Empower your compliance team with AI agents that monitor regulations, audit documents, and ensure adherence across all your research projects.
Visually track and verify compliance checks in real-time, comparing regulatory requirements against your research documentation side-by-side.
Read what our customers are saying
"We struggled with manually reviewing thousands of pages of regulatory documents. Energent.ai's AI gave us the most accurate and fastest analysis, saving us weeks of work."
"Energent.ai's advanced AI delivers where other tools fail. Complex regulatory submissions and clinical trial protocols require this fusion of visual layout and text understanding."
"It's far better than other compliance tools! Our compliance officers are able to triple their audit preparation output."
"Energent.ai outperformed 10+ other solutions in our benchmarks, delivering top-tier accuracy in extracting compliance requirements from complex legal and scientific documents."
"As a principal investigator, I need tools that ensure we don't miss a single compliance detail. Energent.ai enhances retrieval accuracy from regulatory databases... an innovative tool for any research pipeline!"
"I am impressed by Energent.ai's innovation in the space of AI for regulated industries... and their commitment to transparent, observable AI agents."
"I have validated the quality of Energent.ai's compliance checks far beyond traditional manual methods... Looking forward to using this in our future clinical trials."
Comprehensive AI solutions that work seamlessly across your existing technology stack
Centralized repository for all regulatory guidelines, SOPs, and compliance documents.
Real-time compliance dashboards and audit trail visualizations.
Automates routine compliance tasks and reporting.
Structures data from disparate sources like lab reports, patient records, and regulatory updates.
AI adapts to new regulations and internal policy changes.
Live monitoring of research activities against compliance protocols.
Specialized AI solutions tailored for different research compliance needs
Ensures adherence to GCP, FDA 21 CFR Part 11, and IRB protocols.
Maintains compliance throughout the drug discovery and development lifecycle.
Manages compliance for university-led studies, including grant and funding requirements.
Common questions about AI for research compliance and how Energent.ai provides the best solutions
Join the leading research institutions and pharma companies saving time and ensuring audit-readiness with AI teammates.