Clinical Trials

Whatever your Phase II-IV clinical development our team of dedicated scientific and medical professionals have the experience and expertise to help you move your compound forward.

GRC offers all aspects of monitoring and data management in all stages of clinical trials starting with study feasibility & protocol development to investigators’ selection & agreement, monitoring, data management, and ending with writing study reports & publication manuscript.

All our CRAs have medical qualification and are extensively trained on development process, ICH-GCP guidelines, Investigators’ responsibilities, Monitoring process, and Adverse events collection.


GRC provides client driven services through its experienced team of clinical research professionals by operating throughout the MENA region, utilizing the following fundamentals:

  • Pre-study Phase Activities
  • Site Initiation Visit
  • First-Patient In visit (FPI)
  • Investigator Database in different therapeutic areas
  • Site Database
  • Experienced Certified Clinical Resarch Coordinators (CCRCs)
  • Experienced Certified Clinical Research Associated (CCRAs)
  • Experienced Project Managers
  • Client driven services through IPRC’s experienced team of clinical research professionals
  • Operating regionally (MENA region coverage)
  • Comprehensive support for all phases of clinical trials
  • Follow up Monitoring Visits
  • Close-Out Visits