TGA Guidance on Uniform Recall Procedure for Therapeutic Goods: Overview
The article describes the recall procedures to ensure the continued safety of medical devices and other therapeutic products allowed for marketing and use in Australia.
The article describes the recall procedures to ensure the continued safety of medical devices and other therapeutic products allowed for marketing and use in Australia.
The new article describes in detail the first three steps of a recall process, which include obtaining information and distribution status, conducting a risk analysis, and deciding on the type, class, and level of recall.
The article highlights the critical points related to the recall procedures applicable to medical devices allowed for marketing and use in Canada.
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.
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