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Decentralized Clinical Trials
At Seriant, we are powering the Future of Clinical Trials.
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We deliver cutting-edge Decentralized Clinical Trial (DCT) solutions that elevate the standards of high-quality research, ensuring efficiency, compliance, and patient-centric innovation.
We seamlessly integrate specialized technology, expert oversight, and patient-centric approaches to improve clinical trial efficiency without adding complexity. By reducing site burden, expanding study access, and ensuring real-time data integrity, we help sponsors optimize study execution while maintaining the highest regulatory standards.
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Our in-house developed DCT platform is a fully regulatory-compliant, scalable, and customizable solution that seamlessly integrates remote patient engagement, real-time data capture, and decentralized trial logistics to optimize study efficiency and compliance:
- eConsent— Secure, remote participant enrollment with enhanced compliance
- ePRO (electronic Participant-Reported Outcomes)— Direct participant engagement for real-time insights
- Telemedicine & Virtual Visits—Remote interactions between site personnel and study participants, when possible, to enhance the convenience of study participation
- eCOA (electronic Clinical Outcome Assessment)
- Patient Portal
- IWRS (Interactive Web Response System)— Randomization and supply chain automation, with direct to patient shipping
- Integration with in-house and third-party technologies & systems
- More coming soon!
Whether through our in-house technology, or in combination with our partners, we offer a combination of technology, regulatory expertise, operational efficiency, and patient engagement strategies to ensure smooth study execution and compliance
- Early-Stage Feasibility & Study Design Optimization— We assess protocol feasibility, patient accessibility, and regulatory considerations
- Vendor & Logistics Oversight via Secure, user-friendly digital platforms for remote data collection and monitoring
- Recommend the right Technology & Solutions to enhance patient participation and retention (i.e. wearables, mobile apps, and telehealth)
- Data security and privacy compliance (GDPR, HIPAA)
- Strong Project Management through every step of the project life cycle
We prioritize a patient-centric approach, designing trials that minimize participation burden through flexible options, proactive support, effective recruitment strategies, and tailored training to enhance both patient experience and retention.
- Patient-friendly trial design to reduce the burden of participation
- Impactful Patient Recruitment & Retention strategies
- Ongoing Patient Support & Communication
- Flexible Participation Options— Offer home visits, telehealth consultations, and hybrid site visits to accommodate patient needs
- Comprehensive Site & Patient Training, tailored to their needs
We ensure smooth connectivity across all systems, maintaining strong oversight of partners and technology while leveraging advanced monitoring, data insights, and compliance-driven platforms for secure and efficient trial execution.
- Seamless integration with in-house and third-party vendor systems
- Robust vendor & technology oversight
- Medical Data Review, central monitoring and risk-based monitoring solutions
- Analytics and data surveillance
- Secure & Regulatory-Compliant Platforms – Use-validated, 21 CFR Part 11, HIPAA, and GDPR
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