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 >>
The North American Compendium (NAC) has upgraded the software running the Interim Notification Pilot (INP) Program for Low Risk Veterinary Health Products (LRVHP), affecting certain aspects of the notification process. […] 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 >>
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 >>
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