FROM PROTOCOL AND CRF DEVELOPMENT TO FINAL REPORT

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  • Medical Writing: Protocol, CRF, other study-related documents and forms

    Compiling regulatory documents and getting regulatory approvals

    Management of the Clinical Part

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  • Clinical Monitoring

    Safety Assessment

    Data Management

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  • Bioassay

    Calculation of Pharmacokinetic Parameters

    Statistical Analysis and Reporting

    Final Report

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