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8491. Prescription Drug User Fee Act waivers, reductions, and refunds for drug and biological products

8492. Process to request a review of FDA's decision not to issue certain export certificates for devices: guidance for industry and Food and Drug Administration staff

8493. Smallpox (variola virus) infection: developing drugs for treatment or prevention

8494. Compliance policy for limited modifications to certain marketed tobacco products

8495. Adaptive designs for clinical trials of drugs and biologics

8496. Considerations for the development of dried plasma products intended for transfusion

8497. 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

8498. Enforcement priorities for electronic nicotine delivery systems (ENDS) and other deemed products on the market without premarket authorization