Resource Library - Page 22 of 35 - AdvaMed®

Regulatory Affairs

AdvaMed® Letter to FDA: Letter to Owen Faris RE Clinical Trials Flex Proposals

Global & Trade

Medtech Europe Press Release: “Medtech Europe calls for a pause on IVDR and MDR implementation to facilitate the fight against COVID-19 and to safeguard Healthcare Systems”

Global & Trade

Medtech Europe: “Mitigating the Impact of COVID-19 on Healthcare Systems – Urgent Need to Pause the new Medical Technology Regulations Implementation”

Government & Legislative Affairs

Reed Smith: Summary of Selected Provisions of the Defense Production Act

masked lab technician looks into microscope

Diagnostics / VALID Act

AdvaMedDx® VALID Act Webinar, March 20, 2020 – Presentation

On March 5, 2020, the VALID Act was introduced in the Senate and House.

Listen to AdvaMed®'s Podcast

Brought to you by AdvaMed®, Medtech POV with Scott Whitaker is a podcast that covers the intersection of medtech and policy from every perspective.

Government & Legislative Affairs

Reed Smith: Defense Production Act – A webinar discussing the basics of the Defense Production Act and its application to the medical technology industry

Recommended language for states to use as a supplement to DHS CISA

“Dear Governor” Letter from 8 national health care products trade groups

Government & Legislative Affairs

Reed Smith: Executive Summary of the Defense Production Act

Previous
1
…
21
22
23
…
35
Next

Become a member to continue reading. Join AdvaMed®

Sign in to access AdvaMed® member-only content.