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eQMS / eDMS / LIMS

Purpose-built, GxP-compliant software for life science organisations — validated, audit-trailed and inspection-ready from day one.

eQMS · eDMS · WMS · LIMS 21 CFR Part 11 Annex 11
Overview

Digital Quality Systems, Delivered Validation-Ready

Buying GxP software is easy. Proving it is validated, controlled and inspection-defensible is where most implementations stall. We deliver our platforms with the validation package, so the system arrives with its IQ, OQ and PQ evidence rather than a promise to produce it later.

Every product below enforces audit trails, electronic signatures and role-based access as standard — not as a paid add-on.

At a Glance

  • eQMS with full audit trail and e-signatures
  • eDMS controlled document lifecycle
  • WMS and LIMS for GDP and GLP

Need this scoped for your facility and target market? A senior consultant will give you a candid read at no cost.

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Our Software Products

Four platforms covering quality, documents, warehouse and laboratory.

eQMS

Electronic Quality Management System

An audit-trail-enabled platform covering deviations, CAPAs, change control, document management, training records and complaints in one workflow engine.

21 CFR Part 11Annex 11Audit Traile-Signatures
eDMS

Electronic Document Management System

Controlled document lifecycle with version control, review and approval workflows, distribution tracking and compliant archiving.

Version ControlWorkflowsAccess ControlGxP Validated
WMS

Warehouse Management System

GDP-compliant inventory control with quarantine management, FIFO/FEFO enforcement and temperature monitoring integration.

GDP CompliantTraceabilityTemperature Log
LIMS

Laboratory Information Management System

Sample management, test scheduling, results capture, OOS/OOT handling and stability study management.

GLP/GMPOOS/OOTStabilityInstrument Interface

What Ships With Every Implementation

The validation package is part of the deliverable.

  • User requirement specification — Written against your process, not a generic template.
  • IQ, OQ and PQ protocols — Executed and reported, with traceability matrix back to the URS.
  • Role-based access control — Segregation of duties enforced and documented for inspection.
  • Data migration validation — Verified transfer of legacy records with reconciliation evidence.
Next Step

Ready to Transform Your GxP Strategy?

Book a no-obligation consultation and get practical answers about eqms, edms, wms & lims software for your specific product, facility and target market.