Certificate in Medical Device Registration Processes
-- ViewingNowThe Certificate in Medical Device Regulation Processes is a comprehensive course designed to provide learners with critical insights into the complex world of medical device registration. This course highlights the importance of regulatory compliance, ensuring product safety, and improving patient outcomes.
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⢠Introduction to Medical Device Registration
⢠Understanding Medical Device Classification
⢠Global Medical Device Regulations Overview
⢠Medical Device Registration Process in the US (FDA)
⢠European Medical Device Regulation (MDR) and Registration
⢠Medical Device Registration in Canada (Health Canada)
⢠Medical Device Registration in Japan (MHLW)
⢠Medical Device Registration in Australia (TGA)
⢠Quality Management System (QMS) Requirements for Registration
⢠Post-Market Surveillance and Vigilance in Medical Device Registration
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