AI Agents That Work Inside Pharma Operations
AgentNX automates your most time-consuming compliance and manufacturing tasks — deviation reports, batch records, SOPs — so your team can focus on what matters.
Join the WaitlistStop Wasting Hours on Paperwork
Deviation Reports
Auto-draft GMP deviation reports from incident inputs. Review and sign off in minutes, not hours.
Batch Records
Generate and validate batch manufacturing records with full traceability and 21 CFR Part 11 compliance.
SOP Authoring
Create and update Standard Operating Procedures from process descriptions — formatted and audit-ready.
Why AgentNX?
Built by pharma IT professionals who lived these problems firsthand.
Designed with 21 CFR Part 11 and GMP compliance in mind from day one.
Cut documentation time from hours to minutes on every deviation or batch record.
Simple web interface — your QA and ops teams can use it without any training.
Get Early Access
We're onboarding a small group of pharma and biotech teams first. Join the waitlist to be first in line.