We invite you to join the South Florida Manufacturers Association Regulatory Committee as we examine the fundamental requirements for all QC laboratories subject to FDA inspection, recent trends from FDA inspection reports and enforcement actions. Learn from Dr. Jose Zayas how quality control and quality assurance personnel can monitor industry practices to stay “current” with FDA requirements (cGMPs and GLPs).
Speaker: Dr. Zayas has over 35 years of experience in operations, quality management, and research and development, specifically in antimicrobial molecules and products with an emphasis in dermatology and respiratory applications.
Co-Sponsor(s): the Regulatory and Quality Committee of the South Florida Manufacturers Association, Lean Enterprise Consulting, the American Society for Quality, and The Puerto Rico Manufacturers Association.
