AI-Native Life Science Regulatory Documentation Generation and Submission Platform
Angelonia AI transforms how life sciences teams prepare regulatory submissions. Specialized in pre-clinical in vitro and in vivo life sciences, it converts raw experimental data into polished, submission-ready documents — from Word reports and Module 4 eCTD packages to Module 2 and 3 summaries and the Investigator's Brochure (IB).
Built from the ground up for FDA 21 CFR Part 11 and GxP compliance, Angelonia AI ensures data integrity, system security, full traceability, and end-to-end auditability across every submission.
Angelonia AI allows your team spend less time drafting documents and formatting documentations, allowing scientists and clinicians more time on science.
We are here to help Subject Matter Experts thrive in their jobs.
Scientists/SMEs spend ~30% of their time writing documents which do not enjoy.
With our platform, SMEs hand off the drafting to AI. You direct the AI to author, then only focus on review and QC.
What do current customers say: ” After using Angelonia Technical Report Writing Tool, I no longer need to write any reports myself. I only need to review them. It has saved me so much time! A report that used to take me 3 weeks to from authoring to completion now only take me 3 hours. “ — VP, Head of DMPK
We enhance your confidence of your regulatory submission.
70% cost reduction comparing to traditional method
3x faster timeline from document generation to submission ready
90% less error in 1st draft compare to traditional manual workflow - higher quality
What do current customers say: "INDaccel transformed IND submission workflow. I love the the feature that enabling trace the data to the source document. It greatly accelerate the speed of doing the QC. What used to take our team 6 months now takes 4-6 weeks." — VP, Regulatory Affairs
Trusted by Subject Matter Experts
Biotech Companies & Academic Institutions
Cost Effective
Rapid Deployment
Higher Confidence in documentation and submission
Medical Writers & SME Consultants
Deliver more to clients with less human effort
Fewer revision loops
Ease with multi-clients management
CDMO & Large Pharma
Company-specific fine tuning
Portfolio-Scale
More Time for Strategy
Augment Subject Matter Experts’ capabilities by leveraging AI in Document Generation.
SMEs direct the AI to draft documents, then review with confidence using built-in traceability to the original source data.