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 Master Verification and Validation Planning Under U.S. FDA CGMP ICH Q-series and ISO 13485-14971 Requirements
GlobalCompliancePanel
[March 21, 2012 - March 21, 2012]
Medical and Pharmaceuticals
Wilmington,
Delaware
[USA]
 Changes in the EU Medical Device Directives 2010 Modifications and the 2012 Recast of the MDD Directives
GlobalCompliancePanel
[March 13, 2012 - March 13, 2012]
Medical and Pharmaceuticals
Wilmington,
Delaware
[USA]
 DHF DMR DHR and the Technical File Design Dossier - Similarities and Differences
GlobalCompliancePanel
[March 7, 2012 - March 7, 2012]
Business Services
Wilmington,
Delaware
[USA]
 USFDA and EU Essentials of Drug Safety and Pharmacovigilance
GlobalCompliancePanel
[March 5, 2012 - March 7, 2012]
Medical and Pharmaceuticals
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Analytical Products
TBA
Mumbai,
Maharashtra
[India]
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Total 'Seminar' available now: 4 |
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