Medical & Scientific Writing

Our Medical and scientific Writing team is an integral part of clinical research. Our Medical Writers closely associate with biostatistics, medical affairs, safety and data management teams to deliver accurate, timely, and cost effective deliverables to the highest quality and scientific standards.

We have a wide breadth of experience drawn from the pharmaceutical industry and clinical research organizations.  All documents produced by us shall undergo thorough scientific, statistical, editorial and quality control review.

Our services include clinical and non-clinical writing, as well as scientific communications and medical writing consultancy.

Clinical and non clinical writing Scientific Communications:
  • Protocol synopsis for Phases I to IV studies
  • Study Protocols for Phases I to IV studies
  • Investigator Brochures
  • Study reference manuals
  • Informed consent documents (ICD)
  • Patient information sheet(PIS)
  • Clinical Study Reports (CSRs)
  • CER Writing
  • CSR Synopses for public disclosure
  • Clinical and non clinical sections of the  CTD
  • Summaries and overviews for EU and US
  • Patient Safety Narratives
  • Abstracts
  • Manuscripts
  • Marketing Materials
  • Medical Editing
  • Scientific Editing
  • Product and Package Labels
  • Presentations
  • Conference materials (abstracts, poster presentations and slide sets)
  • Journal/conference submission
  • Medical marketing reviews and reports
  • Literature reviews
  • Publications