BMRiq is the AI-powered Batch Manufacturing Record platform that connects SAP, IoT devices, and GMP workflows — eliminating paper, manual entry, and compliance risk.
Every paper-based batch record is a ticking compliance clock. Here's what pharmaceutical manufacturers lose every year because of manual documentation.
Illegible handwriting, missed mandatory fields, and incorrect calculations create data integrity violations that trigger FDA warning letters.
Physical routing of paper documents between departments adds 2–5 days to every batch release cycle, delaying time-to-market and revenue.
Manual record searching takes days of preparation before FDA, WHO, or CDSCO inspections — with no guarantee of completeness or accuracy.
BMRiq is purpose-built for pharmaceutical and FMCG manufacturing. Every feature exists because GMP requires it — not because a product manager thought it was cool.
10-stage batch execution from dispensing to final inspection. Every parameter entry validated against BMR spec limits in real time. No blank fields, no missed signatures.
GMP Stage 1–10Password re-authentication + mandatory reason for every QA approval and batch release. Immutable signature records with timestamp, IP, and cryptographic hash.
21 CFR Part 11MQTT-connected FBD, tablet press, granulator, coating pan, and balance instruments stream parameters directly into the BMR.
MQTT · OPC-UA · LIMSBatch initiation from SAP Production Order. BOM from SAP Recipe. Material lots from SAP Goods Issue. Yield auto-posted to SAP CO15 on QA approval.
SAP PP-PI · QM · PMStructured deviation creation with severity classification. Auto-generated CAPA with owner assignment, SLA tracking, and closure e-signature.
ICH Q10 · CAPAComplete batch dossier generated in under 30 seconds. Audit trail with every field change, user ID, timestamp, and IP address.
ALCOA+ · Audit readyBMRiq sits between SAP, your shop floor, and your QA team — connecting all three without a single manual data entry point.
SAP Production Order triggers BMRiq via API. Batch record auto-created with BOM and product data.
SAP PP-PI10 manufacturing stages with IoT instruments streaming every parameter directly into the BMR.
MQTT · OPC-UAOne-click e-signature approval with 21 CFR Part 11 credential re-authentication.
21 CFR Part 11BMRiq auto-posts yield and confirmation back to SAP. No manual CO15 entry.
SAP CO15 · QA11"We went from 4 days of QA approval routing to same-day batch release. The audit trail alone saved us 3 weeks of preparation before our last FDA pre-approval inspection."
"The SAP integration is seamless. Our production order releases in SAP and within seconds the batch is live in BMRiq with the BOM pre-filled. Operators have zero manual data entry."
"CDSCO audit last month — the inspector asked for batch records going back 2 years. We generated the complete dossier in 28 seconds. The inspector had never seen anything like it."
Book a 30-minute live demo with our pharma implementation team. We'll walk through your specific batch manufacturing process and show how BMRiq maps to your SAP and equipment setup.
We'll confirm within 4 business hours with a calendar link.