Clinical Trial Services

ClinTrial provides a comprehensive portfolio of services covering all phases of clinical research. ClinTrial conducts all clinical monitoring and related activities under GCP standards and in accordance with applicable law.

Clinical studies

Phase I-IV domestic and multinational trials

• Study design, protocol development, case report form design and printing
• Site and investigator selection and recruitment
• Regulatory and ethical approval procurement, preparation and review of regulatory submissions, interaction with regulatory agency
• Continuous liaison with investigators
• Management of patient recruitment
• Site management and monitoring based on Standard Operating Procedures and study-specific check-lists (site initiation, regular monitoring visits, source data verification, monitoring visit reports, adverse event reports, site closure visits)
• Data management services and trial administration (validated data entry, database design, data upload, computerised error detection and data checking, data queries, filing system design and implementation)
• Electronic information systems (investigator’s information, data handling guidelines, online status reports)
• Statistical evaluation
• Interim status report, final report and media presentation

Clinical pharmacological investigation site

• Phase I unit available through our sister company

Clinical testing of medical equipment

• Prosthetic devices
• Vessel grafts
• Machinery and equipment
• Bandages
• Blood sampling tools, needles, syringes
• Implants
• Plastic surgery applications

Pharmacovigilance

• Design, implementation and maintenance of drug safety reporting systems
• GCP compliance monitoring of all aspects related to trial drug