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Pharmacovigilance – Medical Writing

Clinical development plan depends on the proper and errorless documentation. GAP offers a complete suite of medical writing function. Its administrations will back your clinical trial documentation needs from the early stages through post marketing and mature product development. Our writers are well versed in the writing manuscripts, medical marketing reviews and reports, journal/conference submission and educational material for patients, healthcare professionals and pharmaceutical industry personnel. We have shown qualities of our beneficial inputs in writing Standard Operating Procedures (SOPs) which deals with all aspects of drug development. Our expert writers ensure the clarity of scientific data and fully compliance according to the customer’s requirement.

    • Regulatory writing
    • Protocol and amendment writing
    • Investigator brochures development
    • CSR writing
    • Safety writing
    • Narrative writing
    • Article and review paper writing
    • White paper writing
    • Poster, abstract, publication writing
    • Promotional and educational material

Contact us for more information.