Register deviations, non-conformance, complaints, audit observations, line issues, and batch-related quality events.
All Meteor products
Pluggable CAPA product
Meteor CAPA
For QA teams tired of CAPA trackers, delayed approvals, and missing evidence.
"When CAPA and deviations are handled through Excel, emails, meetings, and paper files, ownership becomes unclear and evidence gets scattered. Meteor CAPA gives QA and manufacturing teams one controlled path from issue capture to investigation, action closure, and effectiveness verification."
What it helps you do
Guide risk assessment, root cause, corrective plans, approvals, and effectiveness checks.
Maintain a complete audit timeline for every CAPA decision.
Connect the work around Meteor CAPA
CAPA closureQMS routingAudit trailsDocument controleSign approvalsSOP acknowledgement
Before Meteor CAPA
CAPA work gets scattered.
- CAPA tracker in Excel
- Evidence in email or WhatsApp
- Approval delays and unclear owners
- Difficult audit reconstruction
- Effectiveness checks forgotten
After Meteor CAPA
One controlled CAPA timeline.
- Risk and RCA linked to the record
- Action owners visible
- Evidence attached in context
- Approval trail retained
- Effectiveness check tracked
IssueRisk assessmentInvestigationRoot causeCAPA planApprovalEffectiveness checkClosure
Meteor CAPA product overview
A controlled CAPA workspace with risk assessment, lifecycle progress, evidence, and approvals in context.
Risk-based CAPA
Tablet Dissolution Variance
CAPA-2026-0001 / linked issue ISSUE-2026-0001Add ActionRequest Approvals
CAPATablet Dissolution VarianceCAPA-2026-0001
Product / BatchGeneric Tablet BatchBT-2026-041
OwnerMeteor AdminQuality team
Due DateJun 23, 202628 days left
Progress11%Overall completion
CAPA Lifecycle
Controlled execution path1. ContainmentCompleted2. InvestigationPending3. Root CausePending4. Corrective ActionPending5. Preventive ActionPending6. VerificationPending7. MonitoringPending8. EffectivenessPending9. ClosurePending
Overview
Issue, product, source, and linked contextIssue SummaryTablet Dissolution VarianceCategoryProduct QualitySourceIn-Process TestSitePlant 01Reported ByMeteor AdminLinked IssueISSUE-2026-0001
Risk-based CAPA
Risk Assessment
Evaluate risk, impact, priority, and recurrence before CAPA execution.Create New Assessment
IssueTablet Dissolution VarianceRisk-based CAPA
CategoryProduct QualityProduct impact
Product / BatchGeneric Tablet / BT-2026-041Batch context
AssessmentCompletedRPN 80
Assessment Inputs
RPN = Severity x Occurrence x DetectabilitySeverity (S)Significant impact
Occurrence (O)Likely to occur
Detectability (D)Very low detectability
Risk Justification Material specifications do not meet purchase order requirements. If used in production, this could result in out-of-spec product quality. Immediate Impact Summary Stop the production of that batch.
What it does
Meteor CAPA gives every issue a controlled path to closure.
Moves events from issue capture to verified corrective action.
Keeps risk, ownership, approvals, evidence, and effectiveness in one path.
Helps pharma and manufacturing quality teams see what needs attention before it becomes noise.
How it works
1Issue
2Risk assessment
3Investigation
4Root cause
5CAPA plan
6Approval
7Effectiveness check
8Closure
Easy for users
Less chasing. More visible closure.
Avoid missed CAPA actions and reduce scattered evidence.
Track overdue actions, standardize closure, and maintain clear ownership.
Keep complete timeline history ready for audits and quality reviews.
Why pharma and manufacturing teams notice the difference
Why QA and manufacturing teams start with Meteor CAPA
The product is designed for everyday users first: clear tasks, visible state, controlled evidence, and enough structure for QA, plant, supplier quality, and manufacturing leaders to trust what happened.
Key features
From deviation intake to effectiveness verification, with evidence attached.
Register deviations, non-conformance, complaints, audit observations, line issues, and batch-related quality events.
Guide risk assessment, root cause, corrective plans, approvals, and effectiveness checks.
Maintain a complete audit timeline for every CAPA decision.
Avoid missed CAPA actions and reduce scattered evidence.
Track overdue actions, standardize closure, and maintain clear ownership.
Keep complete timeline history ready for audits and quality reviews.