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Regulatory Guidance

EMEA

European Medicines Agency (EMEA) Guidelines

This page provides access to regulatory guidance and other resources that are generally available from web sites operated and maintained by other organizations.

Documents which have been considered by the Committee for Human Medicinal Products or the Committee for Veterinary Medicinal Products, in consultation with the European commission and the competent authorities of the Member States, to assist applicants for a marketing authorisation.

New regulatory guidance and other resources for toxicology are now available.

Note: these links take you directly to the documents on the EMEA web site. Please click here to contact us and let us know if you have problems accessing them.


Title   Type Posted
  Concept Paper on the Development of a CHMP Guideline on Non-Clinical Testing for Concept Paper June 2005

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EMEA/CPMP/SWP/110180/04


  Guideline on Requirements for Vaccine Antigen Master File (VAMF) Certification Guideline (Revised) June 2005

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EMEA/CPMP/4548/03/Final/Rev 1


  Reflection paper on the Assessment of the Genotoxic Potential of Antisense Oligodeoxynucleotides Reflection Paper February 2005
CHMP/SWP/199726/2004
  Guideline on Active Substance Master File Procedure Guideline June 2002

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EMEA/CVMP/134/02 Rev 1


The European Medicines Agency (EMEA) Committee for Human Medicinal Products (CHMP), EU published (21 April 2005) QWP Guideline on Active Substance Master File procedure revision 1. The updated guidance was adopted at the April 2005 meeting of CHMP.

http://www.emea.eu.int/pdfs/human/qwp/022702en.pdf

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