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Clinical Trial Management System

Image Features of a clinical trial management system are as given below :- The CTMS will provide an extensive range of functionality that will strengthen the conduct of both oncology and non-oncology clinical trials: CLINICAL RESEARCH MANAGEMENT The system enables management of many aspects of clinical research including: study start-up timelines, tracking and reporting of protocol information and accrual data, study financial management and billing compliance. BILLING COMPLIANCE The CTMS allows for shared study calendars, centralized & standardized billing processes including sponsor invoicing and subject visit tracking. INTEGRATIONS / INTERFACES The CTMS will integrate with Epic to facilitate patient data transfer from the clinic to the CTMS and will incorporate other study-related modules like ePRMS to support Scientific Review Committee processes. REPORTING / ANALYTICS The CTMS provides robust and streamlined reporting to meet NCI protocol and accrual reporting requirements, to support billing and financial operations, and to track trial start-up timelines.