Is Your Supply Chain Software Ready for New Regulations?
Regulatory changes are reshaping pharma and medical device supply chains—from DSCSA enforcement to FDA Precheck and evolving AI guidelines. Outdated or fragmented systems could put compliance and operations at risk. To stay ahead, your WMS needs:
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Full Product Traceability
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Audit-Ready Reporting
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Validated, Compliant Systems
End-to-End Traceability
Tryon Solutions ensures your WMS tracks lot numbers, serial numbers, and expiration dates in real time, helping you meet DSCSA and FDA requirements while reducing the risk of recalls or compliance gaps.
Regulatory Reporting & Audit Readiness
We build dashboards and reporting workflows that unify data, speed decision-making, and make FDA, EU, and global regulatory audits straightforward and accurate.
WMS Validation & System Integrity
Our team manages WMS validation, documenting processes, implementing change controls, and preforms testing so your system stays compliant and GxP-ready.
SaaS Migration & System Optimization
We guide SaaS transitions, clean up legacy configurations, and optimize system performance to create a scalable, stable, and regulation-ready WMS environment that supports ongoing compliance.
Modern WMS for Pharma & Medical Device Companies
Meeting today’s regulatory demands requires more than standard warehouse management. Systems must enable traceability, accurate reporting, and validated processes to reduce compliance risk and keep operations running smoothly.
Tryon Solutions helps companies upgrade their WMS, streamline workflows, and maintain regulatory alignment, so your supply chain stays efficient, compliant, and audit ready.