Regulatory, Compliance, and More.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
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