Stay Ahead with Smarter Clinical Trial Compliance
Monitor, manage, and maintain regulatory compliance with precision. Our intelligent portal empowers Sponsors, CROs, and Sites to stay audit-ready and ensure ethical, transparent trial conduct.
Smarter Compliance for Clinical Trial
We simplify how Sponsors, CROs, and Sites manage complex regulations—reducing risk, improving efficiency, and ensuring audit readiness throughout the clinical trial lifecycle.
- Centralized Regulatory
- Automated Compliance Monitoring
- Streamlined Audit Readiness
- Role-Based Access Control
Key Features To Drive Clinical Trial Compliance Success
Our platform simplifies regulatory compliance for Sponsors, CROs, and Sites with automated checks and real-time dashboards—making audits and inspections faster, easier, and more efficient.
- Real-Time Compliance Dashboards
- Automated Regulatory Checks
- Instant Audit Trails
- Intelligent Alerts & Notifications
Seamless Compliance in Four Simple Steps
Our platform integrates with your systems, monitors compliance in real-time, flags potential risks, and generates audit-ready reports—making clinical trial compliance effortless and transparent.
Why Leading Clinical Trial Teams Trust Our Compliance Platform
We offer broad regulatory coverage, real-time monitoring, and smart automation—making compliance simple, secure, and audit-ready for Sponsors, CROs, and Sites.
Driving Global Trust with Proven Clinical Compliance
Trusted by global trial teams, our platform ensures secure data handling, consistent audit success, and compliance at every step.
FDA 21 CFR Part 11
Reliable records & eSignatures compliance.
GDPR
Safeguards EU data privacy.
HIPAA
Secure patient data & privacy.
GCP
Defines quality standards for trials.
CDSCO
Regulates drug and device approvals.
EU Annex 11
Sets rules for system data integrity.
FDA 21 CFR Part 11
Reliable records & eSignatures compliance.
GDPR
Safeguards EU data privacy.
HIPAA
Secure patient data & privacy.
GCP
Defines quality standards for trials.
CDSCO
Regulates drug and device approvals.
EU Annex 11
Sets rules for system data integrity.
Flexible Compliance Plans for Every Trial Team
From emerging biotech startups to global CROs, choose a plan that simplifies your compliance journey and scales with your clinical operations.
Starter Plan
Basic rule-based validation
Limited record/file checks
Manual uploads only
Error detection (basic)
Missing field alerts
Basic compliance indicators
Basic rule-based validation
Limited record/file checks
Manual uploads only
Error detection (basic)
Missing field alerts
Basic compliance indicators
Preferred Compliance Platform for Global Research
Trusted by pharmaceutical leaders, biotech innovators, global CROs, and top academic research institutions, our clinical trial compliance platform delivers accuracy, transparency, and regulatory compliance—accelerating audits, reducing risk, and driving successful trial outcomes.
Frequently Asked Questions
Find clear, comprehensive answers to the most frequently asked questions about our clinical trial compliance scanning platform.