Q CRC is a consultancy providing services to the life science sector within design, planning and management of clinical trials and clinical drug development plans.

Design and project management of Clinical Trials and Clinical Development Plans

  • Trial and development plan design in close collaboration with experts and customer
  • Protocol synopsis
  • Full protocol
  • Trial initiation including; site selection, regulatory and ethics approvals, trial supply logistics
  • Trial and development plan management
  • Development of trial specific documents; development plans, monitoring plans, clinical trial report etc.
  • Vendor management and outsourcing; preparing requests for proposals, selecting and management of CROs,


    • Phase 1 to phase 4 trials
    • Project management from phase 1 to phase 3
    • Therapeutic areas; vaccines, dermatology, immunology

When necessary, Q CRC work in close collaborations with external partners under subcontracts.