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Medical Writing

Pharmazz with its experienced and efficient team, provides a complete solution for your medical writing requirements both, during the clinical phase as well as marketing phase. Our medical writers provide solutions for your regulatory submissions and publications to add value to your research work. A team of project managers, biostatisticians and data managers also works in cohesion with our medical writers to provide insights into the clinical trials and effectively communicate your research reports with the regulatory bodies and publications.

Overview – Medical Writing

  • Reports submitted in USFDA, EMEA and DCGI
  • Full time experienced team of medical writers holding a scientific degree, usually a master’s or PhD from reputed organizations; have an experience in scientific and/or clinical research
  • Our medical writing team works closely with leading physicians across the country

Services:

Regulatory

  • Protocols
  • Investigators Brochure
  • Clinical Study Report
  • Patient Documents like Informed Consent Forms

Commercial

  • Review Articles
  • Manuscripts
  • Case Studies
  • Conference Abstracts