Presented on Tuesday, October 25, 2022

Download this informative co-hosted presentation reviewing insights and trends from the last five years on the top reasons regulated manufacturers receive 483 observations and warning letters and the 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
Speakers:

Sam Klooster

VP of Software, SIMCO Electronics

Jerry Chapman

Senior GMP Quality Expert, Redica Systems

If you have any questions or comments, please do not hesitate to contact someone on our team at events@redica.com.