Our Products

Purpose-Built Applications for
Life Science Excellence

Five deeply integrated enterprise applications sharing one data model — giving your team unified visibility across quality, training, documents, lab, and people.

QMS

Quality Management System

Stay inspection-ready every day. Voyantix QMS automates CAPA workflows, deviation tracking, and change control with a complete audit trail aligned to ICH Q10 and FDA guidance — so quality events are captured, routed, and closed without manual chasing.

  • CAPA Management with intelligent routing and escalation
  • Deviation Tracking with root cause analysis tools
  • Change Control with cross-functional impact assessment
  • Risk Assessment aligned with ICH Q9 methodology
40%Faster CAPA closure through automated workflows and escalations
0483 observations by design — full audit trail from day one
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Quality Management Lifecycle
ICH Q10 COMPLIANT
CAPA
Root cause analysis
Deviation
Event tracking
Change Control
Impact assessment
Audit
Inspection readiness
Risk Assessment
ICH Q9 aligned
FDA
21 CFR Pt.11
ICH Q10
PQS Aligned
ISO 9001
Principles
LMS

Learning Management System

An undertrained employee is a compliance risk. Voyantix LMS automatically assigns role-based curricula, tracks competency assessments, and captures electronic signatures per 21 CFR Part 11 — so every training record is complete and instantly retrievable for any FDA or EMA inspection.

  • GxP Training Tracking with automated due-date management
  • Curriculum Management with role-based assignment rules
  • Competency Assessment with pass/fail thresholds
  • Training Matrix with live compliance gap detection
80%Reduction in training coordination administrative time
100%Training record completeness — every record audit-ready, always
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GxP Training Journey
Assign
Role curriculum
Learn
GxP modules
Assess
Competency test
e-Sign
21 CFR Pt. 11
Certify
Audit-ready record
Training Matrix — Role Compliance
Manufacturing
100%
QC Laboratory
94%
Quality Assurance
98%
Electronic Signatures Automated Assignment Complete Audit Trail
DMS

Document Management System

Every SOP, protocol, and policy must travel from draft to archive with complete traceability. Voyantix DMS automates the full document lifecycle with native 21 CFR Part 11 e-signatures and automatic version control — so no one ever works from an obsolete procedure again.

  • Controlled Document Lifecycle from draft to archive
  • Version Control with automatic obsolescence management
  • Electronic Approval Workflows with parallel and sequential routing
  • Complete Audit Trail on every document interaction
65%Reduction in document approval cycle time
ZeroObsolete documents accessed since DMS deployment
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Controlled Document Lifecycle
SOP
Policy
Protocol
Work Instr.
Document Lifecycle
Draft
Review
Approve
Distribute
Archive
21 CFR Part 11 Compliant
Every document action recorded with e-signature and immutable audit trail
LIMS

Laboratory Information Management System

From sample receipt to Certificate of Analysis, Voyantix LIMS tracks every step with chain-of-custody, e-signatures, and immutable audit trails. Direct instrument integration eliminates manual transcription errors and our OOS/OOT module guides analysts through compliant investigation workflows.

  • Sample Management with full chain-of-custody tracking
  • Instrument Integration for direct data capture
  • Certificate of Analysis (CoA) generation with e-signatures
  • OOS/OOT Investigation workflows per FDA guidance
15hrsPer week saved through direct instrument integration (vs. manual re-entry)
10minTo produce a full lab audit report vs. 2+ days of manual effort
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Sample-to-Release Workflow
Sample
Receipt
›
Sample
Preparation
›
Analysis &
Testing
›
Results
Review
›
CoA
Release
Direct Instrument Integration
HPLC / GC Systems
Analytical Balances
Environmental Monitors
Spectrophotometers
Chain of Custody OOS/OOT Workflows 21 CFR Part 211
HRMS

Human Resource Management System

In life sciences, HR is inseparable from compliance. Voyantix HRMS manages GxP-qualified workforces from the ground up — when an employee's role changes, training curricula update automatically and CAPA actions follow them through any organizational change.

  • Employee Records with complete qualification history
  • Role-Based Training Assignment linked to LMS curricula
  • GxP Qualification Tracking with expiry management
  • Onboarding Workflows with automated task assignment
100%Onboarding completion tracked and auditable from day one
ZeroQualification gaps — real-time compliance tracking for every role and employee
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GxP Workforce Management
Organisation — 247 Employees
Mfg
100%
68 staff
QC Lab
97%
42 staff
QA
100%
31 staff
R&D
89%
28 staff
Role-Based Qualification Tracking
Sarah Mitchell — QC Analyst II
GMP · HPLC · Aseptic · 21 CFR Pt.11
Qualified
Anika Sharma — QA Specialist
ICH Q10 · Audit · SOP — Training Due
Action Needed
Integrated with:
LMS QMS
Platform Architecture

All Products. One Platform. One Data Model.

Every Voyantix application shares a unified data layer. A training record in LMS automatically satisfies a CAPA requirement in QMS. A lab deviation in LIMS triggers a quality event in QMS. Your people data in HRMS drives curriculum assignments in LMS. No integrations to build. No data silos.

Voyantix
Platform
QMS
LMS
DMS
LIMS
HRMS
SAP / Oracle ERP
Instrument Systems
Cloud Storage
REST API
Transparent Pricing

Get Pricing for Your Organization

Voyantix pricing is based on your organization size, modules selected, and deployment model. Get a personalized quote and product demo tailored to your specific use case.

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