Phase I  (Bioequivalence/ Bioavailability/ Pharmacokinetics Studies)

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

• 6 clinics (30 beds each)
• 6 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 and CDISC
• Archiving of all study related data and (biological) materials