Understanding the Implications of FDA 483s and Actions to Avoid Further Regulatory Actions 2015
10 Sep 2015
Webinar
Description
Topics
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
Who should Attend
Attendees involved or interested in:
Quality Control
Quality Assurance
Validation
Manufacturing
Regulatory Compliance
Production
Management
Laboratory Operations
Past Events
Understanding the Implications of FDA 483s and Actions to Avoid Further Regulatory Actions 2015 - 10 Sep 2015, Webinar (54027)
Important
Please, check "Understanding the Implications of FDA 483s and Actions to Avoid Further Regulatory Actions" official website for possible changes, before making any traveling arrangements
