Reviewed and Approved by Matt Traynor, PhD, Vice President, Innovation and Validation, Certified Laboratories 1-Minute Summary COAs provide key technical details that are often absent from the sample submission form. They help us choose the most...
Reviewed and Approved by Shelly Blackwell, Sr. Dir. Dietary Supplements & Tobacco Consulting, EAS Consulting Group 1-Minute Summary The FDA continues to cite failure to verify component specifications as a top observation during inspections. ...
Reviewed and Approved by Matt Traynor, PhD, Vice President, Innovation and Validation, Certified Laboratories 1-Minute Summary Measurement Uncertainty (MoU) explains why lab results are reported with a ± range — it’s a built-in measure of scientific...
Reviewed and Approved by Shelly Blackwell, Senior Director, Dietary Supplement and Tobacco, EAS Consulting Group 1-Minute Summary The FDA’s most common 21 CFR 111 compliance observations involve missing component and finished product specifications, as...
Reviewed and Approved by Shelly Blackwell, Senior Director, Dietary Supplements and Tobacco, EAS Consulting Group, a Certified Group company 1-Minute Summary Manufacturers should audit a contract lab’s personnel, test methods, equipment, and quality...
