Pharmaceuticals
Powering Pharmaceutical Precision
Datex Footprint® WMS gives pharmaceutical manufacturers the control, compliance, and visibility to manage raw materials, intermediates, packaging, and finished goods with total accuracy.
From batch release to cold-chain distribution, our platform helps you maintain GxP and cGMP compliance while keeping your supply chain moving at full speed.
Maintaining Control Beyond Production
In pharmaceutical manufacturing, a warehouse is more than storage—it’s an extension of the production line. Each vial, blister pack, and shipment must move under strict control with total transparency and complete documentation.
Footprint WMS helps pharmaceutical suppliers uphold Good Automated Manufacturing Practice and Good Manufacturing Practice (GxP/cGMP) standards and Drug Supply Chain Security Act (DSCSA) standards, ensuring products are safely released, tracked, and delivered with confidence.
GxP & cGMP Compliance
Maintain validated, audit-ready workflows for regulated materials and finished goods.
Serialization & DSCSA Traceability
Capture, aggregate, and report GTIN, lot, and serial data for full supply chain visibility.
Environmental Monitoring
Track temperature and humidity across storage zones to ensure product stability and integrity.
Quality Hold & Release Control
Enforce quarantine, quality review, and release workflows to verify each batch before it moves to distribution.
David Hamilton
Vice President of cGMP Warehousing, Tobin Scientific
With GMP operations, traceability is everything—being able to see every signature and step in the process. We had a third party validate the system and had zero observations during the audit. It went smoother than expected for a new system, which really shows how strong it is from a compliance standpoint.
Engineered For The Science of Pharmaceutical Logistics
Footprint WMS gives pharmaceutical manufacturers the visibility and validation tools to meet regulatory expectations while improving operational efficiency. From production staging to finished-goods fulfillment, it ensures every batch is documented, traceable, and audit-ready.
Stay Inspection-Ready Every Day
- Validated GxP and cGMP workflows with audit trails
- Secure electronic signatures and controlled document versioning
- Quality assurance hold and deviation management for every batch
Protect Product Integrity and Compliance
- Serialization aggregation and reporting to meet DSCSA requirements
- Continuous temperature and humidity monitoring across all storage zones
- Complete chain-of-custody tracking from production through distribution
Integrate the Pharmaceutical Supply Chain
- Connect seamlessly with MES, ERP, and serialization systems
- Sync data with QA, LIMS and regulatory reporting platforms
- Manage multi-site operations within one validated, centralized WMS