Supervision of clinical trial of medical device in China is stricter and stricter. With the latest medical device regulation coming into practice, more concrete clinical trial methods of medical device and its related regulations will be promulgated. Interpretation and practice of Clinical Trial Regulation of Medical Device Seminar held by the Guangdong Medical Device Quality Surveillance and Test Institute, China Quality Association for Pharmaceuticals (CQAP) and Osmunda Medical Device Consulting Organization will open on December 18th to embed the regulation requirement of clinical trial into medical device enterprises in domestic and abroad and to explore the prospect of clinical trial regulation of medical device.
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