information about the EDQM and how to contact us.
Discover the EDQM activities on blood transfusion, organ transplantation and the safe and appropriate use of medicines. Learn about the news and general information on the activities.
Better understand the work of the European Pharmacopoeia and learn how to participate in the European Biological Standardisation Programme.
A major tool for guaranteeing the quality of substances for pharmaceutical use in the context of developing world trade. Discover the news and general information, how to submit new applications, revisions & renewals, how to apply for technical advice & one to one meeting and be informed about its legal status & background and inspection.
Since 1994, several coordinated European control programmes have been set up. These activities are covered by the Official Medicines Control Laboratories Network (OMCL Network), including quality assurance activities. Programmes such as proficiency testing studies (PTS) are also organised by the EDQM.
Discover the full range of publications, reference standards and services provided by the EDQM: the European Pharmacopoeia 6th Edition and other publications. EDQM Reference Standards and WHO ISA Standards. CombiStats and other services.
Pharmeuropa 21.1 January 2009
(05/01/09) List of contents now available under 'Downloads'.
For more information on how to order, please click below.
OCABR Human Biologicals
2008 Product Specific Guidelines and EC Procedures
(8/12/08) The procedures and guidelines are now available and are in force as of January 2009.
Human Biologicals (OCABR)International Harmonisation: Pharmacopoeial Discussion Group
(17/11/08) The last meeting of the PDG was held in Brussels, Belgium.
International HarmonisationHeparin: a new capillary electrophoresis method
(7/11/08) A new capillary electrophoresis method enabling baseline separation between heparin and OSCS.
News and General InformationPharmeuropa 21.1 January 2009
(05/01/09) List of contents now available under 'Downloads'.
For more information on how to order, please click below.
OCABR Human Biologicals
2008 Product Specific Guidelines and EC Procedures
(8/12/08) The procedures and guidelines are now available and are in force as of January 2009.
Human Biologicals (OCABR)International Harmonisation: Pharmacopoeial Discussion Group
(17/11/08) The last meeting of the PDG was held in Brussels, Belgium.
International HarmonisationHeparin: a new capillary electrophoresis method
(7/11/08) A new capillary electrophoresis method enabling baseline separation between heparin and OSCS.
News and General Information
7 allée Kastner, CS 30026, F67081 Strasbourg, France - Tel. +33 (0)3 88 41 30 30 - Fax +33 (0)3 88 41 27 71
Created by 2exVia with MasterEdit®