Reviewed and Approved by Shelly Blackwell, Senior Director of Dietary Supplements and Tobacco Services, EAS Consulting Group; and Tim Lombardo, Senior Director of Food Services, EAS Consulting Group 1-Minute Summary FDA regulations require you to qualify your...
Reviewed and Approved by Dean Cirotta, President – EAS Consulting Group & Executive Director of Regulatory Affairs – Certified Group 1-Minute Summary cGMPs require a thorough OOS investigation if your in-house or third-party lab produces an...
Reviewed and Approved by Dean Cirotta, President, EAS Consulting Group, a Certified Group company 1-Minute Summary Own Label Distributors (OLD) and Private Label Distributors (PLD) are responsible for ensuring cGMP compliance across all production phases, including if...
Reviewed and Approved by Steven Taormina, Certified Laboratories Regional Business Development Director – West, Cosmetic, OTC, and Supplements Amazon’s April 2024 updates to its dietary supplements selling policy include additional third-party verification...
Reviewed and Approved by Shelly Blackwell, Senior Director, Dietary Supplement and Tobacco, EAS Consulting Group 1-Minute Summary 21 CFR 111 requires written procedures for Quality Control (also know as Quality Unit – QU) operations in dietary supplement...
![How to Perform an Out of Specification Investigation for OTC Drug Products and Dietary Supplements [Step-by-Step]](https://certified-laboratories.com/wp-content/uploads/supplements-under-microscope.jpg)
