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FDA Guidance Provides Relief for MDR Reporting During a Pandemic

FDA Guidance Provides Relief for MDR Reporting During a Pandemic

Timely MDR reporting is a challenging regulatory requirement for the industry. A new FDA guidance provides much-needed relief during a pandemic.

Regulatory ComplianceNaveen AgarwalMarch 22, 2020FDA guidance, MDR, MDR reporting, pandemic, coronavirus crisus, coronavirus pandemic, adverse event reporting, COVID-19, FDA reporting requirements, MDR reporting update, FDA Medical Device Reporting GuidanceComment