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311. Compliance policy for limited modifications to certain marketed tobacco products

312. Adaptive designs for clinical trials of drugs and biologics

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

314. 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

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

316. 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

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

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