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The MHICC is now Seriant !
The Montreal Health Innovations Coordinating Center (MHICC) is now Seriant.
Our new name reflects a bold step forward— expanding beyond cardiology and embracing innovations in clinical trials with a global reach.
While our identity has evolved, our commitment to operational excellence, client satisfaction, and quality remains the same.
Decentralized Clinical Trials
At Seriant, we are powering the Future of Clinical Trials.
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.
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
Interested in this service?
Let’s work together!
