Available to explore in demonstrations.
An existing demonstration shows this part of the workflow. The label does not mean a live service is ready for your facility.
Capabilities & status
The full scope. A clear view of its state.
Start with the job your team needs to do. Then check the maturity label. A screen preview, an implemented foundation and a planned capability are different things.
Read the labels before the features
Taking shape in development.
Part of the record structure or workflow exists. Further development and validation are needed before the capability is complete.
Planned for the full system.
Part of the intended product direction, not an available feature or a commitment to a delivery date.
Start with the task your team needs to complete. A workflow review can clarify which capability—and which development state—matters to that task.
CONTROL
Define what good work requires.
Controlled documents and specifications
Find the procedure version, owner and approval context behind an operational record.
Structured HACCP and preventive-control plans
Link hazard analysis, preventive controls, critical limits and monitoring requirements. Qualified people approve the plan.
Product, allergen and label control
Carry specifications, allergen requirements, artwork and change impact into the operating record.
Confirmed product scope; no implementation evidence supplied for this extension.OPERATE
Record the work where it happens.
Daily checks and operational records
Keep production, receiving, sanitation and pre-operation observations tied to their source and responsible role.
Schedules and expected records
Define which checks should exist and identify missing or late records against that expectation.
Supplier documents and shipment dossiers
For applicable Trade workflows, connect supplier records, certificates of analysis and shipment documentation.
Optional Trade extension · Applicability first
Production, rework and transformation
Extend batch records to quantities, inputs, outputs, rework, waste and relevant process checks.
Confirmed product scope; no implementation evidence supplied for this extension.DETECT
Make the exception visible.
Exceptions and limit comparisons
Compare an observation with a defined limit and preserve the source of the exception for review.
Complaints and cross-domain quality events
Use the same event model for complaints, supplier issues, environmental findings and other exceptions.
Confirmed product scope; no implementation evidence supplied for this extension.INVESTIGATE
Test a cause against the facts.
Investigation and incident analysis
Bring 5 Why, cause-and-effect diagrams and 8D problem solving into the event history.
Recurrence and trend investigation
Use historical findings and source-linked patterns to examine recurring problems without treating correlation as a cause.
Confirmed product scope; no implementation evidence supplied for this extension.ACT
Give the next action an owner.
CAPA, holds and product disposition
Assign corrective and preventive action, required evidence and verification. Authorized people make product decisions.
Controlled change and effectiveness
Review change impact, follow implementation and check effectiveness before authorized closure.
Confirmed product scope; no implementation evidence supplied for this extension.TRACE
Follow the affected product.
Supplier, lot, batch and shipment links
Follow the relationships between received materials, transformations, finished lots and shipments.
Mock recall, withdrawal and recovery
Use the trace foundation to scope affected product, track response steps and prepare reviewable recall records.
Confirmed product scope; no implementation evidence supplied for this extension.ASSURE
Verify that the control holds.
Training, calibration and maintenance
Bring competency and equipment checks into the context of the work being reviewed.
Import–export control plane
Keep relevant external references, broker exchanges and cross-border document controls alongside the quality trail.
Optional Trade extension · Applicability first
Supplier quality programmes
Extend supplier records into approval, risk review, incoming defects, certificate review and performance follow-up.
Confirmed product scope; no implementation evidence supplied for this extension.Sanitation, environmental monitoring and cold chain
Review the checks and findings that establish whether operational controls remain effective.
Confirmed product scope; no implementation evidence supplied for this extension.Standards and requirement-to-evidence mapping
Map applicable requirements to controls, records, gaps and actions. Support preparation, not certification guarantees.
Confirmed product scope; no implementation evidence supplied for this extension.PROVE
Show the full basis of the decision.
Reports and audit packages
Prepare scoped evidence packages and management-review records that lead back to the sources.
Management review and source-linked reporting
Explore trends, recurring costs and performance with a route back to the underlying records.
Confirmed product scope; no implementation evidence supplied for this extension.AI-assisted review and preparation
Support summaries, drafts, pattern review and missing-evidence checks across the chain. Human approval remains separate.
Confirmed product scope; no implementation evidence supplied for this extension.Use the status labels to distinguish demonstrations from developing and planned workflows. Discuss availability and fit for your operation during a workflow review.
Standards preparation
Map the requirement.
Show the supporting record.
The intended standards workflow links applicable requirements to controls, records, gaps and corrective action. Scope may include SQF, BRCGS Food Safety, FSSC 22000 or ISO 22000 where relevant to an operation.
These names describe potential mapping context. They are not certifications held by Zentria, partnerships or guarantees of audit outcomes.
VISION · REQUIREMENT-TO-EVIDENCE MAPPINGA practical place to start
Bring one workflow.
Find the missing links.
A recurring exception. A difficult handoff. An audit trail that takes too long to reconstruct. Start with the work your team already knows.
Request a workflow reviewFirst, check your workflow