Clinical Services


Phase I  (Bioequivalence/ Bioavailability/ Pharmacokinetics Studies)

IPRC has its own accredited clinical units, comprising of the following:

  • 2 clinics (30 beds each)
  • 2 emergency rooms
  • Accredited diagnostic lab
  • Dedicated temperature and humidity controlled pharmacy
  • Pool of more than 3,000 healthy volunteers

Phase II - IV (Clinical Trials)

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

  • Experienced certified clinical research coordinators (cCRCs)
  • Experienced certified clinical research associated (cCRAs)
  • Experienced project managers

Services

  • Feasibility studies
  • Project/ trial management
  • Site management
  • Regulatory submission and support
  • Study design
  • Protocol development
  • ICF & CRF development and translation
  • Investigators meetings
  • Clinical trials conduction
  • Study coordination
  • Study monitoring
  • Central IP storage and distribution services
  • Central laboratory services
  • Pharmacokinetics and statistical evaluation
  • Data management, medical writing and study eCTD report
  • Archiving of all study related data and (biological) materials