Modifications to 510(k) - Cleared devices: Assessing the impact of FDA's 2017 final guidance documents
06 December 2018
On December 6, Danielle Humphrey and Kristin Zielinski Duggan led a complimentary webinar, which covered:
FDLI Introduction to Medical Device Law and Regulation
7-8 November 2018
On November 7, 2018 Danielle Humphrey presented a session titled "Clinical Investigations: Investigational Device Exemption (IDE), Institutional Review Boards (IRBs), and Informed Consent"...
9th Annual Advertising and Promotion of Medical Devices Conference
6-7 November 2018
On November 6, 2018, Danielle Humphrey presented a session on Medical Device Enforcement and Compliance at the AdvaMed Advertising and Promotion of Medical Devices Conference.
Master Class: Medical Device Clinical Research: The Path From Concept to Approval (Part 2)
21 October 2018 | 1:30 PM - 4:15 PM (PT)
Lina Kontos spoke in the Master Class: Medical Device Clinical Research: The Path From Concept to Approval (Part 2) session at the Magi's Clinical Research Conference - 2018 West on Sunday, ...
Mobile Medical Apps: Navigating the Legal Waters
Tuesday, 28 June, 1 p.m. EST
Monday, 11 July, 4 p.m. CET
Click here to register for the U.S.-focused session on 28 June at 1 p.m. EST.
Click here to register for the European-focused session on 11 July at 4 p.m. CET.
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