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What's New at EMA Members only

What’s New at MHLW Members only

August 2009

07 Aug 2009 Consultation: Draft Documents for Drug Good Manufacturing Practices (GMP) Inspection Program (GUI-0001 related)
07 Aug 2009 Consultation: Draft Documents for Drug Good Manufacturing Practices (GMP) Inspection Program
06 Aug 2009 FDA Commissioner Sets Out Vision on Enforcement to Support Public Health
03 Aug 2009 Health Canada Publishes the Following Documents
03 Aug 2009 FDA, European Medicines Agency Launch Good Clinical Practices Initiative
02 Aug 2009 Dutch Medicines Evaluation Board Publishes Authorisation of medicinal products in the first half of 2010
01 Aug 2009 August Human Medicines Highlights

 

July 2009

31 Jul 2009 The ICH Quality Implementation Group on Q8-Q9-Q10 has released a new set of Q&As that were signed in Yokohama, Japan, June 6-11.
31 Jul 2009 ICH Quality Implementation Group on Q8_Q9_Q10_QandA
20 Jul 2009 The ICH Quality Implementation Group on Q8-Q9-Q10 has released a new set of Q&As that were signed in Yokohama, Japan, June 6-11.
18 Jul 2009 China's Medicine Watchdog Launches Pharmaceutical Safety Program
17 Jul 2009 China launches more special programs to ensure drug safety
13 Jul 2009 FDA Issues Draft Guidance for Industry on Drug Anticounterfeiting
10 Jul 2009 Annual Report of the European Medicines Agency 2008
08 Jul 2009 Temporary cessation of the working process in the Bulgarian Drug Agency in August 2009
07 Jul 2009 Noted Food Safety Expert Michael R. Taylor Named Advisor to FDA Commissioner
03 Jul 2009 Implementation of the Variations Regulation - EU
03 Jul 2009 Implementation of the Variations Regulation - EU_2
03 Jul 2009 Guidance for coordination of GCP inspections
03 Jul 2009 New Zealand Publishes Outcome of Consultation on the proposed update to the Code of Good Manufacturing Practice for Manufacture and Distribution ...

 

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