An integrated healthcare platform that provides intelligent automation and data integration for clinical trials, improving drug development time-to-market for pharmaceutical companies
Wipro’s Digital Integrated Clinical Enterprise (DICE) platform is reshaping experiences for patients and healthcare providers in medical safety during clinical trials. The integrated healthcare platform provides a single source of truth for electronic data capture, electronic health records, clinical trial planning, clinical trial management and clinical trial analytics. It employs web-based patient encounters to enable virtual visits for intelligent clinical trials, uses IoT-enabled wearable sensors to securely collect patient telemetry, and obtains electronic consent in a patient-friendly and compliant manner.
Pharmaceutical companies can now leverage design and crowdsourcing to decrease their data entry and maintenance burden while increasing the speed of patient recruitment, optimizing clinical trial design, and ensuring risk based quality management, all in one place. With our cloud-based integrated healthcare platform for clinical trials, pharmaceutical companies can deploy intelligent automation and integrate data across the clinical trials process. They can transparently track metrics, optimize study budgets, and deploy outcome-based pricing and funding models, promoting informed decision making between site administrators, clinical trial sponsors, and investigators for pharmaceutical companies.
Wipro has partnered with Medidata, a global leader in clinical trials cloud software as a service. Our comprehensive suite of managed services and solutions available on Medidata’s clinical trial platform provide end-to-end support and intelligent automation to pharmaceutical companies on study initiation, study build, and data management and closure. These solutions enable improved decision making through efficient data management for pharmaceutical companies across the globe.
Wipro has a cadre of certified Medidata Rave Clinical Cloud™ consultants, this includes Medidata's Patient Cloud, Rave Study Build, Data Management and Data Validation consultants to support the full lifecycle of clinical trials operations and data management. By using these clinical trials software modules, pharmaceutical companies can reduce up to 64% of the study build time, have 44% faster database lock cycle times and reduce up to 80% data correction rates.