India Pharma Award 2022
TCS ADD™ Connected Clinical Trial platform received recognition for providing a unified, next-gen patient and site-centric offering
TCS ADD™ Connected Clinical Trials
Modern. Scalable. Adaptive. Modular.
Products and Platforms
TCS ADD™
TCS ADD™: A Suite of Modern and Open Technology Platforms
Highlights
- 14+ Patents demonstrating innovation
- 19+ Global customers leveraging the solution
- 700+ Trials supported for enhanced efficiency
- 50K+ Sites onboarded for seamless operations
- 20+ Language support for a global reach
- 100% Regulatory compliance, ensuring adherence to industry standards
Overview
TCS ADD™ Connected Clinical Trials is a comprehensive digital platform designed to transform the clinical trial landscape by addressing critical operational inefficiencies and enhancing stakeholder engagement.
Built with a focus on streamlining trial operations, the platform empowers pharmaceutical organizations to seamlessly oversee every stage of patient recruitment, screening, and enrollment while also giving holistic visibility on patients' journeys through the trial. Its automated screening capabilities leverage predefined criteria to identify suitable participants efficiently, reducing manual effort and accelerating timelines.
The patient recruitment and trial team gain visibility into recruitment progress via real-time tracking, allowing for data-driven adjustments and proactive management to ensure on-time enrollment. The integrated communication tools foster direct, timely interactions between the recruiters, the trial team, and participants, eliminating silos and fostering meaningful engagement throughout the clinical trial journey.
TCS ADD™ Connected Clinical Trials also offers advanced data integration with other clinical trial management systems, enabling organizations to unify workflows related to data management, advanced analytics, and patient engagement. By prioritizing digital connectivity, as evident through features like digital consenting, online diary submissions, and a comprehensive patient dashboard, TCS ADD™ Connected Clinical Trials elevates both patient and site experiences, ensuring that modern clinical studies are more informed, collaborative, and effective than ever before.
Challenges
Pharmaceutical organizations today must navigate the dual imperative of delivering well-informed, patient-centered clinical trials while maximizing operational efficiency at trial sites. Legacy approaches, often characterized by fragmented systems and manual, paper-driven workflows, result in inefficiencies, delays, and suboptimal engagement for all stakeholders involved.
By contrast, a modern digital solution—built on comprehensive management of recruitment, automated screening, real-time tracking, integrated communication, seamless data integration, and advanced analytics—addresses these challenges head-on, streamlining processes and empowering both sponsors and sites to drive successful, timely clinical studies.
Key features
- Effective recruitment and enrollment: Efficiently manage patient recruitment, screening, and enrollment processes.
- Automated screening: Utilize automated tools to screen potential participants based on predefined criteria.
- Real-time tracking: Monitor recruitment progress in real-time, ensuring timely updates and adjustments.
- Seamless communication: Facilitate communication between recruiters and potential participants via integrated messaging systems.
- Data integration: Seamlessly integrate with other clinical trial management systems for a unified workflow.
- Analytics and reporting: Generate detailed reports and analytics to track recruitment performance and identify areas for improvement.
- Connected engagements: Enhance patient and site interactions via digital connectivity.
- AI-driven ethics submission: Automated package creation and verification for faster approvals.
- Proprietary patient and site app: BYOD-compatible for seamless access.
- Real-time actionable alerts: Enabled by wearables, smart blisters, bottles, and connected devices.
- Flexible eConsent options: Supports remote, traditional, and hybrid models with wet signatures or paper-based consent.
- Seamless integration and quick deployment: Easily connects with native systems for smooth adoption.
Our capabilities
- Site portal: A dedicated portal for clinical sites to manage trial activities, access resources, and communicate with sponsors and patients.
- Volunteer portal: A user-friendly portal for trial volunteers to track their participation, access study information, various questionnaires, perform consents, and provide feedback.
- Recruitment portal: A comprehensive portal for managing patient recruitment, screening, and enrollment processes.
- Supply management: Efficient tracking and distribution of trial supplies, ensuring timely delivery and optimal inventory levels.
- eCOA, diaries, and surveys: Digital tools for patient-reported outcomes and feedback, enhancing data accuracy and patient engagement.
- eConsent: Secure and compliant electronic informed consent process, streamlining patient onboarding and ensuring regulatory adherence.
- Telemedicine: Virtual consultations for remote patient engagement, providing convenient access to healthcare professionals and reducing travel burdens.
- Devices and wearables: Integration with medical devices for real-time data collection, enabling continuous monitoring and proactive interventions.
- Connected engagements: Enhancing patient and site interactions via digital connectivity, fostering better communication and collaboration.
Enabling a time-critical remote consent
TCS helped Roche roll out an eConsent solution
Modern technologies, deep contextual expertise, and close collaboration with pharma organizations, patient advocacy groups, regulatory bodies, clinicians, and others alike combined with an ability to support adaptive (virtual, traditional, and hybrid) studies make TCS ADD™ Connected Clinical Trials, our decentralized trials platform, a preferred choice for trials worldwide.
