Meeting Annual U.S. FDA cGMP Training Requirements - Webinar By GlobalCompliancePanel 2011
05 Oct 2011
Webinar
Key Topics
Avoid complacency from past "good" FDA / ISO compliance
Focus on key cGMP issues
The major 21 CFR issues in 111, 210 / 211, and 820
Developing the Annual Lesson Plan(s)
How to address known problem areas during cGMP training
Defect recognition
Monitor and maintain `the edge`
Stop unauthorized changes -- Prove `in control`
Who should Attend
QA, Senior management in Drugs, Devices, Biologics, Dietary Supplements, R&D, RA, Production, Engineering, Consultants; others tasked with project leadership responsibilities and Operations.
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Important
Please, check "Meeting Annual U.S. FDA cGMP Training Requirements - Webinar By GlobalCompliancePanel" official website for possible changes, before making any traveling arrangements
Event Categories
Education: Training
Health & Medicine: Healthcare, Medical device, Pharma
