Health Canada Guidance on Medical Device Recalls: Roles and Responsibilities
The new article clarifies the recall procedure in the context of the roles and responsibilities of the parties involved.
The new article clarifies the recall procedure in the context of the roles and responsibilities of the parties involved.
The new article describes in detail the recall process, highlighting the most important aspects associated with it.
The new article clarifies the reporting requirements associated with medical device recalls and explains the key terms and concepts used in this respect.
The article highlights the critical points of the regulatory approach concerning specific medical devices intended to be marketed and used in the Philippines.
The article provides an overview of the legal framework for labeling requirements applicable to medical devices intended to be marketed and used in Australia.