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Description
Accelerate clinical innovation with an AI-enabled Clinical Research Platform designed to unify Early Phase CTMS, Late Phase CTMS, and Bioanalytical LIMS into a single, intelligent ecosystem. Built for pharmaceutical, biotechnology, CRO, and research organizations, the platform supports the complete clinical development lifecycle—from protocol planning, volunteer and patient management, site operations, and subject scheduling to sample lifecycle management, bioanalytical testing, data review, and regulatory submissions.By connecting clinical and laboratory operations on a centralized platform, organizations gain real-time visibility, standardized workflows, and end-to-end traceability across studies. AI-enabled capabilities deliver intelligent workflow automation, predictive analytics, smart data validation, anomaly detection, and actionable insights that help research teams identify risks early, optimize resource utilization, reduce manual effort, and make faster, data-driven decisions. Automated alerts, configurable dashboards, and role-based workflows improve operational efficiency while ensuring data integrity and study oversight.Designed to support GxP, GLP, GCP, and 21 CFR Part 11 compliance, the platform provides comprehensive audit trails, electronic records and signatures, secure data management, and seamless interoperability with enterprise systems such as EDC, eTMF, ERP, and laboratory instruments. Its scalable, configurable architecture adapts to diverse study designs and organizational needs, enabling sponsors and CROs to streamline clinical operations, shorten study timelines, enhance collaboration, and deliver high-quality, inspection-ready data with confidence.
Description
Only SAS offers a comprehensive, cloud-native environment for statistical computing in clinical research, featuring built-in analytic tools, adherence to data standards, and optional integrated analytic applications. This foundation enhances your capacity to modernize processes and expedite the introduction of new therapies into the market, ultimately contributing to improved health outcomes. By utilizing a collaborative platform, you can effectively manage and analyze information, streamline procedures, and provide trial results more efficiently to regulatory bodies. It serves as a unified solution for clinical analysis and submission, encompassing all necessary components for validation, compliance with regulations, version control, audit trails, and documentation assistance. The platform facilitates automation through customizable workflows, supports current and forthcoming integrations, and ensures the implementation and management of data standards and controlled terminology. Additionally, it features a central hub for all incoming data, automates data quality assessments, enhances data management practices, and prepares analytical data with greater accuracy, thus enabling more insightful outcomes. Ultimately, SAS equips clinical researchers with the tools needed to navigate the complexities of modern research and regulatory environments effectively.
API Access
Has API
API Access
Has API
Integrations
Python
R
Pricing Details
$79
Free Trial
Free Version
Pricing Details
No price information available.
Free Trial
Free Version
Deployment
Web-Based
On-Premises
iPhone App
iPad App
Android App
Windows
Mac
Linux
Chromebook
Deployment
Web-Based
On-Premises
iPhone App
iPad App
Android App
Windows
Mac
Linux
Chromebook
Customer Support
Business Hours
Live Rep (24/7)
Online Support
Customer Support
Business Hours
Live Rep (24/7)
Online Support
Types of Training
Training Docs
Webinars
Live Training (Online)
In Person
Types of Training
Training Docs
Webinars
Live Training (Online)
In Person
Vendor Details
Company Name
Sarjen Systems Pvt Ltd
Founded
1998
Country
India
Website
biznet.sarjen.com
Vendor Details
Company Name
SAS
Country
United States
Website
www.sas.com/en_us/software/life-science-analytics-framework.html
Product Features
Clinical Trial Management
21 CFR Part 11 Compliance
Document Management
Electronic Data Capture
Enrollment Management
HIPAA Compliant
Monitoring
Patient Database
Recruiting Management
Scheduling
Study Planning