Applying FDA's Rules in the New World of Online Marketing and Crowdsourcing

The 2019 Regulatory Affairs Professionals Society (RAPS) Regulatory Convergence will take place in Philadelphia.

Webinar: Understanding the FDA – Accelerating the Pathway to Approval for Point-of-Care Technologies

Senior director Susan D. Tiedy-Stevenson was a featured speaker for the webinar titled "Understanding the FDA – Accelerating the Pathway to Approval for Point-of-Care Technologies"...

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 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

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)

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

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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