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Low Risk Veterinary Health Product Interim Notification Program undergoes software upgrade and clarifies role of “Canadian Representative”
July 3, 2014 By
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 >>
dicentra Welcomes Our Newest Team Member
May 8, 2013 By
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 >>

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Apr 2013

GMP Compliance: The Benefits of Implementation
April 1, 2013 By
GMPs are a set of industry best practices to help ensure the safety, quality and efficacy of a natural health product. Natural health products (NHPs) are a valuable tool in […] Read More >>
dicentra’s Regulatory Webinar – Q1: March 26, 2013
March 26, 2013 By
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 >>
Supplier Qualification – Is your Supplier Qualified?
March 18, 2013 By
Supplier qualification is a requirement of the regulations, as set out by 21 CFR part 111.75. Setting up a proper supplier qualification program is an essential step in maintaining dietary […] Read More >>
Recent Enforcement Actions Highlight Need for Proper Auditing of Contract Laboratories
January 22, 2013 By
By: William Morkel, BSc Director of Quality & Compliance Recent closure of a testing laboratory in Mississauga, Ontario by Health Canada illustrates the need for companies to audit third party/contract […] Read More >>
GMP Procedures: Considerations for Manufacturers
September 4, 2012 By
  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 >>
Quarterly Newsletter – Q3 – 2012
August 28, 2012 By
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 >>
If You Think the FDA’s cGMPs Don’t Apply to You, Think Again!
April 30, 2012 By
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 >>
Dicentra Newsletter – Issue #9
June 9, 2010 By
The Sale of Unlicensed Natural Health Products, Exemption Numbers, and You! Natural Health Products (Unprocessed Product Licence Applications) Regulations The regulatory solution many have been waiting for may be on […] Read More >>

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