Deep Domain Knowledge
ZenoxLab's founder brings 12+ years of pharmaceutical IT experience. We understand GMP, GDP, the MHRA framework, and the operational reality of pharmaceutical warehousing, manufacturing, and distribution — not just the theory.
What We Build
Inventory & Warehouse Systems
FEFO/FIFO-enforced batch tracking, lot management, expiry monitoring, and warehouse location management. Systems that provide a complete, auditable chain of custody for every stock movement.
GRN & QC Workflows
Goods Receipt Note processes with QC hold management, vendor performance tracking, and promotional goods receipt. Configurable approval chains that match your SOP structure.
Audit Trails
Every data change is captured with timestamp, user identity, and before/after values. Designed for 21 CFR Part 11 and EU Annex 11 readiness — with tamper-evident storage and export capabilities.
GAMP 5 Alignment
We can support your GAMP 5 validation documentation — from IQ/OQ/PQ planning through to test evidence packages. Our development process is designed to generate the artefacts you need.
Why This Matters
A pharmaceutical system that fails an audit, causes a recall, or loses batch integrity data is not just a technical failure — it's a regulatory, commercial, and potentially patient-safety failure.
We design every system with that weight in mind.