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What's New at EMA Members only

What’s New at MHLW Members only

January 2013

08 Jan 2013 ANZTPA: Description of a possible joint regulatory scheme for therapeutic products under ANZTPA

 

December 2012

28 Dec 2012 Malaysia Enacts New Drug Registration Guideline
21 Dec 2012 Health Canada Publishes Summary Report of Drug GMP Inspection Program
21 Dec 2012 India's National Vaccine Regulatory Authority Declared Functional Against WHO Assessment Indicators
21 Dec 2012 Health Dialogue between the Russian Federation and the EU on medicinal products: publication of the report "Cooperation in the field of ...
20 Dec 2012 ICH E2C(R2) Guideline reaches Step 4 of the ICH Process
20 Dec 2012 ICH S10 Guideline reaches Step 2 of the ICH Process
19 Dec 2012 European Medicines Agency reviews its operations and prepares for reorganisation in 2013
18 Dec 2012 European Medicines Agency’s Management Board endorses work programme 2013
17 Dec 2012 US Publishes Strategies for More Successful Drug Trials
14 Dec 2012 Chinese National Institutes for Food and Drug Control qualifies as WHO drug quality control laboratory
12 Dec 2012 U.S. and Canada Working Together To Provide Access to Needed Veterinary Drugs
12 Dec 2012 Order issued ensuring rights/safety of clinical trial subjects in India
11 Dec 2012 Chinese SFDA Commissioner Yin Li and Deputy Commissioner Bian Zhenjia meet with Assistant Deputy Minister of Health Canada
10 Dec 2012 Danish Health and Medicines Authority publishes New guideline: renewal of marketing authorisation for nationally authorised medicinal products
07 Dec 2012 Danish Health and Medicines Authority publishes Annual report on human tissues and cells 2011
06 Dec 2012 British MHRA publishes medicines reclassification guidance
04 Dec 2012 ICH Steering Committee revises the S1 Strategy
03 Dec 2012 U.S. court voids drug rep's conviction, cites free speech

 

November 2012

30 Nov 2012 Finnish Medicines Agency revises Regulation concerning clinical trials on medicinal products

 

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