Lab Relations
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QMS Software
for Life Science Teams

  • ✓ eQMS purpose-built for life science
  • ✓ ISO 13485, 21 CFR Part 820, cGMP, and 15+ standards
  • ✓ Go live in weeks with guided onboarding
Regulatory grade quality stars
LabRelations QMS Software for Life Sciences

Why life science teams choose LabRelations QMS

One quality system.
Built for life science compliance.

Manage documents, deviations, changes, training, risk, and supplier records in a system designed for GxP environments. Stop chasing spreadsheets and shared drives. Know your compliance posture at all times.

  • Replace fragmented tools with one controlled environment.
  • Enforce approval workflows, review cycles, and training requirements.
  • Maintain complete audit trails across all quality processes.
  • Scale from a single site to multi-location quality programs.

Built for the way life science teams work

Document control
without the overhead

Author, review, approve, and distribute SOPs, policies, and work instructions in structured workflows. Every document version is tracked, every approval recorded. Employees read and acknowledge the right revision automatically.

  • Approval workflows with electronic signatures
  • Automatic version control and revision history
  • Periodic review scheduling and escalation
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Document control in LabRelations QMS

Deviations & change control

Capture deviations the moment they occur. Investigate root causes, assess impact, and route changes through structured approval. Link corrective actions to the deviation that triggered them, so nothing falls through the cracks.

  • Deviation capture with classification and risk grading
  • Change requests with impact assessment and approval routing
  • Linked CAPA actions tracked to verified closure
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Deviation and change control management

Training management
tied to your documents

When an SOP changes, training assignments update automatically. Track who has been trained, who is overdue, and which roles require which competencies. Generate training matrices for auditors in seconds.

  • Auto-assignment when documents are revised
  • Role-based training curricula and competency tracking
  • Training effectiveness records and re-qualification scheduling
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Training management tied to documents

Risk & supplier management

Identify, assess, and mitigate risks with structured registers and scoring. Qualify and monitor suppliers against your quality requirements. Keep risk assessments and supplier records linked to the processes they affect.

  • Risk registers with likelihood, severity, and detectability scoring
  • Supplier qualification workflows and periodic re-evaluation
  • Traceability from risk controls to SOPs and training records
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Risk and supplier management

Built for the standards you follow

Medical Devices

  • ISO 13485 (Quality management systems)
  • ISO 14971 (Risk management)
  • 21 CFR Part 820 (Quality System Regulation)
  • EU MDR (2017/745)
  • IEC 62304 (Software lifecycle)

Pharmaceutical & Biotech

  • 21 CFR Part 210/211 (cGMP)
  • ICH Q10 (Pharmaceutical quality system)
  • EU GMP Annex 11 (Computerised systems)
  • EU GMP Annex 15 (Qualification and validation)
  • GAMP 5 (Compliant GxP systems)

Cross-functional Life Science

  • 21 CFR Part 11 (Electronic records & signatures)
  • ICH Q9 (Quality risk management)
  • ICH Q12 (Lifecycle management)
  • EU GxP (Good practice guidelines)
  • ISO 14971 (Risk management for medical devices)

Purpose-built for your industry

Medical Devices

  • Design history file and DHF traceability
  • Risk management per ISO 14971
  • Post-market surveillance records
  • Supplier qualification for components
  • EU MDR and 510(k) documentation support
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Pharma & Biotech

  • GxP-compliant document control
  • Batch record deviation tracking
  • Validation lifecycle management
  • Change control for methods and processes
  • Supplier and vendor qualification
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Contract Testing Labs

  • SOP management tied to lab methods
  • Multi-client quality record separation
  • Instrument qualification and calibration
  • OOS/OOT investigation workflows
  • Audit readiness for client inspections
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A life science eQMS

Purpose-built for pharma, biotech, and medical devices. Not a generic QMS adapted to your industry.

Reliable support

Practical support from quality systems specialists.

Go live in weeks, not months

Guided onboarding and migration from day one.

Available from anywhere

Access quality records, approvals, and training status from any location.

Data owned by you

Customer-owned records with controlled access and full auditability.

Fully configurable

Tailor workflows, forms, approval chains, and permissions to your processes.

Take part in the LabRelations community

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Do you want to try
our QMS for free?

  • Purpose-built for life science compliance
  • Document control, deviations, CAPA, and training
  • Go live in weeks, not months
  • Always audit-ready. Zero scramble.
Yes, I want a free trial account

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