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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

PM Dashboard
Clinical trial data representation and reports
Real-time visual project insights
Role-wise metrics and site tracking
Integrated study milestone dashboards

IPSM
IP dispensing and management
Real-time drug inventory tracking
Auto reordering and expiry management
Seamless site-to-CRO collaboration

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

PDMS
Protocol Deviations - Entry and Review
Auto alerts for deviation logging
Categorization by type and severity
Root cause analysis and CAPA tracking

MI LP
Image Uploading and Analysis
DICOM uploads with secure transfers
Smart lesion measurement tools
Multi-role grading and annotations
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
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