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What's New at FDA  Members only

What's New at EMA Members only

What’s New at MHLW Members only

August 2010

20 Aug 2010 US FDA Proposes Withdrawal of Low Blood Pressure Drug Because Required Post-Approval Studies That Verify the Clinical Benefit of the Drug ...
20 Aug 2010 U.S., Ukraine Agree to Share Standards for Quality of
20 Aug 2010 Czech State Institute For Drug Control Issues Questions and Answers On Sunset Clause
20 Aug 2010 Chinese Commissioner Shao Mingli meets Commissioner of the U.S. Food and Drug Administration
13 Aug 2010 Relocation of Britain's MHRA head office
11 Aug 2010 137th session of the European Pharmacopoeia Commission
11 Aug 2010 European Medicines Agency / US Food and Drug Administration joint GMP inspection pilot programme. General principles
04 Aug 2010 US FDA Issues Assessments of the 510(k) Program and Use of Science in Decision-Making


July 2010

28 Jul 2010 Britain's MHRA Business Plan 2010 and Corporate Plan 2010-15 published
27 Jul 2010 Regulation of advanced therapy medicinal products in the UK
23 Jul 2010 Britain's MHRA Publishes New Enforcement Strategy
20 Jul 2010 European Medicines Agency publishes policy on communicating safety issues for human medicines
19 Jul 2010 Generic substitution appears to have increased competition in the Finnish pharmaceutical market
19 Jul 2010 Britain's Heads of Medicines Agencies drafts strategy 2011-15 consultation
15 Jul 2010 European Medicines Agency launches new website
09 Jul 2010 European Medicines Agency and European Commission start reflection process on way forward for the Agency and the network
09 Jul 2010 Britain's MHRA Annual Report and Accounts 2009/10
09 Jul 2010 Health Canada Publishes Draft Guidance Document - Labelling of Pharmaceutical Drugs for Human Use
07 Jul 2010 Danish Medicine's Agency Publishes Notification to Medicines Manufacturers About Reduced Testing of Starting Materials
07 Jul 2010 Eighth supplement to the 6th Edition European Pharmacopoeia takes effect



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