dicentra is proud to announce the launch of GMP Online Training for Natural Health Products beginning November 2011. For years, dicentra has been delivering on-site and off-site GMP training programs, […] Read More >>
By Arwen Brooks Quality Assurance and Regulatory Affairs Assistant, dicentra Dec. 15, 2010 — The FDA today announced new steps to target harmful products marketed as dietary supplements, including the […] Read More >>
Then he slid down the chimney. A rather tight pinch, but if Santa could do it, then so could the Grinch. He thought to himself, I must address this […] Read More >>
John Holtmann was born on May 24th, 1950, the youngest of Heinrich and Johanna Holtmann’s eight children. He grew up on a dairy farm in Rosser, Manitoba, and would want […] Read More >>
By: Ashleigh Hampton, MSc December 5, 2011 Previous reports of resveratrol have suggested that resveratrol undergoes extensive metabolism, thus resulting in a low bioavailability of the parent compound (As reviewed […] Read More >>
Clara di Tella, BSc, Pharm. QA Regulatory Affairs Specialist, dicentra Inc. On November 24, 2011 the European Food Safety Authority (EFSA), the Food and Agriculture Organization of the United Nations […] Read More >>
dicentra is pleased to announce our upcoming free Regulatory Update Webinar on Tuesday, December 6th at 1:00 pm ET. This is our fourth webinar of 2011 and you won’t want […] Read More >>
William Morkel, BSc Senior Quality Assurance and Regulatory Affairs Specialist, dicentra Inc. Under the current guidelines for Good Manufacturing Practices (GMPs) for Natural Health Products (NHPs), manufacturers and importers of […] Read More >>
Manushvi Chadha, BPharm, RA Cert Regulatory Affairs Associate, dicentra Inc. Nanomaterials are engineered molecules whose defining characteristic is their size – they range from 1-100 nanometers where each nano is […] Read More >>
FOR IMMEDIATE RELEASE Health Canada Announces Proposed New Approach to Regulating Caffeinated Energy Drinks Toronto, Canada, October 11, 2011 – On October 6, Canadian Health Minister Leona Aglukkaq announced a […] Read More >>
Clara di Tella, BSc, Pharm QA Regulatory Affairs Specialist, Dicentra The United States Food and Drug Administration along with regulatory agencies from 80 other countries have completed the International Internet […] Read More >>
Ashleigh Hampton, MSc Scientific and Regulatory Affairs Associate, Dicentra There have been some challenges faced while assessing the therapeutic effects of resveratrol in humans. Phase 1 clinical trials have reported […] Read More >>
William Morkel, BSc Senior Quality Assurance and Regulatory Affairs Specialist, Dicentra From late September to mid October the NHPD will be holding information sessions in Montreal, Toronto, Vancouver, and Halifax […] Read More >>
Novel Food Approval: EU Approves Rooster Comb Extract (RCE) Rupika Malhotra, MSc Regulatory Associate, Dicentra In recent years, several novel and arguably eccentric food ingredients have made their way into […] Read More >>
Health Canada Update: Non-Medicinal Ingredient Labeling for Nonprescription Drug Products Clara di Tella, BSc, Pharm QA Regulatory Affairs Specialist Health Canada has released a notice to inform drug manufacturers/sponsors of […] Read More >>
The follPrepared by Candice Cryne, M.Sc., Scientific Regulatory Associate, Dicentra Inc. What is Kava? Kava is the South Pacific herb Piper methysticum G. Forster, and the parts most commonly […] Read More >>
On December 22, 2010 the Natural Health Products Industry was informed by the NHPD that the compliance promotion transition period which was slated to end on March 1, 2011 is […] Read More >>
We are pleased to inform you that on Friday August 27, 2010, the documents entitled “Natural Health Products (NHP) Compliance and Enforcement Policy” (POL-0044), “Annex to the NHP Compliance and […] Read More >>
Dear stakeholders, As of August 9, 2010, NHPD will no longer accept Product Licence Applications (PLA) containing medicinal or non-medicinal ingredients which are not listed as acceptable ingredients in the […] Read More >>
Dear stakeholders, The Application Management Policy outlines the way in which Product Licence Applications for natural health products are submitted in accordance with the Natural Health Products Regulations. The […] Read More >>
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