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March 2013

04 Mar 2013 Canada Publishes Information on Classification of Health Products at the Device-Drug Interface
01 Mar 2013 Tackling medication errors: European Medicines Agency workshop calls for coordinated EU approach

 

February 2013

28 Feb 2013 Chinese SFDA issues Opinions on Deepening Drug Evaluation and Approval Reform and Further Encouraging Drug Innovation
26 Feb 2013 British MHRA looking to appoint new Chief Executive
22 Feb 2013 British Annual report on regulation of medicines advertising published
20 Feb 2013 Industry and EU clash over medical devices regulation
16 Feb 2013 SFDA issues Technical Requirements for the Study of New Natural Medicines
12 Feb 2013 RPT-Slow approvals put India's drug trials industry at risk
07 Feb 2013 DG Health and Consumers and the European Medicines Agency renew confidentiality arrangement with Japan.
06 Feb 2013 EC establishes Draft Guidelines on the Formalized Risk Assessment For Ascertaining the Appropriate Good Manufacturing Practice For Exipients ...
06 Feb 2013 EC Publishes Draft Guidelines on the Principles of Good Distribution Practices for Active Substances for Medicinal Products for Human Use

 

January 2013

30 Jan 2013 New Members of the EMA Management Board appointed
30 Jan 2013 SFDA Launches Saudi Code of Ethics for Marketing of Pharmaceutical Products
22 Jan 2013 US FDA Releases GMP regulation for combination products
21 Jan 2013 British MHRA asks for views on new corporate plan
17 Jan 2013 Public consultation on the revision of EU Commission guidelines on Good manufacturing Practice Medicinal Products
16 Jan 2013 Dutch Medicines Evaluation Board in figures: 2012
10 Jan 2013 Chinese SFDA cracks down on illegal Internet pharmacy sales
10 Jan 2013 India publishes Guidelines For Good Distribution Practices For Pharmaceutical Products
08 Jan 2013 ANZTPA: Description of a possible joint regulatory scheme for therapeutic products under ANZTPA

 

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