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August 9, 2022 1:00 pm Virtual
AUGUST 9, 1:00 PM MT
This webinar is designed to inform attendees about the FDA’s proposed rule to amend the device current good manufacturing practice (CGMP) requirements of the Quality System (QS) Regulation to align more closely with the international consensus standard for Quality Management Systems for medical devices used by many other regulatory authorities around the world.
If you’re a medical device professional involved in regulatory affairs, supply chain, design and manufacturing and quality, you won’t want to miss this discussion.
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