Scientific and regulatory meetings

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Table of contents

Human

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Document(s) Language Status First published Last updated Effective Date
Work instructions for organisation of paediatric expert group meetings (English only) adopted 2012-11-29   2012-11-30
Standard operating procedure for organisation of the regulatory intelligence meetings (English only) adopted 2011-09-06   2011-09-05
Work instructions for handling of Article 29(1) referrrals to the Co-ordination Group for Mutual Recognition and Decentralised Procedures - Human (CMDh) (60-day procedure) by the CMDh secretariat (including Article 13 referrals for variations) (English only) adopted 2011-08-31   2011-08-30
Standard operating procedure on the organisation of Name Review Group meetings (English only) adopted 2011-04-18   2011-04-15
Standard operating procedure on the organisation of the monthly pre-CHMP teleconferences between the European Medicines Agency and the Directorate General for Health and Consumers’ of the European Commission (English only) adopted 2010-11-30 2013-07-29 2013-07-25
Standard operating procedure for evaluation of conflicts of interests of experts for involvement in Agency activities (English only) adopted 2006-08-22 2013-07-10 2013-07-10
Standard operating procedure for preparation and publication of Committee for Orphan Medicinal Products monthly report (English only) adopted 2007-10-15 2011-12-19 2011-12-20
Standard operating procedure on the organisation of Innovation Task Force briefing meetings (medicines for human / veterinary use) (English only) adopted 2006-10-30 2013-03-14 2013-03-15
Standard operating procedure for the organisation of European Medicines Agency Human Scientific Committees’ Working Party meetings with Patients' and Consumers' Organisations (PCWP) and Healthcare Professionals’ Organisations (HCPWP) (English only) adopted 2007-12-05 2015-02-18 2015-01-13
Standard operating procedure for organisation and management of ENCePP plenary meetings (English only) adopted 2010-11-18   2010-11-18
Work instructions for organisation of scientific-advice and protocol-assistance presubmission meetings (English only) adopted 2008-07-01 2013-06-24 2013-06-24
Work instructions for general dealings between SAWP secretariat and working parties, SAGs, committees and patients' organisations (English only) adopted 2009-11-24   2009-11-26
Work instructions for maintenance of rapid-alert/non-urgent-information (RA/NUI) contact points list and fax machine for RA/NUI use (English only) adopted 2008-12-05 2011-08-01 2011-07-29
Work instructions for organisation of Scientific Advice Working Party meetings (medicines for human use) (English only) adopted 2008-07-28 2013-06-11 2013-06-11

Veterinary

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Document(s) Language Status First published Last updated Effective Date
Work instructions for organisation of CVMP Working Party meetings (English only) adopted 2017-01-05   2016-12-15
Work instructions for Committee for Medicinal Products for Veterinary Use (CVMP) press release procedure and publication of documents adopted by CVMP (English only) adopted 2015-05-07   2015-05-01
Work instructions for tasks for processing scientific advice applications and organising meetings of the CVMP Scientific Advice Working Party (SAWP-V) (English only) adopted 2007-05-16 2015-06-12 2015-06-09
Standard operating procedure for CVMP MUMS/limited market classification procedure (English only) adopted 2010-10-25 2015-06-12 2015-06-12
Standard Operating Procedure for Requests for advice from CMD(v) to CVMP (English only) adopted 2008-01-16   2008-01-16
Standard operating procedure for review and approval of VICH guidelines by CVMP and its working parties (English only) adopted 2009-08-24 2015-09-02 2015-08-21