• Development of the scientific project of a clinical trial and/or a study of outcome
  • Writing of the study protocol
  • Design, plan, and implementation of the Electronic Case Report Form (eCRF)
  • Drafting of the Clinical Study Report (ICH-E3 Standard)
  • Ethical/Administrative Approvals*
  • Clinical trial monitoring *
  • Project management *
  • Pharmacovigilance *
  • Data Management *
  • Statistical analyses *
  • Centralized Laboratory *
  • Experimental drug trials setup *

* Activities carried out by Compass in partnership with CROs and companies specialized in the field.