<img src="https://secure.office-information-24.com/785669.png" style="display:none;">
Interactive concept mock • Illustrative data only • Not a live QT9 environment
Interactive DHR / EBR product story

See a Complete Digital Production Record Come Together.

Explore how QT9 can connect manufacturing data, quality evidence, traceability and approvals into an eDHR or EBR, then carry that record through controlled release and authorized review.

What do you manufacture?
Illustrative final state
Electronic Device History Record • MD-10482
100%Record complete
11Material lots linked
7Inspection results
✓ QA approved • Traceability available • Ready for authorized review
ProductionQualityReleaseAudit-ready access
Automatic record assemblyProduction and quality evidence connected
Forward + backward traceabilityMaterials through finished goods
Controlled QA releaseQuarantine, approval and disposition
Read-only auditor accessCompliance records without full ERP exposure
01 • Build the record

Build the record from connected evidence, not a post-production scavenger hunt.

Select the information sources manually or auto-connect them. The example record becomes more complete as manufacturing and quality evidence is linked.

Connected record sources

Choose single-level or multi-level record depth.
CONNECT INTO ONE CONTROLLED RECORD
0 of 6 sources connected
Illustrative record
Electronic Device History Record
Record ID
MD-10482
ProductSterile Infusion Set
StatusBuilding
RevisionRev. 07
Produced2,500 units
Released0 units
QA StatusAwaiting record
Record completeness0%
Start by connecting a source. Each source represents evidence that becomes part of the record.
02 • Traceability

Turn a traceability question into a visual answer.

Switch between forward and backward traceability to show how a material or finished lot connects to production records, components and distribution activity.

Choose a direction and run the trace.
The example will reveal the connected genealogy.
03 • Authorized review

Show an auditor what they need, not your entire ERP.

This compliance-facing concept demonstrates quick record retrieval, read-only access and separation from unrelated operational or financial information.

READ-ONLY AUDITOR
Device Lot MD-10482✓ Complete
Production Record
Material Traceability
Inspection Results
Controlled Documents
Electronic Approvals
Audit Trail
Financials remain hidden
Payroll remains hidden
Supplier pricing remains hidden
Concept message: authorized compliance information is quickly retrievable while unrelated ERP functions stay outside the auditor view.
04 • QA release

Connect record review, electronic approval and inventory disposition.

The release interaction illustrates separation of duties: manufacturing completes the work, quality reviews the evidence, and an authorized approver releases inventory.

1
Production Complete2,500 units
2
Quality ReviewInspections and documents verified
3
Electronic ApprovalSigner identity, time and meaning captured
4
Inventory ReleaseDisposition updates after approval
Quarantined
2,500 units awaiting QA dispositionProduction is complete, but inventory remains controlled.
PRE-RELEASE CHECK

Record readiness

Illustrative checklist for the selected record.
Production operations completeReady
Required inspections passedReady
Current controlled documents linkedReady
Material genealogy availableReady
Awaiting QA approval
The signature event will appear here after release.
05 • Master vs. actual

Connect what should happen to the evidence of what actually happened.

Click an approved control to highlight the corresponding execution evidence. This makes the relationship between the master and the production record tangible.

Approved Device Master / Production Standard

LINKS TO

Electronic Device History Record

06 • Before & after

From scattered evidence to one connected record.

The value story is not simply paper versus digital. It is fewer handoffs, less evidence hunting, and a clearer path from production completion to review.

Disconnected approach
Connected QT9 story
Find the traveler or batch packetLocate the execution history manually
Production data is already connectedExecution evidence is part of the record
Verify the approved revisionConfirm the correct master data and instructions
Approved revisions remain linkedMaster data and execution stay connected
Track down inspection resultsSearch separate quality records
Inspection results sit with the recordQuality evidence is available for review
Rebuild material genealogyTrace supplier and finished lots across systems
Forward and backward genealogy is searchableMaterials, jobs and finished goods stay linked
Collect signatures and assemble the packetPrepare the record after manufacturing
Review, sign and release through one workflowConnected evidence supports controlled disposition
One record storyProduction, quality, materials, documents and approvals
One traceability storyForward and backward genealogy for investigation or recall
One release storyQuarantine, QA review, signature and inventory status
Your walkthrough

See the complete story with your own process.

Your example is personalized for Medical Device manufacturing and a eDHR workflow.

MD-10482Single-level recordCurrent process: not selected
1
Record assembledConnect production and quality evidence
2
Lot tracedExplore forward or backward genealogy
3
Auditor record viewedSee a secure read-only experience
4
QA release completedApply a demonstration signature
Next step

Walk through this with your own manufacturing process.

See how QT9 could connect production, quality, traceability and compliance for your medical device, pharmaceutical or biotech operation.

Schedule a Call with a Life Sciences ERP Expert
Illustrative data only. Record IDs, quantities, people and workflow examples are for demonstration and do not represent a live QT9 environment.