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Coverage & Payment / Diagnostics / Global & Trade / Government & Legislative Affairs / Health Equity / Legal / Regulatory Affairs / Small Business

AdvaMed’s Medical Innovation Agenda for the 118th Congress

AdvaMed’s medtech priorities for the 118th Congress highlight opportunities to address the most important issues facing patients and the medical technology industry today.

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Automatic External Defibrillators (AEDs)

A lack of public information persists about sterilizing medical devices with ethylene oxide gas. That’s why Scott Whitaker talked with Dr. Lucy Fraiser, a board-certified toxicologist, about the facts.

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Health Equity

Women and Heart Disease

Heart attack symptoms in women can be different than in men and less well-known as heart attack-related. Women need their heart disease recognized and treated on equal footing with men.

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.

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Ethylene Oxide / Government & Legislative Affairs

Medical Device Sterilization and Public Health

A lack of public information persists about sterilizing medical devices with ethylene oxide gas. That’s why Scott Whitaker talked with Dr. Lucy Fraiser, a board-certified toxicologist, about the facts.

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Coverage & Payment / Global & Trade / Government & Legislative Affairs / Health Equity / Investor Relations / Regulatory Affairs / Small Business

AdvaMed’s Top 10 Medtech Wins in 2022

From MDUFA V and the major investments in semiconductor chip manufacturing in the CHIPS Act, to addressing global supply chain issues and supporting our AdvaMed Accel companies, 2022 was a…

Press Contacts

If you have media inquiries, please contact:

Cody Uhing, Director, Communications & Media Relations, 202-316-1423

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Government & Legislative Affairs / Regulatory Affairs

MDUFA V Enacted, Ushering in Next Era of Medtech for Patients

Congress overwhelmingly approved the fifth Medical Device User Fee Amendment (MDUFA) agreement, helping to ensure new medical technology receives a more efficient FDA review to reach patients sooner if approved.

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