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We believe this is appropriate because Section 351(i)(2) of the Public Health Service Act defines the terms biosimilar and biosimilarity to mean that a biosimilar is highly similar to its reference product, notwithstanding minor differences in clinically inactive components, and that there are no clinically meaningful differences between the biosimilar and the reference product in terms of the safety, purity, and potency of the product

Brett Thombs, Donna Reynolds, Eddy Lang, Stphane Groulx, and Brenda Wilson drafted the recommendations

Figure 1 shows the data selection carried out to achieve the final study sample

During the years of his darkest isolation and rancor, he spent several afternoons a week at either the El Sereno Branch Library or the Los Angeles Central Librarythat is, when he wasnt at the race track or at his stockbrokers