Published by
@ShahidNShah
@ShahidNShah
May 25 to May 27, 2021
It is an online event.
This intensive 3 – day course provides complete coverage of design control requirements for FDA Quality System Regulation, ANSI/AAMI/ISO 13485:2016, and the Medical Device Single Audit Program (MDSAP). With the participation of FDA representatives during the entire course, attendees have the unique opportunity to participate in a shared learning experience.
Continue reading at us-tdm-tso-15eb63ff4c6-1626e-169df4b0a12.force.com
May 26, 2021
It is an online event.
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