Designing and Sustaining New and Existing Product Stability Testing Program is a seminar dedicated to the requirements of the FDA’s Drug Stability Guidelines that is stipulated for new, existing and modified drug products that have an existing or new IND or NDA submission.
Who should Attend
Attendees from Pharmaceutical, Biotechnology or Medical Device industries, including:
- Senior Management
- Quality Control Analyst and Management
- Shipping and Distribution Personnel
- Manufacturing Associates and Management
- Regulatory Affairs
- Stability Testing Department Personnel and Management
- Process Design Personnel and Management
- Quality Assurance Analyst and Management
- Drug Packaging Personnel and Management
Who Will Benefit:
- Quality Control Analyst and Management
- Senior Management
- Manufacturing Associates and Management
- Shipping and Distribution Personnel
- Stability Testing Department Personnel and Management
- Regulatory Affairs
- Quality Assurance Analyst and Management
- Process Design Personnel and Management
- Drug Packaging Personnel and Management
