At OCT we aim at the quality of the data and results on every stage of clinical trial conduct. Both the utmost accuracy of data we provide and compliance to GCP and country-specific regulatory requirements are key aspects of due diligence for us.
OCT QA Department takes the lead in maintaining SOPs, conducting QA of sites and subcontractors and implementing OCTs training policy. Our Head of Quality Assurance has an experience of 10 years in this field and is a certified BARQA Member, assuring the highest standards of OCTs ongoing quality control in accordance with GCP and applicable SOPs.
Among other duties QA Department is responsible for organizing Sponsors Audits.
While staying in the country of research, the client representative or auditor receives:
- a fully equipped workplace;
- phone, fax, postal services;
- high-speed Internet connection;
- professional interpreter;
- assistance during all visits to research centers and any other meetings.
