Canada
The new article clarifies the reporting requirements associated with medical device recalls and explains the key terms and concepts used in this respect.
Canada
This article highlights the critical points related to the procedures to be followed by medical device manufacturers and other parties involved in case changes to medical devices allowed for marketing and use in Canada.
Canada
The new article describes specific types of changes to medical devices in detail and outlines the critical points related to the regulatory status thereof.
Canada
The article highlights the critical points related to the concept of significant changes in the context of medical devices allowed for marketing and use in Canada.
Canada
The article highlights the key points related to the regulatory status of in vitro diagnostic medical devices. Table of Contents Health Canada, the Canadian healthcare product regulatory authority, has released a draft guidance on determining medical device...
Canada
This article highlights he current regulations for medical devices in Canada, the process of registering compliant devices, potential changes being considered, and the potential impact on stakeholders. Table of Contents The use of medical devices is essential in...
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