The Insider’s Guide to FDA Audit Readiness
Presented on Tuesday, October 25, 2022
Download this informative 1-hour co-hosted presentation reviewing insights and trends from the last five years on the top reasons regulated manufacturers receive 483 observations and warning letters.
Speakers:
- Sam Klooster, VP of Software, SIMCO Electronics
- Jerry Chapman, Senior GMP Quality Expert, Redica Systems
What is covered:
Data intelligence behind the five key factors that can impact your company’s FDA compliance, including:
- Quality
- Audit Trails
- Digital/Electronic Signatures
- Access and Control
- Compliance and Validation
If you have any questions or comments, please do not hesitate to contact someone on our team at info@redica.com or +1 (844) 332-3320.