Global Track & Trace
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EU FMD: The Risks of Product Stockpiling
Stockpiling product to delay EU FMD compliance is a temporary approach that offers no long-term value—and carries significant risks.
McKesson Q&A: The Challenge of Saleable Returns Verification
Read how McKesson is getting ready for the DSCSA saleable returns verification requirement, and how to handle DSCSA compliance in the face of it.
French Pharma Selects TraceLink for Smooth LMS Integration, Lower Costs
Learn what issues one pharma company faced with other solution providers, and why it ultimately chose TraceLink for EU FMD compliance.
Automating Validation with Every Release
Watch these brief videos to quickly understand how serialization compounds validation demands, and how to replace manual processes with automation.
Preparing for Saudi Arabia Compliance Reporting
TraceLink SVP of Product Marketing, Lucy Deus, provides an in-depth review of the January 2019 Saudi reporting requirements for pharma supply chains.
Delivery Issues and High TCO Prompt Generics Pharma to Switch to TraceLink
Needing to get control of spiraling infrastructure costs, one pharma switched to TraceLink for serialization. Find out more.
From Crypto Codes to Complex Reports: Expert Advice on TraceLink’s Russia Compliance Solution
Get expert advice on meeting Russia's complex track and trace requirements for pharmaceutical companies. Learn how TraceLink can help.
CPO Switches to TraceLink After Costly Integration Effort Fails
One specialty packager believed their LMS vendor could handle their L4-L5 serialization. Find out what went wrong and why the CPO switched to…
Russia Compliance and Crypto Coding: Top 8 Questions Answered
Read the answers to 8 Russia compliance and cryptographic coding questions.
Savior Lifetec: Serialization-Ready on TraceLink’s Network
Find out how TraceLink partnered with Savior Lifetec to serialize its product line and ultimately increase patient safety.
Automated Validation Manager: How It Works, and What's Included
Automated Validation Manager eases the burden of validation by testing functionality and providing a complete set of documents. Watch the video.
Fixing Recalls: FDA Pilot Tackles a Legacy Challenge—7 Broken Practices and 5 Guiding Principles for Change
Seven broken product recall practices across the end-to-end pharma supply chain—and five guiding principles for change.