FDA Medical Device Free Training

Practical Guide to FDA Medical Device Submissions: 510(k), PMA and Exemption Pathways (WEBINAR)

Dublin, April 15, 2026 (GLOBE NEWSWIRE)-- The "Practical Guide to FDA Medical Device Submissions - 510(k), PMA and Exemption Pathways (Apr 14, 2026)" training has been added to ...

RAPS

FDA: All Device Review Staff Have Completed 'Least Burdensome' Training

In a report to Congress dated last week, the US Food and Drug Administration (FDA) says that all of its staff involved with premarket device reviews and their supervisors have undergone mandatory ...

JD Supra

FDA Proposes Premarket Framework for Robotically Assisted Surgical Devices

Drug & Device Team examines the Food and Drug Administration’s (FDA) draft guidance establishing a comprehensive premarket framework ...

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Practical Guide to FDA Medical Device Submissions: 510(k), PMA and Exemption Pathways (WEBINAR)

FDA: All Device Review Staff Have Completed 'Least Burdensome' Training

FDA Proposes Premarket Framework for Robotically Assisted Surgical Devices

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