FDA’s mission

Section 1003(b) of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 393(b)) is amended— (1)in paragraph (2), by striking with respect to such products and inserting with respect to regulated products; (2)in paragraph (4), by striking (1) through (3) and inserting (1) through (4); (3)by redesignating paragraphs (2) through (4) as paragraphs (3) through (5); and (4)by inserting after paragraph (1) the following:

(2)establish a regulatory system that— (A)advances medical innovation by incorporating modern scientific tools, standards, and approaches to ensure the predictable, consistent, efficient, and reasonable review, clearance, approval, and licensing (as appropriate) of innovative products, including drugs, devices, and biological products; (B)protects the public health and enables patients to access novel products while promoting economic growth, innovation, competitiveness, and job creation among the industries regulated by this Act; (C)is based on the best available science; (D)allows for public participation and an open exchange of ideas; (E)promotes predictability, allows flexibility, and reduces uncertainty; (F)identifies and uses the most innovative and least burdensome tools for achieving regulatory ends; (G)ensures that regulations are accessible, consistent, transparent, written in plain language, and easy to understand; (H)measures, and seeks to improve, the actual results of regulatory requirements; and (I)incorporates a patient-focused benefit-risk framework that accounts for varying degrees of risk tolerance, including for people living with a life-impacting chronic disease or disability;