Document Lifecycle Management
- Automated document creation and routing
- Version control with change tracking
- Review and approval workflows
- Document retirement and archiving
AI-Powered Document Analysis and Compliance Verification: Document Control
Manage versions, ownership, status and FDA Part 11 e-signatures.
Use AI agents to systematically check all documents and data in your corpus for discrepancies, compliance risks, and standardization gaps with unprecedented thoroughness.
- Version, status and ownership visible
- Review history attached
- Ready for submission or inspection
See it on your documents
Book a DemoEnterprise Integration
Works with the tools your team already uses
Sanai connects to Word, SharePoint, Veeva, Benchling and the rest of your stack, so there is no data migration.
Microsoft Word
Google Drive
SharePoint
Dropbox
Box
OneDrive
Google Docs
Microsoft Teams
Slack
Jira
Confluence
Okta
Microsoft Entra ID
Google Workspace
Snowflake
Databricks
Amazon S3
Veeva Vault
Benchling
LabWare LIMS
MasterControl- ODOpenText Documentum
- STSparta TrackWise
LabVantage
IDBS
Thermo Fisher SampleManager
Medidata Rave
Oracle Clinical One- RREDCap
- Veeva CTMS
PubMed- EEndNote
Zotero
Solutions
Built for every team
Each team in life sciences has unique workflows. Sanai adapts to your specific needs across medical writing, regulatory affairs, manufacturing, and more.
IND and BLA sections with a traceable line
from every claim to its source.
Quality policies, SOPs and standard test methods
drafted to your standards, then checked against them.
Module 3, process development and validation reports built from your batch and assay data.
Learn MoreClinical study reports, protocols and investigator brochures drafted from your data, cited claim by claim.
Learn MoreMedical information responses grounded
in your approved source documents.
Find prior study results across every system
before you design the next study.