Topics
- Pivotal events that shaped laws in US and scope of FDA actions
- Food and drug oversight
- Consequences of noncompliance
- GMP vs. cGMP
- Emphasis on education and decision-making
- Building a culture of compliance
- Avoiding over-reliance on metrics
- Training, memory retention, and accountability
Who should Attend
Attendees with responsibilities in manufacturing, packaging or distribution of pharmaceutical products (e.g. Quality Assurance, Packaging, Operations, Planning).
