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March 2012

20 Mar 2012 US FDA Amends Labeling Requirements in 21 CFR Part 211
12 Mar 2012 EudraLex - Volume 2 - Pharmaceutical Legislation Notice to applicants and regulatory guidelines medicinal products for human use.
12 Mar 2012 US FDA Issues DTC Television Ad Guidance
09 Mar 2012 British MHRA's Red Tape Challenge – medicines regulations in the spotlight
08 Mar 2012 US could bring more common drugs over the counter
07 Mar 2012 US FDA: Keeping The Focus on Scientific Integrity
07 Mar 2012 Taiwanese FDA Explains the Rules on Processing Marketed Products that Fail the Random Inspection
06 Mar 2012 International collaboration on good manufacturing practice inspections expanded
05 Mar 2012 New PIC/S Recommendation: Recommended Model for Risk-Based Inspection Planning in the GMP Environment
02 Mar 2012 ICH E2C(R2) reaches Step 2 of the ICH Process
01 Mar 2012 Korean FDA's Main Tasks of 2012
01 Mar 2012 Global drug industry tightens anti-corruption code
01 Mar 2012 Chinese SFDA issues the 2011-2015 Work Plan for Electronic Supervision of Drugs

 

February 2012

29 Feb 2012 European Medicines Agency launches call for expression of interest from healthcare professional organisations
29 Feb 2012 European Medicines Agency increases public information on conflicts of interest of experts and management
28 Feb 2012 Vietnam study finds bribes dominate medicine prices
28 Feb 2012 Yin Li appointed as Party Secretary and Commissioner of Chinese SFDA
24 Feb 2012 US Biologics Center Annual Report FY 2010 : Innovative Technology Advancing Public Health
24 Feb 2012 Britain's MHRA Publishes 2011 Annual Report
22 Feb 2012 European Medicines Agency releases good pharmacovigilance practice modules for public consultation

 

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