USDA’s New Proposed Rule for Bioengineered (GMO)

Pre Recorded

  • 60 minutes

USDA Establishing the National Bioengineered Food Disclosure Standard

The USDA recently unveiled its long-awaited proposed GMO disclosure rule, the National Bioengineered Food Disclosure Standard, which provides food companies with guidance about how to label products made with genetically modified ingredients. This important proposed rule implements the National Bioengineered Food Disclosure Law of 2016 and will impact most food companies and their products. You should attend to find out how it will impact your product labeling and marketing.

Join this session with regulatory consultant, Norma Skolnik, where she will help you understand the key requirements of the National Bioengineered Food Disclosure Proposed Rule – such as the ingredients subject to disclosure, the acceptable labeling methods, GMO labeling symbols, thresholds and exemptions, timelines and more.

Session Highlights:

  • The presentation will help the attendee understand the requirements of the National Bioengineered Food Disclosure Proposed Rule.

  • Ingredients subject to Disclosure

  • Acceptable Labeling Methods of Disclosure

  • GMO Disclosure symbols that may be Used.

  • Thresholds of bioengineered foods and exemptions

  • Timelines for Implementation of the Proposed Rule.

Why You Should Attend:

A federal law was passed last year that preempts state laws, but there are still some unresolved issues that will be addressed in this webinar. This presentation will show you how to effectively label products with GMO ingredients and still comply with regulatory requirements.

Who Should Attend:

  • Regulatory managers and regulatory associates, Marketing managers, Product managers in the Food industry

  • Food product manufacturers, distributors and packers.

  • Anyone involved with Food product labeling and marketing

  • Food Director
  • Quality Assurance Personnel
  • Quality Control Personnel

*You may ask your Question directly to our expert during the Q&A session.
** You can buy On-Demand and view it as per your convenience.

Norma Skolnik

Norma Skolnik

Norma Skolnik is currently a Regulatory Consultant with over 35 years of regulatory experience working with the pharmaceutical and dietary supplement industries. She was Director of Regulatory Affairs for the Americas for Cadbury Adams and Director of Regulatory Affairs for the Adams division of Pfizer before that. Prior to that she was Associate Director of Regulatory Affairs for the Warner-Lambert company and Associate Director Regulatory Affairs at American Home Products Whitehall-Robbins Division.

No Reviews Found

Want to attend in a Group? Call 844-810-1151 and Save upto 50%

  • $164.00

  • $164.00

  • $164.00

  • $259.00

  • Total : $00.00

Share this course with a friend

We Also Recommend

Food Safety and Pharmaceuticals

FDA Trends on Mandatory Food Recall Management

Pre Recorded
60 minutes

Food Safety and Pharmaceuticals

FDA FSMA Preventive Controls: Cross Contact and Contact...

Pre Recorded
60 minutes


Get Notified about News, Webinars, Community & More