Understanding the Implications of FDA 483s and Actions to Avoid Further Regulatory Actions 2015 is a webinar that covers topics such as:
- Areas of focus during audits
- FDA regulatory actions based on deficiencies cited
- Actual case studies showing how poor management responses can carry implications for further regulatory action
- Recommended practices for addressing FDA 483
Understanding the Implications of FDA 483s and Actions to Avoid Further Regulatory Actions 2015 is intended for attendees involved or interested in:
- Quality Control
- Quality Assurance
- Validation
- Manufacturing
- Regulatory Compliance
- Production
- Management
- Laboratory Operations
