Monthly Newsletter: Dietary Supplements
Certified Laboratories, Inc.
So The World Can Trust In What It Consumes?
- Supplement Groups React to RFK Jr. HHS Confirmation
- What Trump's Regulatory Freeze Could Mean for Regulated Industries
- 2025 Legal and Regulatory Outlook for Supplement Industry
- Omega-3 Supplements Slow Biological Aging, Study Suggests
- Global Supplements Market Projected to Grow to $259 billion by 2029
Join us in San Diego for the Sports & Active Nutrition Summit! Talk to our team about how our lab testing services can support your safety and quality programs!
Meet us at the Certified Laboratories stand in the Regatta Pavilion.
FAQ: The FDA’s Revocation of Red Dye 3 for Food and Ingestible Drug Use
The U.S. FDA has banned Red Dye 3 in food and ingestible drugs, including supplements.
- When does the ban take effect?
- How do I test my raw materials and products for Red Dye 3?
- What are alternatives to Red Dye 3?
We answer those questions and more in our FAQ!?
GMPs dictated in 21 CFR 111 have been in place for over a decade, but the FDA continues to issue numerous Warning Letters to the industry for a failure to comply.
EAS Consulting Group, a Certified Group company, is offering this virtual seminar to help supplement companies understand their requirements for compliance.
- Learn 21 CFR 111 and other key regulatory requirements.
- Get practical guidance on applying these rules at your facility.
- Receive coaching on FDA inspections to avoid Form 483.
- Participate in group sessions to demonstrate GMP knowledge.
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Key Update: FDA Hyper Focused on Method Validation/Verification
We've noticed a significant increase in instances of the U.S. FDA asking our customers for product-specific reports proving that their products were tested on validated analytical test methods.? ??
For that reason, Certified Laboratories now requires the completion of method validation and product-specific method verification to be performed on all prescription or over-the-counter (OTC) finished good products prior to the start of routine testing. ?
If this affects your products, please contact your Sales or Business Development team member, who can provide more information or connect you to our Innovation and Validation team experts.?
Webinar - The Role of Your U.S. Agent?
EAS Consulting Group, a Certified Group company, is offering a chance to discover how foreign companies can successfully enter the U.S. market by meeting critical FDA requirements with the support of a U.S. Agent.
In this complimentary webinar, you will learn practical strategies to manage establishment registrations, product listings, inspection preparation, and more –?all designed to streamline your path to regulatory compliance.
- Title: The Role and Value of a U.S. Agent
- Date: March 18, 2025
- Time: 1:00 PM (Eastern)
- Instructors: Victoria Pankovich and Lisa El-Shall
Feb. 19-21, San Diego, California
March 4-7, Anaheim, California
Booth #4381 Hall D