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  • Content Creation and Management

    • Place of origin:  

      China

    system for drug substance and drug product; M4: Pharmacology, pharmocodynamic, pharmacokinetic, toxicology research reports, etc.; M5: Clinical study protocol, clinical study report, investigator brochure, ccds, package insert, etc. Documents from the medical device company: Patient Information Patient Reported Outcomes (PROs) Medical device safety and pharmacovigilance document Clinical trial pr

    [Related Keywords : medical terminology manag]

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