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Regulatory Barriers to Trade for Consumer Health Products
May 28, 2012 By
By Dr. John Harrison, PhD, MSc, BSc Senior Government Relations Advisor So you want to import a consumer health product from the U.S.A. to Canada. Good luck! There are many […] Read More >>
The Industry Effect on Food Regulations
February 13, 2012 By
By: Rupika Malhotra, MSc – Food, Scientific and Regulatory Affairs Associate February 13, 2012 With the introduction of any new set of guidelines, regulations or changes impacting any sector of […] Read More >>
FDA Targets Tainted Dietary Supplements
December 20, 2011 By
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 >>
Clinical Update on Resveratrol
December 5, 2011 By
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 >>
Health Canada Releases Policy Statement on Nanomaterials
November 14, 2011 By
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 >>
Food Taxation: Will Health Canada adopt European Trends to Tax Unhealthy Foods?
October 17, 2011 By
Rupika Malhotra, MSc Scientific and Regulatory Affairs Associate, Dicentra With recent developments and proposed changes to energy drink regulations in Canada, questions on taxation of health harming foods have come […] Read More >>
FDA Participates in Global Efforts to Protect Consumers and Patients from Unsafe Drugs on the Internet
October 3, 2011 By
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 >>
Resveratrol: Potent Antioxidant by Day, Acne Treatment by Night
September 26, 2011 By
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 >>
NHPD Seeks Industry Feedback on A New Risk Based Approach to Site Licensing
September 19, 2011 By
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 >>
FDA Updates – Dealing with Natural Products in a Global Market
September 12, 2011 By
Manushvi Chadha, BPharm, RA Cert Regulatory Associate, Dicentra The FDA recognizes that the production of FDA-regulated products has gone international, with more globalization on the way. Not only wholly manufactured […] Read More >>
Non-Medicinal Ingredient Labeling for Nonprescription Drug Products
August 8, 2011 By
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 >>

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