We support clinical trial data, electronic health records, patient registries, real-world evidence datasets, and other regulated pharmaceutical data sources with full HIPAA compliance.

 Our platform provides expert-validated HIPAA compliance with continuous monitoring, automated risk assessments, and detailed audit trails that meet FDA and other regulatory standards

Yes, we seamlessly integrate with clinical data management systems, electronic data capture platforms, and other pharmaceutical technology stacks through secure APIs.

Most pharmaceutical implementations are completed within days, with Expert Determinations and compliance assessments typically finished in 2-3 business days.

Integral automates what traditionally takes months of manual consulting work, providing the same expert-level compliance validation in days rather than months.

Our platform generates comprehensive compliance documentation and audit trails that directly support regulatory submissions and FDA data integrity requirements.