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Medical writing is an established core function at VST. Our medical writing team is fully integrated with the medical monitoring, pharmacovigilance, and biostatistics teams. The group skillfully handles writing projects related to drugs, biologics, and medical devices.

Our writers have experience with complex medical research topics such as proteomics, epidemiology, and pharmacogenomics. VST has established procedures for document management and a broad collective experience in current electronic submission formats and standards. Our documents undergo rigorous quality assurance review before delivery to our clients.

Medical Writing Projects include:

    • Clinical Study Protocols, Case Report Forms
    • Informed Consent Forms, Patient Information Sheets
    • Clinical Study Reports (Phase I – IV)
    • Narratives
    • Clinical Summaries, Clinical Overviews
    • Tabulated Summaries
    • Product Monographs
    • Benefit Risk Assessment Reports
    • Investigator Brochures and updates
    • Periodic Safety Update Reports (PSURs)
    • Integrated Summaries of Safety and Efficacy (ISS/ISEs)
    • Literature Reviews
    • Posters, Abstracts, and Manuscripts
    • Abstracts and Presentations
    • White Papers/Journal Articles
    • Quality Control Services