Medical Device Studies: Regulatory Requirements and Adverse Event Reporting

Feb 25th, 2020Feb 26th, 2020
London, 17
GB
https://management-forum.co.uk/product/details/2269/medical-device-studies-regulatory-requirements-and-adverse-event-reporting?referrer=auntminnie
Phone:2077494730
An essential overview of medical device clinical evaluations, clinical investigations, postmarket clinical follow-up requirements, and adverse event and vigilance reporting.
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