Book Online Tickets for USDA New Proposed Rule on BioEngineered , Palo Alto. Attend this webinar to learn how to be fully compliant with the USDA Final Rule on Bioengineered Food Disclosure, disclosure requirements in product labeling; disclosure options available to food manufacturers and distributors; symbols to be used and

USDA New Proposed Rule on BioEngineered (GMO) Food Disclosure

 

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About The Event

Attend this webinar to learn how to be fully compliant with the USDA Final Rule on Bioengineered Food Disclosure, disclosure requirements in product labeling; disclosure options available to food manufacturers and distributors; symbols to be used and graphic requirements; and the timelines for compliance.

Why Should You Attend:

You will learn how to be fully compliant with the USDA Final Rule on Bioengineered Food Disclosure. It is essential that food professionals understand which foods the USDA has listed as bioengineered and what firms are exempt from the Bioengineered Disclosure Rule.

After attending this webinar, you will know what food products are impacted by the new rule, and what food products are exempt. You will also be able to correctly label bioengineered/GMO (Genetically Modified) foods and non-GMO foods. Understanding the timelines for compliance is essential to ensuring your organization complies with the final rule in time to avoid regulatory enforcement actions.

Areas Covered in the Webinar:

  • Review list of bioengineered foods
  • Understand who is exempt from the bioengineered disclosure rule
  • Incidental additivities
  • Disclosure requirements in product labeling
  • Disclosure options available to food manufacturers and distributors
  • Symbols that are to be used and graphic requirements
  • Electronic or digital link disclosure
  • Small food manufacturers
  • Timelines for bioengineered food disclosure standard compliance

Who Will Benefit:

  • Regulatory Affairs
  • Marketing managers
  • Product Manager
  • Labeling managers

Instructor Profile:

Kelly Thomas

Kelly Thomas
Vice President, Americas Quality Operations

Ms. Thomas has over two decades of cGMP hands-on industry experience in both pharmaceutical and medical device manufacturing operations. Her experience covers all Quality Systems; as well as, all areas of validation; including, process/product validation, facilities validation, CSV and 21 CFR Part 11, test method validation, equipment/automated processes and cleaning validation.

Utilizing strategic thinking, risk-based approaches, and Lean principles, she has demonstrated success in steering and managing complex projects within the pharmaceutical and medical device industries.

 

 

Refund Policy

Registrants may cancel up to two working days prior to the course start date and will receive a letter of credit to be used towards a future course up to one year from date of issuance. ComplianceOnline would process/provide refund if the Live Webinar has been cancelled. The attendee could choose between the recorded version of the webinar or refund for any cancelled webinar. Refunds will not be given to participants who do not show up for the webinar. On-Demand Recordings can be requested in exchange.

Webinar may be cancelled due to lack of enrolment or unavoidable factors. Registrants will be notified 24hours in advance if a cancellation occurs. Substitutions can happen any time.

 

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