Define systems and data flows
Digital logistics stays audit-ready only when master data, access, audit trails, interfaces and changes are controlled.
- URS, process and interface map
- WMS, ERP, scanners, loggers and FMD
Service area · GDP logistics
Validate WMS, ERP and logistics data for GDP and GxP use
tiger.PHARMA structures requirements, risks, tests and data controls for WMS, ERP, interfaces, monitoring and serialisation.
Discuss a pharmaceutical logistics project →WMS validation · GAMP 5 · ALCOA+ · audit trail
IT validation and data integrity in pharmaceutical logistics
tiger.PHARMA structures requirements, risks, tests and data controls for WMS, ERP, interfaces, monitoring and serialisation.
Digital logistics stays audit-ready only when master data, access, audit trails, interfaces and changes are controlled.
tiger.PHARMA Kompetenz
Topics we master
Plan risk-based validation
tiger.PHARMA translates product, quality, data and business requirements into an implementable target state and supports selection, qualification, migration, go-live and ongoing control.
- Risk assessment, test cases and traceability
- DQ/IQ/OQ/PQ or CSV evidence
Protect data integrity in operation
Metrics, deviations, changes and periodic reviews keep the process demonstrably effective.
- ALCOA+, roles, audit trail and backup
- Change control, periodic review and data quality
From requirements to stable operation
tiger.PHARMA translates product, quality, data and business requirements into an implementable target state and supports selection, qualification, migration, go-live and ongoing control.
- URS, RFI/RFP and decision model
- SOPs, quality agreement and responsibilities
- Pilot, acceptance, hypercare and KPI review
FAQ
Frequently asked questions
Does a WMS used in pharmaceutical logistics require validation?
Digital logistics stays audit-ready only when master data, access, audit trails, interfaces and changes are controlled.
How does tiger.PHARMA support implementation?
tiger.PHARMA structures requirements, selection, qualification, agreements, SOPs, tests, go-live and ongoing control. Scope depends on the product, authorisations, site and operating model.