Sec. 2. As used in this chapter, "biosimilar" refers to a biological product that: (1) has been licensed as a biosimilar product under 41 U.S.C. 262(k) or has been approved based on an application filed under 21 U.S.C. 355(b)(2); and (2) is highly similar to the reference product, with: (A) no clinically meaningful differences between the biological product and the reference product in terms of safety, purity, and potency of the product; and (B) only minor differences in clinically inactive components.
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