Enabling you to identify and mitigate the intrinsic risk in your operations, supply chains and business processes.
Evaluating how your products and services meet and exceed quality, safety, sustainability and performance standards.
Validating the specifications, value and safety of your raw materials, products and assets.
Recently, Health Canada announced that it will require manufacturers and importers to send Mandatory Problem Reports (MPRs) to its Health Canada Vigilance-Medical Device Program Reporting Program (CVMD) starting on October 3, 2011.
More specifically, this new requirement will affect those companies with medical device establishment licenses and Canadian Medical Devices Conformity Assessment System (CMDCAS) accreditations.
To learn more about this subject , please reach out to the Canada Vigilance program at firstname.lastname@example.org or 613.957.0337.