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481. Investigational enzyme replacement therapy products: nonclinical assessment

482. Investigational in vitro diagnostics in oncology trials: streamlined submission process for study risk determination

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

484. 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

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

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

487. Adaptive designs for clinical trials of drugs and biologics

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

489. 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

490. VA health IT modernization: historical perspective on prior contracts and update on plans for new initiative : report to the House Committee on Oversight and Government Reform, Subcommittee on Information Technology