Be aware that Health Canada is actively testing “Performance Supplements” on the market. Implementation of a quality program in accordance with GMP is the only way to ensure product integrity and avoid enforcement actions. Read More >>
Between February and April of 2017, Health Canada inspectors visited 23 domestic Canadian Site Licence holders in order to assess their compliance with the Natural Health Product Good Manufacturing Practices. […] Read More >>
Sign Up for GMP Online Training Now! Companies that manufacture, package, label, or import dietary supplements or health products for sale in Canada and the U.S. must ensure that their […] Read More >>
Thursday, January 16, 2014 Three Part Webinar Series Provided by dicentra and Knowledge Bank Foods vs. Dietary Supplements: Cross Dressing Products Dear dicentra Subscriber, Jut in time for our upcoming […] Read More >>
The NHPD has recently released the finalized version of the “Quality of Natural Health Products Guide”, superceding the “Evidence for Quality of Finished Natural Health Products” after a 3 month […] Read More >>
DR. MOHAMMAD KHALID, PH.D., B.SC.(HONS) Dr. Khalid is the leading GMP expert at dicentra. He helps dicentra’s clients reach compliance with the FDA GMP Rule for Dietary Supplements (21 CFR […] Read More >>
March 26, 2013: dicentra conducted its first webinar of 2013. Critical American and Canadian updates including FDA’s proposed rules to amend cGMPs for food facilities under FSMA, the FDA’s Draft […] Read More >>
At the NBJ Summit this summer, Dr. Daniel Fabricant, Ph.D., director of the FDA’s Division of Dietary Supplement Programs, was asked his opinion on the status of the dietary […] Read More >>
Since the final good manufacturing practices (GMP) rule for dietary supplements was implemented in 2007, the Food and Drug Administration (FDA) has made it very clear that GMP inspections […] Read More >>
August 28, 2012 A Quick Note…. There have been a number of significant developments on the regulatory front for dietary supplements in the United States lately. For example, dietary supplement […] Read More >>
On July 24, 2012 the FDA issued a Warning letter to United Nutrition Labs for continually failing to comply with current Good Manufacturing Practices (cGMPs) after a thorough on-site […] Read More >>
By: William Morkel, BSc Director of Quality & Compliance It is standard practice amongst many countries to require an International Trade Certificate (ITC) to accompany any natural health product (NHP) […] Read More >>
By Heather VanBlarcom General Counsel & Senior Regulatory Specialist for Dietary Supplements On July 16, 2012, the U.S. Food & Drug Administration (FDA) filed an injunction against a New York […] Read More >>
By Manushvi Chadha, BPharm, RA Cert NHP, Cosmetic and Drug Regulatory Affairs Associate As of June 2012 the Natural Health Product Directorate (NHPD) has released a document outlining their new […] Read More >>
What is FDA Form 483? The FDA has started conducting inspections of establishments that manufacture, process, pack, or hold dietary supplements without prior notice to determine the establishment’s compliance with […] Read More >>
By Heather VanBlarcom General Counsel & Senior Regulatory Specialist for Dietary Supplements Over the weekend, the Chicago Tribune quoted Dr. Daniel Fabricant, head of the FDA’s Division of Dietary Supplement […] Read More >>
By Heather Van Blarcom General Counsel & Senior Regulatory Specialist – USA If your name is on the label of a dietary supplement product that you market and distribute, you […] Read More >>
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