As a company dedicated to comprehensive planning and organization of clinical trials, we offer preparing documentation that is essential to conduct clinical research trials. We offer flexible solutions, working with experienced medical writers in various therapeutic areas.

  • Clinical study protocol
  • Monitoring plan
  • Study operational manual
  • Case Report Form
  • Patient Information Sheet
  • Informed Consent Form
  • Other patient related documents: patient diary, patient emergency card, etc.
  • Investigator’s Brochure
  • IMPD
  • Final report