We aim to build within selected sites partners, the proper infrastructure for a functional CRU to conduct both academic and sponsored medical research. These Units handle the management of the ongoing clinical trials in the hospital, from feasibility till close out including:

   Selecting investigators according to therapeutic areas
   Liaising with IRBs
   Coordination between the different departments involved
        in the project
   Scheduling patient visits and appropriate tests per visit
   Handling biological samples designated for export
   Ensuring data collection and its integrity
   Designing IITs (Investigators Initiated Trials) with all related documentations and data analysis
   Wide range of site trainings

  Project Management

  Study Monitoring

  Medical Writing

  Medical Devices

  Regulatory Affairs

  Site Management

  Training and Development

  Data Management & Statistics

  Biological and IMP Logistics

  Quality Assurance