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 & production records
Paper packs and late reconciliation slow release and fray nerves before inspection. Novaqis BRM keeps recipes, execution, clearance, and floor logbooks on one clear record—connected to the documents and training your plant already trusts.
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 master formulas with clear revision history—the starting point for initiation and scale, not a printed binder that drifts.
From start through execution and completion, with signatures where your policy needs them—and a path to investigate when materials or yields demand it.
Keep material context with the run so release is not a hunt across inventory spreadsheets and chat threads.
Bring lab disposition into the release decision—so certificates and status are part of the story, not a side conversation.
Check that instruments are fit before critical steps—so calibration surprises do not arrive with the auditor.
Clear the line before execution and keep the evidence with the batch for QA and inspection readiness.
Floor logbooks with sign, verify, and proper corrections—same discipline as the batch record, without the binder.
Confirm controlled-copy context before work begins, and keep execution evidence tied back to the document story.
Operator readiness from training can matter before a manufacturing step runs—competency is not a spreadsheet taped near the line.
When quality places a hold, release can wait until it is cleared—manufacturing and QA decide together.
One login and licensing model with Admin, DMS, LMS, and QMS—manufacturing records that belong in the same validation story.
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.