Safety Monitoring in Phase 1 Clinical Trials

Medical Writing


We assign a medical writer who is responsible for managing the writing process. A communication plan is drawn up to ensure you are aware of progress against timelines.

Convex combine medicine, science, and technical writing to deliver documents for all stages of a clinical study project.

Our Medical Writing Services


Phase 1 Clinical Trials Endpoints

Clinical Study Documentation
  • Clinical Study Protocols and Amendments
  • Clinical study reports
  • Inform consent form
  • Patient Narratives
Regulatory Documentation
  • Investigator’s brochures
  • Investigational new drug documents
  • Common technical document (CTD/eCTD)
  • Technical documentation
Phase1 Clinical Trials

Safety Monitoring in Phase 1 Clinical Trials

Scientific Publications
  • Abstracts and manuscripts
  • Conference presentations
  • Research papers
  • Scientific posters

For more information about our medical writing services, please contact us at: info@convex.bg