GMP · 21 CFR Part 11 · EU Annex 11
Quality release, without the paper trail.
JBRMS is a precision release-management system built for pharmaceutical manufacturing. Every batch, every signature, every deviation — traceable from line to license.
Built for the batch record, end to end
Electronic batch release
Sign and release batches with full e-signature audit trails, compliant from day one.
Deviation & CAPA
Capture, investigate, and close deviations with linked corrective actions and effectiveness checks.
Full audit readiness
Every action timestamped, attributed, and exportable. Walk into any inspection prepared.
Compliance, by design
JBRMS is engineered against the standards your regulator already expects — no retrofit, no patchwork.
GMP 21 CFR Part 11 EU GMP Annex 11 GAMP 5 ISO 9001
See JBRMS in your plant
Tell us about your release workflow and we'll show you how JBRMS fits.
hello@jbrms.io