An Overview of Medical Device Classes in Canada
By: By: Ivy Tang, PRINCIPAL REGULATORY CONSULTANT, email Introduction In Canada, the intended use of a medical device primarily determines its class. Classification must be consistent with [...]
Medical Devices Canada | Regulatory Overview
By: By: Ivy Tang, PRINCIPAL REGULATORY CONSULTANT, email Introduction to Medical Devices in Canada Medical devices are defined in the Food and Drugs Act as health or medical instruments used for [...]
Medtech Canada 2024 and Dell Tech’s Medical Device Regulatory & Quality Services
By: Steve McCarthy, DIRECTOR OF REGULATORY AFFAIRS, email Dell Tech attended the Medtech Canada 2024 Regulatory & Quality conference in Ottawa at the end of April. This hybrid event marked [...]
Health Canada Reclassifies Disinfectants
High-Level Disinfectants Reclassified…Be in the know. By: Sarah Calder, Regulatory Affairs Specialist, email Last month Health Canada released a notice of the reclassification of high-level [...]
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