Services

Clinical Trials (Phase I-IV)

Overview

PRU offers comprehensive clinical trial services for pharmaceutical companies, from early-phase studies to post-marketing surveillance. Our experienced team manages all aspects of clinical research ensuring compliance with GCP, FDA, and ICH guidelines.

KeyBenefits

  • Dedicated clinical trial unit with 40+ beds
  • 24/7 medical supervision and emergency care
  • Experienced principal investigators and study coordinators
  • Access to diverse patient populations
  • Electronic data capture and monitoring systems
  • Regulatory expertise for MENA region submissions

Methodology

  1. 1
    Protocol design and ethics committee approval
  2. 2
    Site preparation and investigator training
  3. 3
    Patient recruitment and informed consent
  4. 4
    Study conduct with real-time monitoring
  5. 5
    Safety monitoring and adverse event reporting
  6. 6
    Data management, analysis, and final reporting