Regulatory Requirements for Medical Device Manufacturing and Quality System Regulation: An Introduction
Explore the background, purpose and regulatory requirements of the Quality System Regulation. Become familiar with the regulatory requirements for device manufacturing and distribution. Differentiate between International Standards Organization (ISO) and QSR requirements.
Allison Fulton, Partner, Sheppard Mullin Richter & Hampton LLP
This session was recorded as part of FDLI’s Virtual Introduction to Medical Device Law and Regulation Course in April 2020.
- +$100 for nonmembers
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