The Division of Industry and Consumer Education (DICE) in the Center for Devices and Radiological Health (CDRH) will be hosting a workshop for medical device manufacturers on November 6, 2018. The workshop, which has a webinar format, will focus on 2 parts of the Quality Systems Regulation (21 CFR Part 820): Production and Process Controls and Documents; and Change Control, and Records. Each session is an hour with a presentation followed by a Q&A session. This looks like a good way to fit in some continuing education on Quality Systems for device manufacturing.

Text Copyright © 2018 Katrina Rogers