CPR is recognised for delivering high quality research outcomes through the highest levels of customer service.

 CPR Pharma 2016

CPR provides each project with a dedicated Project Manager to ensure that milestones are reached, timelines are met and that our clients receive effective communication and ongoing status reports.

From the first conversation to the delivery of the final report, our clients are fully informed throughout the process; irrespective of project complexity. 

Our Project Managers and Monitors are involved in all aspects of clinical trial management, including:

  • Feasibility assessments

  • Study design

  • Protocol development & review

  • Development of patient information and consent forms

  • Ethics Committee submissions

  • Review of eCRFdesign and development

  • Investigator selection / facilitating investigator meetings

  • Site selection

  • Pre-study visits

  • Initiation visits

  • Monitoring

  • Close-out visits

  • CSR writing

  • Archiving

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