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

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

503. 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

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

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

506. Adaptive designs for clinical trials of drugs and biologics

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

508. 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

509. 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

510. Coast Guard health records: timely acquisition of new system is critical to overcoming challenges with paper process : testimony before the Subcommittee on Coast Guard and Maritime Transportation, Committee on Transportation and Infrastructure, House of Representatives