Medical writing

Our medical writing services are based on our extensive experience in the pharmaceutical industry and our commitment to quality, which ensures clear, concise and well-structured documents.

Global Clinical Research has a team of experienced medical writers with medical and scientific expertise to provide high-quality clinical study documents compliant with ICH-GCP guidelines and regulatory requirements.

From protocol writing to the final study report preparation, our medical writers collaborate with bio-statisticians and project team members to produce comprehensive, submission-ready documents for all stages of clinical development.

All documents are peer-reviewed to ensure medical and scientific accuracy and are subjected to continuous quality control to guarantee compliance ensuring high-quality deliverable, on-time. We provide medical writing services as part of the comprehensive clinical trial program or as a stand-alone service.

Our medical writers help you in the preparation of the following:

  • Clinical study protocols
  • Informed consent forms
  • Clinical study reports – Phase I to IV
  • Clinical overview and Clinical Summary
  • Quality Compliance Dossier Preparation
  • DSMB and Pharmacy manuals
  • SOP dossier for clinical and Laboratory Procedures
  • Grant Writing
  • Data Analysis
  • Manuscripts Preparation and Submission

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