Business and GxP compliant solutions, services by SarjenBusiness and GxP compliant solutions, services by SarjenBusiness and GxP compliant solutions, services by Sarjen

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

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
PM dashboard

eTMF

Clinical trials documents – upload and review

  • Centralized, compliant document repository
  • Version control and role-based access
  • Automated workflows with audit trails
eDC LP

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

ePRO

Patient questionnaires – entry and review

  • Patient diaries with multilingual access
  • Flexible surveys, real-time syncing
  • Engagement tools for better retention
MI LP

MI LP

Image uploading and analysis

  • DICOM uploads with secure transfers
  • Smart lesion measurement tools
  • Multi-role grading and annotations
PDMS

PDMS

Protocol deviations – entry and review

  • Auto alerts for deviation logging
  • Categorization by type and severity
  • Root cause analysis and CAPA tracking

Share your protocol, let us build your solution

Features

21 CFR Part 11 & GCP compliant

Seamless Automations

Globally aligned & audit ready always

user friendly

Quick ROI with fast setup in under 12 weeks

Intelligent Data Provision

Intelligent & automated workflows for productivity

Configured as per your protocol

Designed for scalability and reliability

Other domains served by Sarjen

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