Michael Kasser

Michael Kasser

Hogan Lovells

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New draft guidance on MR compatibility for medical devices

The U.S. Food and Drug Administration (FDA) has published a new draft guidance titled "Testing and Labeling Medical Devices for Safety in the Magnetic Resonance (MR) Environment." ...more

8/13/2019  /  Comment Period , Draft Guidance , Food and Drug Administration (FDA) , Life Sciences , Medical Devices , Regulatory Agenda , Regulatory Oversight , Rulemaking Process
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