Next-Gen Clinical Trial Compliance

Accelerate Research with AI Intelligence

Transform your clinical trials with real-time monitoring and AI-driven insights. Ensure participant compliance while reducing costs by up to 40%.

Schedule a Demo How It Works
HIPAA Compliant
SOC2 Ready
Trialsights App Interface
40%
Cost Reduction
2x
Faster Processing
24/7
Real-time Monitoring

Why Choose Trialsights

Everything you need to run compliant trials

Leverage AI technology to ensure compliance, reduce risks, and accelerate research outcomes with our comprehensive platform.

Real-time Compliance Monitoring

Advanced AI algorithms track participant adherence and flag potential compliance issues before they impact your trial.

Mobile Participant Engagement

User-friendly mobile app keeps participants connected and engaged throughout the trial process.

Intelligent Analytics Dashboard

Comprehensive insights for labs and sponsors with predictive analytics and compliance trends.

Cost-Effective Solution

Reduce monitoring costs while improving data quality and participant retention.

Audit-Ready Security

Enterprise-Grade Security & Compliance

We understand that data security is paramount in clinical research. Our platform is built from the ground up to exceed global regulatory standards.

FDA 21 CFR Part 11 Ready

Designed for full compliance with electronic record and signature requirements, including audit trails and data integrity controls.

HIPAA & GDPR Ready

Built-in privacy controls and architecture designed to protect PHI and assist with your data protection compliance obligations.

SOC 2 Type II Ready

Built with security controls derived from SOC 2 Trust Services Criteria, ensuring robust security, availability, and confidentiality.

End-to-End Encryption

AES-256 encryption for data at rest and TLS 1.3 for data in transit, ensuring maximum information security.

Frequently Asked Questions

Common questions from clinical operations leaders about security, compliance, and implementation.

Is Trialsights compliant with FDA 21 CFR Part 11?
Our platform is designed to support 21 CFR Part 11 compliance. It includes all necessary technical controls for electronic records and signatures, such as audit trails, user authentication, and system validation capabilities.
How is participant data secured?
All data is encrypted at rest using AES-256 and in transit using TLS 1.3. Our architecture is built on SOC 2 Type II certified infrastructure, and our internal controls are designed to align with SOC 2 standards.
Can Trialsights integrate with our existing EDC system?
Absolutely. We offer seamless integration APIs for major Electronic Data Capture (EDC) systems, including Medidata Rave, Veeva Vault, and RedCap, ensuring smooth data flow without manual entry.
What is the typical implementation timeline?
Most study teams can go live within 2-4 weeks. Our dedicated customer success team handles the configuration, validation, and training process to ensure a rapid and compliant deployment.

Ready to Transform Your Clinical Trials?

Join leading research organizations using Trialsights to revolutionize trial compliance monitoring and data integrity.

Schedule Demo

No credit card required for demo • SOC2 Ready