From the prescreening activities to the close out management : it’s not a matter of study focused plans as much as country and site focus from planning to developing executing and management . Our healthcare professionals are dedicated to:

   Site Selection
   Sites and Regulatory Authorities Submissions
   Agreements negotiation and follow up
   TMF management
   ICFs (Informed consent forms) creation and adaptation to the countries and sites
        requirements & other study materials (IB, patient diaries, patient clinic cards…)
   Study Initiation and Monitoring
   Investigators motivation
   Patient recruitment and retention
   Sites interaction from the set up, start up till the follow up
   Providers management and follow-up
   CRFs and DRFs management-
   Close out activities

  Project Management

  Study Monitoring

  Medical Devices

  Regulatory Affairs

  Site Management

  Training and Development

  Biological and IMP Logistics

  Quality Assurance

Our social responsibility commitment
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