Syreon Corporation
Syreon is a global leader in clinical research, health economics, outcomes research, computational analysis, and real-world evidence research, specializing in complex and chronic diseases. Driven by senior researchers, Syreon collaborates with top pharmaceutical companies, biotech firms, academia, and healthcare providers worldwide to evaluate new treatments, demonstrate value, and guide safe and cost-effective clinical use. With over 30 years of experience, Syreon excels in precision medicine, post-marketing surveillance, personalized care, and innovative clinical trial designs, leveraging digital networks and computational medicine to streamline health sciences research and improve patient outcomes.
Industries
Nr. of Employees
medium (51-250)
Syreon Corporation
Products
Cloud clinical trial management system (CTMS)
A cloud-based CTMS that integrates EDC, eLab and ePRO data, supports online randomization and IP management, provides site and document controls, in-stream data visualization and financial management.
Cloud clinical trial management system (CTMS)
A cloud-based CTMS that integrates EDC, eLab and ePRO data, supports online randomization and IP management, provides site and document controls, in-stream data visualization and financial management.
Services
Clinical trial design and adaptive trial consulting
Design and planning of Phase I–IV trials using adaptive, umbrella/basket and biomarker-driven approaches.
Project management and study operations
Operational management of global clinical programs including project management, site management and study monitoring.
Data management and EDC/ePRO implementation
Database programming, single-point entry or automated uploads, data processing, coding, queries, and 21 CFR Part 11–compliant systems.
Cloud-based clinical research platform deployment
Deployment and configuration of a cloud CTMS to integrate eSite/eLab/ePRO data, enable real-time randomization, IP management, site and document control, in-stream analysis and financial management.
Centralized and risk-based monitoring
Selection and implementation of centralized monitoring and risk-based site monitoring strategies using advanced data analytics.
Statistical analysis and pharmacometrics
Adaptive trial simulations, interim and final analyses, PK/PD modeling, genomic and economic analyses and DSMB support.
Clinical trial design and adaptive trial consulting
Design and planning of Phase I–IV trials using adaptive, umbrella/basket and biomarker-driven approaches.
Project management and study operations
Operational management of global clinical programs including project management, site management and study monitoring.
Data management and EDC/ePRO implementation
Database programming, single-point entry or automated uploads, data processing, coding, queries, and 21 CFR Part 11–compliant systems.
Cloud-based clinical research platform deployment
Deployment and configuration of a cloud CTMS to integrate eSite/eLab/ePRO data, enable real-time randomization, IP management, site and document control, in-stream analysis and financial management.
Centralized and risk-based monitoring
Selection and implementation of centralized monitoring and risk-based site monitoring strategies using advanced data analytics.
Statistical analysis and pharmacometrics
Adaptive trial simulations, interim and final analyses, PK/PD modeling, genomic and economic analyses and DSMB support.
Expertise Areas
- Clinical trial management
- Adaptive and precision medicine trials
- Digital health and clinical informatics
- Real-world evidence generation and analysis
Key Technologies
- Cloud-based CTMS and trial integration
- Electronic data capture (EDC) and ePRO systems
- CDISC data standards
- Genomics and targeted proteomics