Consumer Medical Devices

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Submission

Letter regarding the Healthcare Distribution Alliance position on the Draft Guidance for Industry: Initiation of Voluntary Recalls.

Jun 25, 2019

Submission

Enclosed herein are comments on "510(k) Device Modifications: Deciding When to Submit a 510(k) for a Change to an Existing Device: Public Meeting: Request for Comments".

Jul 12, 2013

Submission

CHPA supports FDA's goals of reducing medical errors, simplifying device use information into data systems, identifying devices with adverse events, facilitating recall efficiency, and focusing communication.

Nov 7, 2012

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The foundation leads influential, innovative educational initiatives that address specific areas where consumers need guidance and support.

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CHPA is instrumental in shaping the policy and regulatory environment in the OTC medicine, dietary supplement, and consumer medical device industries.

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