Product Risk Management Under ISO 14971 and FDA-ICH Q9 - Webinar By GlobalCompliancePanel 2012
08 Feb 2012
Webinar
Key Topics
The Master Validation Plan
Verification or Validation -- Recent regulatory expectations
When and How to Use DQ, IQ, OQ, PQ
Product V&V versus Process / Equipment V&V
The 11 Elements of the Software VT&V "Model"
Using the Risk Management tools of ISO 14971 and ICH Q9
Avoid recent "horror stories" and multimillion dollar fines
Who should Attend
Regulatory Affairs, Senior management, Production, Quality Assurance, All personnel involved in verification and/or validation planning, execution and documentation, Engineering and including Software.
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Important
Please, check "Product Risk Management Under ISO 14971 and FDA-ICH Q9 - Webinar By GlobalCompliancePanel" official website for possible changes, before making any traveling arrangements
Event Categories
Health & Medicine: Healthcare, Medical device, Pharma
