Company operates according to current Good Manufacturing Practices under 21 CFR part 111 and part 117, with an FDA-compliant fulfillment facility in Reno, NV.
According to product recall reports, just a portion of products containing illegal ingredients were recalled following the issuance of warning letters.
With their resources, the AMA and FDA could have created something impactful on public health. Instead they opted to push out a smear job masquerading as CME.
With fewer recalls than conventional foods, drugs, animal products and medical devices, supplements could be considered the safest class of goods FDA regulates.
By Michael McGuffin, President, American Herbal Products Association (AHPA)06.02.22
Industry should view both proposed legislation and arguments against it with a critical eye, but let’s address legitimate concerns while dismissing strawmen.
Online ExclusivesBy Steve Mister, President & CEO, Council for Responsible Nutrition04.26.22
Sen. Dick Durbin (D-IL) and Sen. Mike Braun (R-IN) introduced a bill that would require dietary supplement manufacturers to file product information with FDA.
Technology that can track a sequence of transactions helps build trust among stakeholders along the supply chain, as well as between consumers and brands.
By Robert Galaza, CEO, TruTrace Technologies04.14.22
The U.S. Food and Drug Administration is prioritizing multiple ways to regulate the dietary supplements industry in its request for an $8.4 billion budget.
The independent safety review of seven probiotic strains demonstrates to consumers that the probiotics were vetted through studies and expert panel consensus.