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Killing Americans by Stifling Medical Innovation: The Medical Device "Safety" Act of 2009

The misnamed Medical Device Safety Act of 2009 would gut the carefully crafted regulation of medical devices by the Food and Drug Administration, exposing developers to the conflicting laws and regulations of 50 different states and subjecting them to abusive and punitive tort litigation.
New York United States United Kingdom West Virginia Justice Scalia Michael Kinsley

US Regulatory Considerations Applicable to Digital Health Providers and Suppliers - Part III: FDCA | K&L Gates LLP

This article examines another major regulatory regime relevant to mHealth application developers – the Federal Food, Drug and Cosmetic Act (FDCA), as well as regulatory issues unique to...
United States Enforcement Policy For Digital Health Devices Commission Act Kl Gates Regulatory Issues Unique To Companies Us Food Drug Administration

Digital Health Providers and Suppliers US Regulatory Considerations

This article examines another major regulatory regime relevant to mHealth application developers – the Federal Food, Drug and Cosmetic Act FDCA, as well as regulatory issues unique to non-US companies.
United States Enforcement Policy For Digital Health Devices Commission Act Regulatory Issues Unique To Companies Us Food Drug Administration Device Software Functions

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