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


► 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