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:
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.