Recipes & products
- Master formulas with clear revision history
- Scale and material planning from the approved recipe
- A starting point inspectors can follow
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Batch execution & embedded ERP operations
Paper batch binders and late reconciliations delay release and heighten 483 audit risks. Novaqis BRM combines step-level digital recipe execution, built-in ERP material management (dispensing, weighing scale integration, yield mass balance), and electronic logbooks with automated Review-by-Exception for rapid batch disposition.
Dashboard / Manufacturing
Dashboard
Recent batches
At a glance
Why Novaqis BRM
The points below map to real architecture and delivery choices—not generic marketing bullets.
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.
Verify raw material lots via barcode scanning, integrate weighing scales directly for tare/net calculations, reserve inventory lots, and automate theoretical vs actual yield mass balance tracking.
Seamlessly sync batch production orders, material consumptions, and Usage Decisions (UD) directly with SAP S/4HANA or third-party ERP platforms without manual transcription.
Automated QA dashboard aggregates analytical results, critical process parameter limits, and deviation flags, compressing final batch disposition from 3 days to under 2 hours.
Pre-batch line clearance checklists and digital room/equipment logbooks with verified corrections, ensuring 100% audit-ready contemporaneous floor evidence.
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.
Core BRM capabilities
Recipes, execution, clearance, and floor logbooks on one clear record, connected to controlled documents, operator readiness, lab disposition, and quality holds so the plant and QA share one story.
EBR
Electronic batch lifecycle
MFR
Master formula records
DMS
Issuance interlock
LMS
Qualification gate
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
Talk to our team about how Novaqis BRM fits your validation and compliance requirements.