USDA Final Genetically Modified Organism (GMO) Label Rule

Recorded Webinar | Dr. John Ryan | From: Aug 07, 2024 - To: Dec 31, 2024

Training Options & Pricing

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Recording     $229
DVD     $249
Recording + DVD     $389
Transcript (Pdf)     $229
Recording & Transcript (Pdf)     $379
DVD & Transcript (Pdf)     $389


Description

In order to provide consumers with trust in labeling, transparency, education, and other factors, If your product contains greater than 5% of ingredients that were bioengineered, product labeling must contain the appropriate mandatory labeling. This webinar will provide you and your staff with disclosure methods, implementation deadlines, labels, printed text, scanning information, web address, and text messaging designed to be sent directly to consumer mobile devices that disclose product GMO information.

Food manufacturers are required to “prominently’ display clear label information regarding the presence of bioengineered ingredients. The new rules are designed to provide consumers with clear information and consistently labeled products.

Understanding how the GMO Label Rules apply to your products is critical in order to avoid recalls.

Learning Objectives:-

  • Understand the Rules
  • Review Rule Definitions
  • Plan label change implementation immediately       
  • Compliance with mandatory deadlines based on company size
  • Know your label options
  • Understand the exemptions
  • Detectability Issues
  • Record-Keeping Requirements

Areas Covered:-

  • Basic Rule Requirements
  • Implementation and Compliance (voluntary and mandatory)
  • Determining Your Company Requirements and Plan
  • Analytical Testing and Validation
  • Responsibility for and Type of Disclosures
  • Placement of disclosure
  • Use of your company URL
  • Small and very small packaging
  • Bulk containers
  • And More

Background:-

The need for GMO labeling has been a hot topic for over 20 years.  Scientific inquiry regarding the safety of GMO products has generated more questions than have been answered and has added fuel to the controversy.

After extensive review and industry input, the National Bioengineered Food Disclosure Law) PL114-216) was signed into law in July 2016.  The rules impact many types of food including beer, dairy products, breakfast cereals, and others often not commonly associated with GMO ingredients by consumers.

Beginning in February 2019, food manufacturers, importers, and retailers must disclose the presence of ingredients or foods made from or containing genetically engineered ingredients when the bioengineered percentage exceeds 5 percent. 

Companies may disclose bioengineered ingredients and can use the USDA “Bioengineered”, and “Derived from Bioengineering” symbols, or text printed that includes “bioengineered food” or “contains bioengineered food ingredients”.

The National Bioengineered Food Disclosure Law) PL114-216) was signed into law in July 2016.

Why Should You Attend?

In order to provide consumers with trust in labeling, transparency, education, and other factors, If your product contains greater than 5% of ingredients that were bioengineered, product labeling must contain the appropriate mandatory labeling.  This webinar will provide you and your staff with disclosure methods, implementation deadlines, labels, printed text, scanning information, web address, and text messaging designed to be sent directly to consumer mobile devices that disclose product GMO information.

Food manufacturers are required to “prominently’ display clear label information regarding the presence of bioengineered ingredients.  The new rules are designed to provide consumers with clear information and consistently labeled products.

Understanding how the GMO Label Rules apply to your products is critical in order to avoid recalls.

Who will Benefit?

  • Food Retail and Restaurant Operations
  • CEOs, VP, and Director Level Personnel in food companies are impacted by the rules
  • Food Safety and Quality Team Members
  • Quality System Personnel
  • Labeling and packaging personnel
  • Operations and compliance personnel
  • Documentation, data, management analysis, and recall team members.