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31

May 2022

ALERT: New European Union In Vitro Diagnostics Regulations (EU IVDR) to replace In Vitro Diagnostic Medical Devices Directive (98/79/EC)
ALERT: New European Union In Vitro Diagnostics Regulations (EU IVDR) to replace In Vitro Diagnostic Medical Devices Directive (98/79/EC)
By
The new European Union In Vitro Diagnostics Regulations (EU IVDR) entered into application on May 26, 2022, to replace In Vitro Diagnostic Medical Devices Directive (98/79/EC). Manufacturers, authorized representatives, importers, and […] Read More >>

14

Apr 2022

How to Get a CE for a Medical Device
How to Get a CE for a Medical Device
By
Medical devices in the European Union (EU) are approved through a different mechanism than the approval process in the United States or Canada. The approval of medical devices intended for […] Read More >>
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 >>
Additional Residue Testing Requirements for Meat & Poultry Products Exported to the European Union
February 27, 2012 By
By Ryan Ramdeo, International Regulatory Affairs Associate February 27, 2012 As of February 17, 2012 USDA has announced revisions to the requirements for the export of meat products to the […] Read More >>
Successful EU response to BSE
February 5, 2012 By
By: Arwen Brooks – Quality Assurance and Regulatory Affairs Assistant February 6, 2012 BSE – a crisis in Europe and worldwide In the past two decades, Bovine Spongiform Encephalopathy (BSE) […] 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 >>

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