ClinStream CTMS, designed for precision medicine and real-world research

The complete solution for all your trial management support needs, integrating study management, IP distribution, site management, data visualization and financial reporting.


Integrated study management at your finger tips — proven by 20 years of global use!

Modern trials draw on many software systems. Our ClinStream Cloud fluidly integrates these to provide finger-tip study management in the palm of your hand!


Streamline your data acquisition from all sources in real time

Combine eSite data, eLab data, ePRO data and key input from other sources in real time to enable continuous central monitoring and risk-based site monitoring.


     

Finger-tip Management

Modern trials draw on many separate software systems. ClinStream Cloud fluidly integrates data from all sources and enables overall study management, real-time randomization and IP management, site management, data visualization for in-stream analysis, study monitoring, and finger-tip financial control.


Rapid and scalable

Our highly-acclaimed simple and scalable ClinStream digital clinical research platform links investigators and clinical teams, patients and caregivers, health providers and purchasers for all clinical trials and health outcomes research independent of time or location.


Modular and flexible

Advanced modular and flexible design ensures that ClinStream adapts perfectly to every study for efficient management of document control, site management and investigator support, data management and verification, real-time analysis and reporting and financial control.



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Integrated study management - at your finger tips!

ClinStream Cloud CTMS - designed for personalized medicine and proven by 20 years of global use!

Modern trials draw on many separate software systems. Our ClinStream Cloud fluidly integrates data from all sources and enables overall study management, real-time randomization and IP management, site management, data visualization for in-stream analysis, study monitoring, and finger-tip financial control.


Study Module

Study Module monitors clinical trials and research study conduct, progress, management and monitoring, and supports the Executive Committee, Scientific Advisory Board, and Data Review Board and other functions.


Document Module

Document Module maintains essential clinical trials study documents and clinical research amendments in electronic format for easy version control, distribution, navigation, and retrieval.


Site Module

Site Module facilitates all aspects of study site management including screening and recruitment, GCP/GPP training and certification, investigator documents and TMF, continuous site evaluation and support, and activity-based reimbursement.


Data Module

Data Module provides interactive electronic case report forms for patient enrolment, randomization, data entry, queries and correction, with on-line checks for omissions and errors at the point of entry.


Report Module

Report Module maintains essential clinical trials study documents and clinical research amendments in electronic format for easy version control, distribution, navigation, and retrieval.


Client Module

Client Module provides all key data for smooth and efficient communications including monthly budget updates, discussions and minutes, and critical trial decisions for immediate access.