Quality & deviations
Off-spec batches, deviations and CAPA handled in one place.
AI reads SDS and CoAs, spots recurring deviations and keeps raw materials planned. Make each batch to the approved formula, keep additions, process checks and lab results with it, and ship with the right certificate, label and lot trace.
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Five reasons not to put it off.
Paper hides addition errors.
A wrong charge or missing lab result stays buried until a customer rejects the load.
Add warehouse and quality when you're ready.
Raw material lots are logged with supplier CoA and the current SDS.
Only the approved formula revision is issued to the batch.
Each addition is scanned and weighed in sequence.
Lab results sit with the batch and feed the CoA.
Labels print from approved templates; drums trace to lots.
Each record stays linked by lot, for example SF-40218 → CH-2216 → Drums 2216-* → DSP-7730. People make the quality and release decisions; V5 keeps the evidence together. See inventory & traceability
It predicts and flags. Fixed rules decide. People sign.
Predicts demand before it hits.
Forecasts demand and tunes reorder points and safety stock for raw materials.
Quality, suppliers, equipment and customers alongside your formulas.
Off-spec batches, deviations and CAPA handled in one place.
Specifications, CoAs and current safety data sheets.
Vessels, scales and meters maintained and calibrated; OEE visible.
The approved formula, the right label and trained operators.



Approved formulas. Tested batches. Correct labels out the door.
36 pages · 4 worksheets · 15 primary sources
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We use your details to handle this request. Privacy policy. Practical orientation, not legal advice; your quality unit decides which rules apply.
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