About Us

Pharmaceutical Research Organization works hand-in-hand with the study sponsor and their representatives, Institutional Review Boards, Investigative Sites, and patients to facilitate a smooth clinical trial process from onset to completion by:

  • Identifying Qualified and Experienced Investigative Sites
  • Protocol Review and Feasibility Analysis for Investigative Sites
  • Recruitment and Training of a Principal Investigator, and any Sub-Investigators
  • Recruitment and Training of Ancillary Clinical Staff as appropriate
  • Contract and Budget Negotiation
  • Regulatory Affairs Management
  • Research-Dedicated Study Coordinator
  • Placement and Training
  • Patient Recruitment and Screening
  • Qualified Patient Enrollment and Follow-Up
  • Data Collection
  • Internal Quality Control
  • GCP/ICH Annual Training for Principal Investigators
  • Continuing Education