Precise Clinical Trial Documentation


It takes specific expertise, training and experience to create the documents that support your clinical trials. You will find it all at Clinipace. Our team of expert medical writers brings flexibility, competency and consistency to your Phase I–IV writing projects. Not only do we meet your deadlines, but we provide high-quality deliverables in a cost-effective approach.


  • CER reports
  • Management and writing of region-specific Module 1 documents
  • Scientific manuscripts
  • Support pharmacovigilance in the preparation of RMPs, DSURs,  PBRERs and annual safety reports
  • Writing for clinical trial applications
  • Writing of clinical study reports
  • Writing of IMPDs
  • Writing of Modules 2.5 and 2.7, Integrated Summaries of Efficacy and Safety, response documents
  • Writing of protocols and protocol amendments