Your protocol, our solution
Smart Trial Suite simplifies late-phase trials with flexible, protocol-adaptive systems and compliance-focused tools. Designed to meet diverse trial needs, it ensures smooth operations and customised support for every step of the process.
Sarjen System’s Smart Trial Suite is an advanced clinical trial management software for late-phase trials, built to speed up trials and reduce operational costs. It streamlines execution for maximum efficiency, enhances patient safety, and accelerates response times. With intelligent automation, it ensures compliance, delivers consistent trial outcomes, and improves the patient experience for better adherence. Equipped with real-time insights and seamless sponsor collaboration, Smart Trial Suite empowers smarter decisions and efficient trial management.
What makes Late phase clinical trials by Sarjen stand out?
Gateway
Access to various STS softwares
IPSM
IP dispensing and management
- Real-time drug inventory tracking
- Auto reordering and expiry management
- Seamless site-to-CRO collaboration
PM Dashboard
Clinical trial data representation and reports
- Real-time visual project insights
- Role-wise metrics and site tracking
- Integrated study milestone dashboards
PRMS
Patient recruitment and randomisation
- Dynamic enrolment with stratified randomisation
- Visit scheduling with real-time alerts
- Audit trail for every query raised
eTMF
Clinical trials documents – upload and review
- Centralized, compliant document repository
- Version control and role-based access
- Automated workflows with audit trails
EDC LP
Clinical trials data/information gathering
- Direct data capture from devices
- Real-time edit checks and validations
- Role-based access and page reviews
ePRO
Patient questionnaires – entry and review
- Patient diaries with multilingual access
- Flexible surveys, real-time syncing
- Engagement tools for better retention
MI LP
Image uploading and analysis
- DICOM uploads with secure transfers
- Smart lesion measurement tools
- Multi-role grading and annotations
PDMS
Protocol deviations – entry and review
- Auto alerts for deviation logging
- Categorization by type and severity
- Root cause analysis and CAPA tracking
Explore the Late Phase CTMS in detail
Features
21 CFR Part 11 & GCP compliant
Globally aligned & audit ready always
Quick ROI with fast setup in under 12 weeks
Intelligent & automated workflows for productivity
Configured as per your protocol
Designed for scalability and reliability
Other domains served by Sarjen
Clinical Research
Pharmacovigilance
Regulatory
Quality
Manufacturing
