Published by
@ShahidNShah
@ShahidNShah
November 15 to November 19, 2021
It is an online event.
Upon completing this program, participants will take home the knowledge to examine their quality management system to determine if it complies with both FDA Quality System requirements and 13485 requirements and recognize where improvements are needed. Participants will learn about the FDA inspectional approach and the Medical Device Single Audit Program. This course will empower the attendee with the knowledge to successfully host an FDA/MDSAP audit.
Continue reading at us-tdm-tso-15eb63ff4c6-1626e-169df4b0a12.force.com
November 15 to November 16, 2021
Jeddah, Saudi Arabia
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