21CFR Part 11 Compliant

NIV-DAS 3.0

Secure | Smart | Seamless

NIV-DAS is where the world of pharmaceutical chambers meets technology

Our cutting-edge, 21 CFR Part 11 compliant data acquisition software is designed to streamline your data collection and analysis process. Our powerful software is capable of gathering data from various sources in real-time, providing you with accurate, reliable and actionable insights.

Sample Tracking

Ensure complete sample traceability with seamless tracking throughout the entire study lifecycle

Notification System

Receive instant SMS and e-mail alerts for critical alarms in real time

Multi Department Creation

Enable structured, department-wise control for users, equipment, and data across your organization.

Complete Audit Trails

Capture every system activity with secure, time-stamped audit trails for total transparency and control.

Trend Analysis

Gain deeper operational insights through advanced trend analysis and graphical performance evaluation.

Advanced Security Features

Engineered with advanced security controls to safeguard sensitive data and critical operations.

Electronic Signature

Facilitate secure electronic approvals with enhanced authenticity, accountability, and compliance.

Web-based

Experience secure, browser-based access for convenient monitoring and control from anywhere on your network.

Custom User Rights

Customize user permissions with precision to ensure controlled access based on roles and responsibilities.

21 CFR Part 11 Compliant

Built to support regulatory expectations with features aligned to 21 CFR Part 11 compliance requirements.

Up to 16 Equipment

Centralize the monitoring and management of up to 20 equipment through a single powerful platform.

Automated Backup System

Protect valuable data with intelligent automated backups designed for reliability and continuity.

Inside NIV-DAS 3.0

Real-Time Equipment Intelligence

NIV-DAS 3.0 provides continuous visibility into equipment status, operational conditions, and alarm events to help teams respond faster and maintain uninterrupted monitoring workflows.

Unified Operational Visibility

NIV-DAS 3.0 centralizes chamber monitoring, alarm management, and environmental tracking into a single intuitive interface for faster decision-making and improved operational control.

Intelligent Data Trend Visualization

Monitor live and historical chamber performance through dynamic trend graphs that help identify deviations, optimize operations, and maintain complete data traceability.

Software Architecture

Why Pharmaceutical Teams Choose NIV-DAS?

Compared to conventional monitoring systems, NIV-DAS 3.0 delivers greater visibility, stronger compliance support, improved operational efficiency, and enhanced data integrity across critical environments.

Capability	Traditional Monitoring Systems	NIV-DAS 3.0
Centralized Monitoring	Limited or separate local systems	Unified monitoring across multiple chambers
21 CFR Part 11 Readiness	Partial or manual compliance processes	Designed for 21 CFR Part 11 compliance
Real-Time Data Access	Delayed or manual data retrieval	Live monitoring with instant visibility
Audit Trails	Limited event logging	Complete secure time-stamped audit trails
Electronic Signatures	Often unavailable	Secure electronic signature workflows
Alarm Notifications	Local alarms only	Software, SMS & email notifications
Data Integrity	Risk of manual intervention	Secure, traceable electronic records
User Access Control	Basic login systems	Role-based customizable permissions
Department Bifurcation	Single Dashboard	Multiple Department Creation and Segregation
Sample Tracking System	No Tracking Feature	In-built with Notifications
Trend Analysis	Manual reporting	Intelligent graphical trend analysis
Remote Accessibility	Restricted to local systems	Secure web-based access within network
Backup & Recovery	Manual backups	Automated backup architecture
Equipment Scalability	Difficult to expand	Supports monitoring of multiple equipment
Operational Visibility	Fragmented information	Centralized operational dashboard
Regulatory Readiness	Audit preparation intensive	Audit-ready reporting and traceability
Response to Deviations	Slower manual escalation	Real-time alerts for faster action

See how NIV-DAS helps improve your workflow and compliance

Connect with our experts to see a personalized demo and discover how NIV-DAS can simplify your compliance.

Datasheet

Download 21 CFR Part 11 White Paper

NIV-DAS 3.0 is designed for pharmaceutical environments where data integrity, traceability, and reliability are non-negotiable.