Cispact offers a comprehensive range of medical writing services that includes goal setting, strategizing, creation and analysis of scientific well-structured clinical and regulatory documents. These services are provided throughout an entire product life-cycle for better understanding of a clinical program to patients, sponsors and regulatory bodies. Our team of specialised medical writers, editors and peer reviewers, who come from medical and life sciences backgrounds work closely with clients to understand their requirements. We are committed to provide accurate, timely, high-quality deliverables to meet all publishing and reporting needs including protocols, CSRs and regulatory practices.


  • Safety Data Migration, Archiving and IT Recovery Systems

  • Quality and Compliance Check
  • Global Safety Database Creation & Validation
  • SOP Development
  • Regulatory Audit & Compliance Support
  • Setting up of end to end PV System
  • EU and local QPPV Services


  • Support in creation of presentations for medical conferences and agency meets

  • Support in creation of collaterals, posters, leaflets, flyers for professional meetings

  • Support in preparation of white papers, publications, and manuscripts

  • Help in reviewing medical literature and researches

 Our team of professional writers extensively expertise in creating highly regulated documents to aid drugs, trials, and devices worldwide.