Next-gen clinical data management system (CDMS) solution
Leverage advanced clinical data management systems (CDMS) to provide high-quality data to streamline and accelerate faster drug discovery and time-to-market.
Stay ahead of the curve with next-gen clinical data management system
The evolution of the clinical research industry, over the last decade, has led to the development of advanced clinical data management systems. These systems enable real-time data integration, data standardization at different layers, risk-based monitoring, real-time data reviews, and advanced analytics for life sciences companies. Future-forward companies are adopting next-gen clinical data management system (CDMS) to:
- solve the clinical data aggregation and visibility constraints for better outcomes.
- provide robust controls to implement data quality and governance.
- enable data validations across clinical data sets as per business rules.
Leverage next-gen non-transactional, self-serve, and customizable clinical data management system for real-time data collection and aggregation. Extract data’s greatest value to streamline and fast-track drug discovery and time-to-market!
Read Article / 5 reasons for the switch from clinical data management to clinical data science
Next-gen clinical data management system solution
Robust data aggregation
Tailored semantic for complex business rules
Clinical decision support
Built to scale
Service offering
Key results
Business outcomes
- Agile clinical development
- Clinical development optimization
- Left shift of data services
- Meeting your needs with the next-gen CDMS
Customized and assembled platform with accelerators
Greater visibility and control over the data
Manage trials with agility and speed
Replace legacy systems and remove vendor lock-in
Digital trials
- Continuous and confidential collection of data and eSource information.
- Securely manage data sources and harmonize with performance analytics and remote monitoring.
- Reimagine the process to drive automation for clinical data, from protocol to submission.
Analyzing R&D strategy
- Global regulatory and compliance insight for fast regulatory approval.
Axtria clinical research hub
White Paper