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Clinical Research

With strong national and international Project Management and a network of researchers and scientists in 17 major cities of the country, Farzan Clinical Research is the pioneer of clinical research in Iran. We know local laws and cultural aspects which have to be considered during a clinical research. Timeliness and responsiveness are the most important elements when sponsors choose our CRO. Our Clinical Research Division provides comprehensive services for managing Phase II-IV clinical studies conducted at multiple centers around the country.

 

Site Initiation

  • Research Site and Investigator Selection
  • Investigators’ Meetings
  • Personnel Training
  • Site Initiation
  • Site Set-up


Site Monitoring

  • Complete Monitoring Activities Associated with Phase II-IV of Clinical Research
  • Source Document Review and Data Verification
  • Checking Internal Consistency of CRF Data
  • Data Query Management
  • Issuing Data Alerts to CDM
  • Monitoring of Enrollment Rate and Patient Eligibility Criteria
  • Training
  • Site Closure


Project Management

  • Study Coordination
  • Budget and Time Management
  • CRAs and Project Team
  • Progress Reports
  • Medical Monitoring and Reporting of SAEs


Quality Assurance

Farzan Clinical Research provides auditing services ensuring accuracy, integrity and quality of data and timeliness of the study. Farzan Clinical Research employs ICH-GCP guidelines as a quality benchmark for audits from study start-up to database lock in a trial.