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PM CLTP BP M stands for Post Market Clinical Follow-up Plan.
Manufacturers of medical devices are required to file PM CLTP BP M.
PM CLTP BP M can be filled out by providing detailed information about the post-market clinical follow-up plan for a medical device.
The purpose of PM CLTP BP M is to ensure the safety and effectiveness of medical devices through the implementation of post-market clinical follow-up plans.
Information such as study design, objectives, endpoints, patient population, follow-up procedures, and data analysis must be reported on PM CLTP BP M.
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