Our Mission
To simplify and strengthen clinical trials compliance through automation and actionable insights.
Simplify Workflows
Automate routine tasks to save time and reduce errors in trials operations.
Empower Organizations
Help Sponsors, CROs, and Sites stay audit-ready and confident.
Strengthen Processes
Ensure accuracy and reliability across all compliance activities.
Reduce Manual Effort
Automate repetitive tasks with smart, technology-driven solutions.
Our Vision
A future where clinical trials readiness is seamless, proactive, and technology driven.
Seamless Experience
Deliver user-friendly compliance processes for trials teams.
Trust & Transparency
Confidence with secure, efficient workflows and clear oversight.
Proactive Readiness
Anticipate regulatory needs before they become challenges.
Future Innovation
Continuously evolve compliance through modern technologies.
Our platform supports frameworks to help you stay audit-ready.
Our platform centralizes compliance with global frameworks, keeping you audit-ready.
- HIPAA
- GDPR
- 21 CFR Part 11
- CDSCO
- WHO-GMP
- EMA
Core Features That Power Clinical Trials Compliance
Document Management
- Upload and store compliance documents securely.
- Supports version control for accuracy.
- Enables e-signatures for approvals.
Audit Trails
- Automatically logs all user actions.
- Maintains transparency and accountability.
- Essential for regulatory inspections.
Training & SOPs
- Assign training modules and SOPs to users.
- Track completion and progress in real time.
- Certify compliance readiness of staff.
CAPA & Risk Management
- Track deviations and incidents effectively.
- Implement corrective and preventive actions.
- Manage risks with structured workflows.
Regulatory Alerts
- Real-time updates on new changed regulations.
- Automatic notifications for critical deadlines.
- Helps stay proactive and compliant.
Dashboards & Reports
- Visualize compliance status with clear metrics.
- Generate audit-ready reports instantly.
- Provides management insights at a glance.