News

04/04/2012 New FDA Guidance for Medical Devices	21/02/2011 China SFDA issues new GMPs version	14/07/2009 Training course
16/02/2012 Use of Heparin in drugs and medical devices	19/01/2011 New Annex 11 and new Chapter 4 (Documentation) of EU GMP	23/06/2009 Inspections from EU and USA Agencies to China API producers: Results a...
03/02/2012 Changes in Spanish pharmacovigilance legislation and new EMA pharmacov...	18/01/2011 New FDA draft Guidance on Electronic Sources on clinical investigation...	16/06/2009 New Q&A document on implementation of ICH Q8, Q9 and Q10 guidances pri...
07/06/2011 TDV will attend CPHI-China 2011	23/07/2010 FDA Inspection - Evaluation of 21 CFR Part 11 compliance	16/06/2009 Updated Categories of Variations in the New Variations Regulation
28/02/2011 Chinese SFDA issues new GMP implementation roadmap	22/07/2010 Part 2 of EU GMP Guide Modified	03/06/2009 ASSOCIATED CAPSULES PVT. LTD. In India, audited by TDV on behalf of Fo...
25/02/2011 Comparative overview of the 2010 Chinese GMP, EU GMP and US GMP	20/07/2010 Evaluation of Warning Letters 2009	26/05/2009 TDV in CPhI Shanghai