Webinar On FDA Guidance: Design Considerations for Pivotal Clinical Investigations for Medical Devices

fda cfr 21 part 11, medical device consultants, medical device manufacturers, medical device industries, medical device 510 k, 510 k submission, fda 510 k requirements, medical device products, fda requirements for medical device manufacturers

14 April 2014 from 1pm to 2:30pm

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