Benchmark Your Food Safety Training Program: Results & Insights from the 2026 Global Food Safety Training Survey

April 13, 2026 by Alexis Ocampo

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Join this webinar to explore key findings from the Global Food Safety Training Survey, such as organizations with a strong training program are 12X more likely to have strong, consistent adherence to established protocols on the floor.  

As the most comprehensive research conducted on food manufacturer training, the data provides an opportunity to benchmark your employee training program with industry peers to identify your strengths & opportunities for improvement.  

Key takeaways: 

  • Dozens of data points to help guide improvement efforts in your training program 
  • Insights into best practices that can lead to better outcomes on the floor 
  • Quantifying the link between engaged employees & better performance 
  • How AI is impacting food safety training & how you can leverage AI in your programs 

  Join us for this deep dive into the research and how to apply the findings. Registrants will receive a complimentary copy of the Global Food Safety Training Survey Research Paper. 

 About the Speakers: 

Laura Dunn Nelson  

Culture Strategies Group 

Laura Dunn Nelson is a globally recognized food safety expert with 40+ years of experience designing and strengthening food safety, quality, & culture programs across manufacturing, processing, packaging, food service, & retail. She has served on multiple GFSI technical working groups—including Food Safety Culture and Storage & Distribution—and is widely known for helping organizations translate regulatory expectations into practical, culture‑driven execution. 

Bertrand Edmond  

Campden BRI 

For the past 30 years, Bertrand has been helping companies of all sizes from all parts of the agri-food chain not only survive but grow. He has taken part in numerous initiatives aiming to support businesses with respect to Quality, Safety, Efficiency, & Innovation. He is passionate about supporting the industry in the area of skills, knowledge, competency, culture, & continuing professional development. Bertrand holds a Master of Food Science & Technology and an MBA. 

For Medical Device Establishments, who must register?

Owners or operators of establishments involved in producing and distributing medical devices intended for the U.S. market must register annually with FDA and pay an annual registration fee.

What information is submitted for medical device establishment registration?

In addition to registering with FDA, most owners or operators of medical device establishments must also submit a list of all devices during their annual registration renewal.

  • U.S. Facilities
    • Initial importers must identify the manufacturers of the devices they are importing.
    • A device must be listed if they fall under the any of the following:
      • Contract Manufacturer
      • Contract Sterilizer
      • Manufacturer
      • Relabeler / Repackager
      • Remanufacturer
      • Reprocessor of Single Use Device
      • Specification Developer
      • U. S. manufacturer of export only devices

       

     

  • Non-U.S. Facilities
    • Must list devices, provide a U.S. Agent, and identify importers.

     

Who must provide medical device listings?

In most cases, all medical device establishments required to register with FDA must also submit a complete list of medical devices manufactured for commercial distribution in the U.S. market.

All facilities that fall under any of the following functions:

  1. Contract Manufacturer
  2. Contract Sterilizer
  3. Foreign Exporter
  4. Manufacturer
  5. Relabeler / Repackager
  6. Remanufacturer
  7. Reprocessor of Single Use Device
  8. Specification Developer
  9. U.S. manufacturer of export only devices

What information is submitted for a medical device listing?

Medical device establishments must list any medical device made in the establishment and the activities the device is meant for.

  1. Company function (activity)
  2. Device product code
  3. Proprietary names
  4. Importer information

What is a master file?

A Master File is a secure, confidential submission of proprietary product data to a regulatory agency, such as the U.S. Food and Drug Administration (FDA), Health Canada, or the National Medical Products Association (NMPA) in China.

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