AdvaMed® Applauds Senate Cloture Vote to Advance CHIPS Act
“We are pleased to see the bipartisan Senate vote to advance the CHIPS Act today. The investments made in this bill will ensure the United States has a robust domestic…
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“We are pleased to see the bipartisan Senate vote to advance the CHIPS Act today. The investments made in this bill will ensure the United States has a robust domestic…
Mick Farrell, ResMed CEO and member of the AdvaMed® board of directors, joined AdvaMed®’s Scott Whitaker on the Medtech POV podcast to discuss how an agile company with skilled staff…
The Advanced Medical Technology Association® (AdvaMed®), the world’s largest trade association representing medical device manufacturers, took part in the Biden Administration’s 2022 Global Supply Chain Ministerial to discuss key strategies…
WASHINGTON, D.C. – This week, AdvaMed® President and CEO Scott Whitaker welcomed progress from President Joe Biden on the White House Cancer Moonshot, including appointing new members to the President’s Cancer Cabinet…
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This week, the Advanced Medical Technology Association® (AdvaMed®), the world’s largest trade association representing medical device manufacturers, sent a letter urging House Energy and Commerce and Senate Health, Education, Labor and…
Juliana Elstad, President and CEO of Vibrato Medical, recently joined AdvaMed®’s Scott Whitaker on The Medtech POV podcast for a conversation on several policy initiatives.
Deloitte released the findings of a follow-up survey of medical device manufacturers that found since the initial survey in July 2021 that semiconductor disruptions continue across multiple chip types and…
Renovia Inc., an AdvaMed® member and developer of non-surgical, treatments for female pelvic floor disorders, announced the U.S. Food and Drug Administration (FDA) has cleared its leva® Pelvic Health System…
Brought to you by AdvaMed®, Medtech POV with Scott Whitaker is a podcast that covers the intersection of medtech and policy from every perspective.
Senate committee passage of Medical Device User Fee Amendments legislation is an important step toward improving FDA review of medical technology to help patients.