Clinical trial support is on a personal basis and tailored to client requirements. Working hours are customised to suit individual project needs. We offer:

  • Study monitoring
  • Project management
  • Study site selection and setup
  • Ethics committee submissions
  • Hospital Trust / R & D approval and contract negotiation
  • CRF design
  • Organisation of Investigator Meetings
  • Clinical Study Report and SOP writing

We are also able to take on large monitoring contracts as we have an established network of colleagues and associates throughout the UK and Europe.

Please see examples of our previous experience.

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