IEH Academy

Food Copacker Approval & Oversight Program

Course details

Self-Paced eLearning

69.00

45 Min

Dr. Suf Alkhaldi

Partnering with a food copacker does not transfer legal responsibility for food safety or regulatory compliance. Under 21 CFR 117, brand owners remain accountable for approving, verifying, and documenting copacker performance within their supplier approval program.

This course examines FDA expectations, common compliance failures, and the oversight and documentation systems necessary to control risk and maintain regulatory compliance.

Benefits and Learning Objectives

After completing this course, participants will be able to:

  • Explain why FDA classifies copackers as suppliers under 21 CFR 117
  • Describe FDA requirements for copacker approval, audits, and ongoing oversight
  • Identify key components of an effective copacker food safety and quality system
  • Recognize common food safety, labeling, and allergen risks associated with copacker operations
  • Apply documentation, monitoring, and corrective action to support regulatory compliance
Screenshot three for course on Primary Food Contact Materials.

Agenda

  • Regulatory Basis: Copackers as Suppliers Under 21 CFR 117
  • Copacker Approval and Verification Requirements
  • Evaluating Copacker Food Safety and Quality Systems
  • Risk Areas: Food Safety, Labeling, and Allergen Controls
  • Documentation, Monitoring, and Corrective Action Practices

Who Should Attend?

  • Brand Owners and Private Label Companies
  • Quality Assurance and Food Safety Professionals
  • Regulatory and Compliance Personnel
  • Supplier Approval and Procurement Teams
  • Operations and Technical Managers Working with Copackers

Registration and Payment

To register for this course, please visit our training portal.

Dr. Suf Alkhaldi

Meet the Instructor

Dr. Suf Alkhaldi

Dr. Suf Alkhaldi joined IEH as the Senior Vice President of Technical Services in 2023. He earned his M.S. and Ph.D. in Microbiology and Cell Molecular Biology from Oklahoma State University. He also conducted a postdoctoral study in Rumen Microbiology in Animal and Dairy Science at the University of Georgia and served as the manager of the DNA Microarray Lab at Yerkes National Primate Research Center at Emory University.

Before joining IEH, Dr. Alkhaldi spent over two decades at FDA which has been characterized by his exceptional contributions to innovation and regulatory excellence. He began as a researcher and food outbreak investigator at the Center for Food and Applied Nutrition (CFSAN), focusing on developing cutting-edge methods for identifying pathogenic bacteria in food using molecular techniques. With over 29 peer-reviewed manuscripts, 14 reviewed papers and book chapters, and co-editing “The Bad Bug Book,” he demonstrated a strong commitment to knowledge-sharing and food safety. Dr. Alkhaldi has played an instrumental role in resolving the FDA’s 2008 pepper outbreak investigation.

Throughout his extensive career at FDA, Dr. Alkhaldi held various roles, including Project Manager, Supervisor, and Senior Science Advisor in the Office of the Chief Scientist. He actively participated in influential working groups and the FDA Funded Centers of Excellence, reinforcing his dedication to advancing microbiology and FDA drug policies. Adding to his accomplishments, Dr. Alkhaldi received over 20 FDA awards between 2000 and 2023.

Dr. Alkhaldi was selected to lead the Office of Safety within the Office of Regulatory Affairs (ORA). His exceptional leadership during the COVID-19 pandemic was evident as he led a team of 24 Industrial Hygienists and safety professionals. Their dedication ensured the safety of 5,000 FDA employees and provided support for 16 FDA laboratories, demonstrating his significant impact in fostering a safe and innovative regulatory environment within the FDA and the broader field of food microbiology.

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