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What s on the Agenda? Laboratory Developed Tests Added to the Unified Regulatory Agenda Signals FDA Movement Toward New Regulatory Framework | Epstein Becker & Green

What s on the Agenda? Laboratory Developed Tests Added to the Unified Regulatory Agenda Signals FDA Movement Toward New Regulatory Framework | Epstein Becker & Green
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What Does Revisited Chevron Deference Mean for Gov Agencies?

Keller and Heckman Attorneys analyze Chevron Deference standard Chevron v National Resources Defense Council and what it would mean to authority of regulatory agencies FDA EPA if it were reversed in coming SCOTUS ruling. Podcast.

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FDORA Passage Brings Significant Changes To FDA S Drug, Device, And Cosmetic Authorities | MoFo Life Sciences

The Consolidated Appropriations Act for 2023 was signed into law on December 29, 2022 and includes the Food and Drug Omnibus Reform Act (FDORA). FDORA authorizes a variety of new and.

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Congress Clarifies the Regulatory Classification of Contrast Agents, Radioactive Drugs, and OTC Monograph Drugs | Epstein Becker & Green

On December 29, 2022, President Biden signed into law H.R. 2617, the Consolidated Appropriations Act of 2023 (CAA23). Buried in this massive piece of legislation is Section 3621,.

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New FDA Reform Legislation: Congress Gifts a FDORA for the Holidays

On December 29, 2022, President Biden signed the Consolidated Appropriations Act, 2023 (H.R. 2617), an omnibus appropriations bill to fund the U.S…

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