Sec. 3205. Public workshop on cell therapies

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Not later than 3 years after the date of the enactment of this Act, the Secretary, acting through the Commissioner of Food and Drugs, shall convene a public workshop with relevant stakeholders to discuss best practices on generating scientific data necessary to further facilitate the development of certain human cell-, tissue-, and cellular-based medical products (and the latest scientific information about such products) that are regulated as drugs under the Federal Food, Drug, and Cosmetic Act ( 21 U.S.C. 301 et seq. ) and biological products under section 351 of the Public Health Service Act ( 42 U.S.C. 262 ), namely, stem cell and other cellular therapies .

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Sec. 3205

Public workshop on cell therapies

U.S.C.§ 301

U.S.C.§ 262

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