LabsVerified proof

Every inspection-ready story, packaged for your board and regulators.

The LabsVerified evidence program collects telemetry, outcomes, and audit narratives from global laboratories so your stakeholders see tangible, defensible impact in weeks—not quarters.

CAP 21st Ed.CLIA 493ISO 15189GDPRHIPAA
Evidence briefing highlights
Access anonymized materials from enterprise deployments with structured walkthroughs.

Live walkthrough

45-minute review with quality strategists covering program scope and ROI.

Evidence vault

Audit-ready binders, SOP rollouts, and KPI dashboards safe-shared under NDA.

Benchmark canvas

Peer comparisons spanning deviation velocity, regulator response, and attestation.

Proof points that withstand inspection

These metrics originate from third-party validated reports and documented change management overseen by LabsVerified strategists.

1.4M

QC events reconciled

Validated against LIS and middleware feeds across 37 countries in the last 12 months.

68%

Deviation velocity gain

Median reduction in investigation-to-closure time across enterprise deployments.

24 hrs

Regulator response

Average turnaround for supplying auditable narratives to CAP, CLIA, ISO, and local inspectors.

98%

User attestation

Supervisors and medical directors reporting sustained confidence in QC signal integrity.

Case studies curated for your stakeholders

Dive into anonymized playbooks detailing program structure, outcome metrics, and regulator correspondence for peer laboratory networks.

Integrated delivery network
Meridian Health Network
Unified nine laboratories, harmonized QC SOPs, and eliminated spreadsheet-based audit prep with LabsVerified as the system of record.

73%

Deviation cycle time reduction

$820K

Annual labor savings

End-to-end adoption playbook and inspector sign-off letter.

Reference lab & vendor consortium
Nova Diagnostics
Connected vendors to live QC telemetry, driving collaborative corrective actions and verifiable SLA adherence across 64 sites.

4x

Faster vendor resolution

100%

Shared audit readiness

Vendor governance model with reconciled event playbacks.

Multi-country molecular network
TransLab Europe
Scaled ISO 15189 accreditation with localized evidence packs, automated document attestation, and multilingual SOP releases.

+14

Markets onboarded in phase one

0

Regulatory non-conformances

Validation dossier and regulator correspondence tracker.

Validation journey, mapped week by week

Your LabsVerified strategist orchestrates a predictable rollout so operations, quality, and compliance teams align on milestones and evidence outputs.

  1. Week 0

    Evidence intake

    Joint workshop aligns data sources, compliance goals, and success metrics before we import historical QC backlogs.

    Deliverables

    Scope brief, data validation plan, chain-of-custody matrix

  2. Week 3

    Signal activation

    Live telemetry normalizes instrumentation feeds, while deviation copilots begin recommending corrective actions with owner routing.

    Deliverables

    QC normalization report, deviation automation blueprint

  3. Week 6

    Audit rehearsal

    Teams rehearse regulator scenarios using generated narratives, evidence binders, and SOP attestations kept in LabsVerified.

    Deliverables

    Inspector briefing deck, audit pack preview, SOP attestation log

  4. Week 10

    Executive validation

    Quality and compliance leadership receive outcome dashboards, ROI modeling, and peer benchmarks ready for board review.

    Deliverables

    Board-ready scorecard, ROI analysis, peer benchmark digest

Regulatory frameworks supplied
Each pack is aligned to mandated standards and localized obligations.

CAP 21st Edition

Narratives mapped to phase 0–3 checklists with automated deficiency back-fill workflows.

Automated binder generation
Corrective action traceability
Proficiency event reconciliation

CLIA 493

Live dashboards convert QC telemetry into compliance attestations by laboratory specialty.

Method performance trending
Personnel competency tracking
Deviation signature trails

ISO 15189

Localized templates and multilingual SOPs align to country-specific accreditation supplements.

Document lifecycle controls
Risk register with mitigation status
Partner audit collaboration

GDPR & HIPAA

Evidence packs ship with data processing agreements and access proofs satisfying dual jurisdiction requirements.

Access receipts
Data minimization attestations
Encryption compliance log
Validation FAQ
Compliance and quality leaders typically ask these before enrolling in our briefing program.

Customer commentary

Direct quotes captured during validation reviews and subsequent renewal cycles.

LabsVerified gives my leadership team real-time QC telemetry without chasing email threads. Our ISO audits are now narrative-driven and effortless.

LC

Dr. Lina Chen

Chief Laboratory Officer, Aurora Clinics

The vendor co-pilot changed how we collaborate. Turnaround on escalations dropped from days to hours once everything lived in one playbook.

MR

Miguel Rodríguez

Director of Quality Systems, Vida Diagnostics

Evidence packs that once took weeks are ready in minutes. Every inspector we host now sees the same verified source of truth across our sites.

ST

Sophie Tremblay

Regional Compliance Lead, NorthRiver Labs

Ready when you are

Bring platform evidence to your next executive review

Book your validation briefing to receive the anonymized evidence pack, ROI model, and regulator-ready narratives tailored to your network.