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Medical Device Manufacturer Requirements: An Introduction to Registration and Listing of Establishments

A session from FDLI's Introduction to Medical Device Law and Regulation
Recorded November 16-18, 2021

Medical Device Manufacturer Requirements: An Introduction to Registration and Listing of Establishments

Define registration and listing and their applications to the medical device industry. Assess who does and who does not have to register and list and how the process works.

Abeba Habtemariam, Counsel, Arnold & Porter LLP

This session was recorded as part of FDLI’s Virtual Introduction to Medical Device Law and Regulation Course in November 2022.

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Kiana Walker2024-07-19T11:57:10-04:00