Adapted full training program according to international standards ICH and 21 CFR, in addition to local regulatory requirements in the field of Clinical research (Medical writing requirements, Regulatory guidelines, SAE and Pharmacovigilance) for Clinical research professionals like:

   Clinical Research Coordinators
   Clinical Research Associates
   Clinical Project Managers
   IRB members
   Data entry clerks
   Clinical research Pharmacists
   Clinical research laboratory technician

  Project Management

  Study Monitoring

  Medical Devices

  Regulatory Affairs

  Site Management

  Training and Development

  Biological and IMP Logistics

  Quality Assurance

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