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Post Marketing Issues for Medical Devices: An Introduction

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Recorded April 8, 2020 | On-Demand Webinar

Review the definitions and purposes of complaint handling, Medical Device Reporting (MDR), recalls, corrections and removals, safety alerts, and ongoing monitoring/ postmarket surveillance. Examine risk communication initiatives.

This session was recorded as part of FDLI’s virtual Introduction to Medical Device Law and Regulation course in April 2020.

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