Compliance
Engineered In.
Protect your license to operate. Complete Electronic Batch Records (EBR), immutable audit trails, and strict QC quarantine gates are built into the ERP core — not bolted on.
GMP Compliance Built Into Every Workflow
Electronic Batch Records
Paperless BMR/BPR tracking with digital approvals. E-signatures are tied directly to shop floor operator IDs and roles for complete accountability.
QC Quarantine Gates
API and excipient inventory stays locked in "Quarantine" status until explicitly released by the QA officer. No production order can consume unreleased stock.
21 CFR Part 11 Audit Log
Every system action — edits, approvals, overrides — is captured in an immutable, time-stamped audit trail. Exportable for regulatory inspections at any time.
Lot Traceability
Full forward and backward traceability across all raw materials, in-process semi-finished goods, and finished packs. One click for any deviation investigation.
Stability & Retest Management
Automatically flag batches approaching retest dates. Schedule stability studies and maintain linked COA documents within the ERP record.
AI Process Analytics
Detect yield deviations across batches in real time. ML models flag out-of-trend (OOT) parameters before they become out-of-specification (OOS) events.
An Integrated Platform for Regulated Manufacturing
Pharma Clients Pass Audits First Time, Every Time
Immutable audit trails, fully digital BMR records, and role-based e-signatures mean your inspectors find everything they need — cleanly documented and instantly accessible.
See Compliance Demo →Ready to Strengthen Your Pharma Compliance?
Talk to our pharma domain specialists and get a compliance-focused ERP walkthrough.