Modifications to 510(k) - Cleared devices: Assessing the impact of FDA's 2017 final guidance documents

On December 6, Danielle Humphrey and Kristin Zielinski Duggan led a complimentary webinar, which covered:

FDLI Introduction to Medical Device Law and Regulation

On November 7, 2018 Kristin M. Zielinski Duggan presented a session on organizational structures and medical device law and regulation at the Food and Drug Law Institute (FDLI) Introduction ...

The FDA Advisory Panel Meeting: Ensuring Success in an Unpredictable Process

How do you raise the likelihood of success of your FDA Medical Device Advisory Panel meeting?

Modifications to 510(k) Cleared Devices: Assessing the Impact of FDA's New Draft Guidance

Please join Hogan Lovells' Medical Device lawyers Danielle Humphrey and Kristin Zielinski Duggan for a complimentary webinar discussing the impact of FDA's new draft guidance documents on...

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