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