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  • Adverse Experience Reporting Requirements for Licensed Biological Products

    Federal Register · Uncategorized Document · Oct 27, 1994

    NCVIA created a new Title XXI of the Public Health Service Act (the PHS Act). … Periodic Reports Three comments on proposed Sec. 600.80(c)(2) noted a discrepancy on when the reporting period begins.

    Adverse Experience Reporting Requirements For Licensed BiologicalHealth and Human Services Department

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