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Dynamic Electronic Batch Record (eBR) Execution Engine
Novaqis BRM is electronic batch record software for pharmaceutical manufacturing. Operators execute master formulas on plant tablets with Critical Process Parameter limits, 21 CFR Part 11 e-signatures, eLog line-clearance handshake, and Review-by-Exception QA release—replacing paper binders that delay disposition.
Dashboard / Manufacturing
Dashboard
Recent batches
At a glance
Enterprise Architecture
Deterministic architectures and automated compliance engines engineered for multi-plant pharma operations.
Publish governed master formulas with version control and parameter limit gating, guiding operators through every run on plant floor tablets under 21 CFR Part 11 electronic signatures.
Enforce soft and hard limit validation rules during execution. Soft breaches require mandatory justification comments, while hard breaches trigger immediate quality deviations.
Zero line clearance bypass: BRM queries Novaqis eLog via typed HTTP integration to verify cleanroom and equipment status, clean-hold validity countdowns, and containment locks before initiating any batch run.
Real-time query of released and unexpired lots from Novaqis ERP; automated material consumption stock entry creation on dispense; and finished goods batch creation on QA release.
Automated QA dashboard aggregates analytical results, critical process parameter limits, and deviation flags, compressing final batch disposition from 3 days to under 2 hours.
Real-time interlocks block uncertified operators from executing critical manufacturing steps, preventing 483 findings for personnel training non-compliance.
Deploy on dedicated validated private cloud (AWS/Azure/GCP) or 100% sovereign air-gapped on-premises plant infrastructure with offline ES256 cryptographic licensing.
In the product
Execute digital master formula recipes with real-time Critical Process Parameter (CPP) interlocks, pre-flight eLog cleanroom handshakes, 2D material barcode scanning, and review-by-exception QA release.
eBMR
Electronic batch execution
MFR
Master formula records
CPP
Process limit interlocks
ERP
Live material issue sync
Dynamic Electronic Batch Record (eBR) Floor Hub
Dashboard / Manufacturing
Dashboard
Recent batches
Step-Level Master Formula Execution & CPP Interlocks
Batch execution
BCH-2026-0142 · Tablet Blend A
Electronic Line Clearance & Packaging Verification
Line clearance
Line 03 · Before BCH-2026-0142
Master Formula Record (MFR) Governance
Master Formula Record
MFR-TAB-A · Rev 03
Batch size
100 kg
Product
Tablet Blend A
Effective
01 Jun 2026
Quantify the financial impact of shifting from paper batch record reviews to Novaqis Dynamic eBR. Simulate reduction in QA review cycle times (14 days → 4 hours), liberated working capital, and elimination of investigation backlogs based on your plant's batch volume.
Capability depth
Novaqis BRM transforms pharmaceutical and biotech shop-floor operations into a dynamic, paperless execution engine. Master formula recipes, step-by-step electronic execution with dual 21 CFR Part 11 signatures, pre-flight cleanroom line clearance handshakes with Novaqis eLog™, and direct material issue integration with Novaqis ERP.
Manufacturing records
Manufacturing teams often run paper batch packs and chase documents, training, lab status, and holds in separate places. Novaqis BRM keeps electronic batch work on one clear record connected to the rest of the suite.
Paper packs, transcription, late reconciliation.
Recipes, execution, and completion on one record.
What to try in a pilot
+2 more evaluation items in the full comparison - expand above.
Separate print register, training sheets, hold emails.
Right documents, ready people, respected holds.
What to try in a pilot
+2 more evaluation items in the full comparison - expand above.
Lab and warehouse status chased by phone and spreadsheet.
Material context, lab disposition, equipment readiness.
What to try in a pilot
+2 more evaluation items in the full comparison - expand above.
Paper clearance and logbooks that lag the pack.
Clearance and logbooks with the batch story.
What to try in a pilot
+2 more evaluation items in the full comparison - expand above.
Categories describe common market patterns, not any specific vendor. Your process design and validation scope decide fit.
Regulatory alignment
Market Benchmarks
Technical Research
Talk to our team about how Novaqis BRM fits your validation and compliance requirements.
FAQ
