Published Works | Barnett International | 30 January 2020

Medical Device Development: Regulation and Law 2020

Our Medical Device and Technology Regulatory team co-authored a comprehensive analysis of U.S. medical device and diagnostics development, premarket clearance/approval requirements, and postmarket compliance.

Medical Device Development: Regulation and Law, 2020 Edition offers analysis of new U.S. Food and Drug Administration device regulations, including all new significant guidance documents, and addresses how emerging developments and trends are reshaping medical device and combination product regulations in the United States.

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