AI-Assisted QMS Documentation for Pharma & Nutraceuticals
Create, review and trace GMP documentation with regulatory-grounded AI assistance.
DocuCraft AI provides AI-assisted documentation and regulatory support. It does not replace qualified QA/RA/legal review or a company's approved QMS procedures. AI-generated documents must be reviewed and approved according to the user's applicable quality system before regulated use.
Built around how quality teams actually work
Regulatory Library
Search verified and clearly labelled sources for India, US, EU, WHO and PIC/S requirements.
DOCX & PDF export
Export saved drafts with document metadata and a clear AI-assisted draft disclaimer.
30+ QMS document types
SOPs, STPs, deviations, CAPAs, OOS/OOT, validation and qualification protocols, and more.
Regulatory context
Schedule M, WHO GMP, EU GMP, US FDA 21 CFR, ICH and FSSAI frameworks mapped by document type.
Personal & business workspaces
Work solo or inside an organisation with role-based access and strict data isolation.
Private by design
Row-level security means your records are only ever visible to you and your organisation.
AI-assisted drafting
Structured first drafts with regulatory references you refine — never a substitute for your own review.
Full audit trail
Every create, update and status change is recorded with a timestamped activity log.
Start with the Personal plan
₹599 per month after a 7-day free trial. Includes normal professional AI use, all supported document types, saved history, Regulatory Library access, and DOCX/PDF export.
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