• Last updated：2024-08-13
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The CDE has launched “Pay-For-Service Consultation” to promote the development of the medical device industry. This service assists industry, academia, and research institutions in incorporating regulatory considerations and planning into the medical device development process early on. Our services cover three main categories: regulatory strategies for market approval, preclinical testing, and clinical investigations. We offer service plans designed to help medical device developers understand the pathways to market approval and ensure that their preclinical and clinical documentation meets regulatory requirements.