This is what ADAX can ensure for interventional trials:

  • Study feasibility and site selection
  • Collection and review of pre-study documents
  • Submissions to the Ethics Committees and Regulatory Authorities
  • Preparation, negotiation and execution of contracts with sites
  • Site Initiation, including training related to specific clinical trial
  • Good Clinical Practice (GCP) training for physicians and other research staff
  • Organization and execution of investigator meetings
  • Monitoring of clinical trials
  • Site management
  • Pharmacovigilance
  • Study Close-Out activities
  • Translations of study documents
  • Preparation of study files
  • Study materials management