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331. Adaptive designs for clinical trials of drugs and biologics

332. Considerations for the development of dried plasma products intended for transfusion

333. Food labeling: serving sizes of foods that can reasonably be consumed at one eating occasion, reference amounts customarily consumed, serving size-related issues, dual-column labeling, and miscellaneous topics

334. Enforcement priorities for electronic nicotine delivery systems (ENDS) and other deemed products on the market without premarket authorization

335. Food safety: federal efforts to manage the risk of arsenic in rice : report to the Ranking Member, Subcommittee on Labor, Health and Human Services, Education, and Related Agencies, Committee on Appropriations, House of Representatives

337. Keeping America's food safe: a blueprint for fixing the food safety system at the U.S. Department of Health and Human Services

338. One percent of drugs with Medicaid reimbursement were not FDA-approved

339. Most hospitals obtain compounded drugs from outsourcing facilities, which must meet FDA quality standards