The Insider’s Guide to Audit Readiness

[webinar] "The Insider’s Guide to FDA Audit Readiness"
Presented on Tuesday, October 25, 2022

Watch this informative 1-hour co-hosted presentation reviewing insights and trends from the last five years on the top reasons regulated life sciences manufacturers receive 483 observations and warning letters from the FDA.

Speakers:
- Sam Klooster, VP of Software, SIMCO Electronics
- Jerry Chapman, Senior GMP Quality Expert, Redica Systems

Here's what you'll learn:
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