Reviewed and Approved by Matilda Baghdasarian, Laboratory Services Associate Director 1-Minute Summary Health Canada’s NHP GMPs Version 4.0 takes effect March 4, 2026, replacing the 2015 guide. Every natural health product (NHP) must now have a...
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...
