This training offers a detailed, step-by-step guide to the FDA’s final rule repealing the use of FD&C Red No. 3 in food (including dietary supplements) and ingested drugs. Participants will learn about the regulatory background, compliance deadlines, actionable reformulation strategies, and the legal and financial risks for non-compliance. Real-world case examples and targeted compliance checklists are included to help food, supplement, and pharmaceutical stakeholders meet the new requirements and avoid costly regulatory penalties.
In this course you will learn the following:
* Summarize the regulatory changes regarding FD&C Red No. 3.
* Identify key compliance deadlines and requirements.
* Understand the process and standards for objections and hearings under the FD&C Act.
* Implement actionable steps to ensure compliance with the delisting of FD&C Red No. 3.
* Recognize the legal and financial consequences of non-compliance.
