What we do

  • Managing and fulfilling staff requirements and recruitment.
  • Site Identification and Feasibility Services in order to identify the appropriated sites for each study
  • Design of clinical trials including preparation of the Protocol and the Patient Material (including ICF)
  • Document customisation (as per Local Regulatory / Ethics Requirements)
  • Document translation and translation review
  • Vendor Identification 
  • Budget Negotiation with Sites / Vendors and Clinical Agreement finalisation
  • Submission to Authorities for Clinical study approval
  • Monitoring Overview