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
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.

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