Tougher U.S. FDA cGMP Compliance Audits - When You're Not Ready 2015
25 Nov 2015
Webinar
Key Topics
Avoid complacency from past "good" FDA/ ISO auditing
Learning Objectives
How to respond now – where to shift focus first
The desired response
How to address known problem areas during an Audit
Where to direct scarce resources; A risk-based phased approach
Maintain ‘the edge’
Prove ‘in control’
Who should Attend
QA Personnel
Senior Management in Drugs, Devices, Biologics, Dietary Supplements
R&D Staff
RA Personnel
Production Staff
Engineering Professionals
Consultants
Operations Professionals
Past Events
Tougher U.S. FDA cGMP Compliance Audits - When You're Not Ready 2015 - 25 Nov 2015, Webinar (13853)
Tougher U.S. FDA cGMP Compliance Audits - When You`re Not Ready 2026
Important
Please, check "Tougher U.S. FDA cGMP Compliance Audits - When You`re Not Ready" official website for possible changes, before making any traveling arrangements
Event Categories
Business: Quality assurance
Education: Training
Health & Medicine: Nutrition, Pharma, Wellness and fitness
