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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.
Clinical Monitoring
With Seriant, You Gain More Than Just Monitoring.
We believe that successful clinical trials start with strong site relationships and personalized support.
Our Clinical Research Associates (CRAs) are a trusted extension of your team, focused on building and maintaining site engagement while upholding the highest standards in clinical research. With real-time insights from the ground, our team ensures high compliance levels and an unwavering commitment to patient safety.
- We go beyond monitoring; we partner with sites to ensure they fully understand study goals, timelines, and best practices for high-quality data collection.
- Our expert CRAs provide customized support, addressing medical, scientific, and operational challenges to set each site up for success.
- With a global network of clinical sites managed from our headquarters in Montreal, we ensure trials run efficiently and with the highest data integrity, fostering long-term relationships built on trust and collaboration.
- Our hands-on approach ensures that every site receives tailored 1:1 guidance from protocol training and recruitment strategies to navigating the latest technologies and innovations.
Timing is everything. Our CRAs bring extensive expertise across all study phases and therapeutic areas, ensuring seamless execution.
- Experienced CRAs guiding sites through all study phases
- Site selection & qualification
- Recruitment & enrollment support
- Study conduct & compliance
- Agile execution to meet critical deadlines
- Trial Closeout
At Seriant, we provide adaptive monitoring strategies tailored to the unique needs of each study and sponsor. Our expert team ensures that your trial remains on track while maintaining the highest standards of data integrity and compliance.
- Remote, on-site, and centralized monitoring tailored to study needs
- Data integrity & surveillance at every stage
- Strategic recommendations for the most effective monitoring solution
- Optimized oversight to reduce risk and enhance trial efficiency
We understand that the success of your clinical trial hinges on rigorous oversight, seamless site coordination, and a commitment to data integrity. That's why we implement robust controls and oversight, to ensure excellence in every aspect of our delivery.
- The right CRAs for the right study, leveraging their specific areas of expertise
- Real-time reporting & analytics for full transparency
- Strong oversight, metrics, Key Performance Indicators (KPIs)
Interested in this service?
Let’s work together!
