Join TraceLink's Cloud Community to understand and overcome EU FMD compliance challenges.
View More
Prepare your hospital for EU FMD compliance by February 2019. Get the answers to your top 10 questions about EU FMD compliance.
View More
The EU Falsified Medicines Directive contains requirements for safety features and verification that details how companies must establish serialization and reporting.
View More
Learn three ways EU FMD will change your warehouse standard operating procedures.
View More
Read how a small pharma company discovered it could connect to all of its trade partners with one connection to TraceLink.
View More
Hear the IBERFAR team explain how they mastered serialization and FMD with TraceLink.
View More
As you begin to tackle regulatory compliance, you’ll hear references to the different “levels” of serialization. If you lack components at any level, your business is at risk.
View More
Read why a leading oncology-focused biotechnology company chose TraceLink's Automated Validation Manager (AVM) to reduce software validation complexity.
View More
Industry snapshot: Find out how digital transformation will lead to fewer drug shortages and better patient outcomes.
View MoreDiscover why this small French pharma company chose TraceLink for a cost-effective compliance solution.
View More
View a summary of the FDA's thoughts on the DSCSA verification requirements.
View MoreAs full FDA serialization enforcement begins on November 28, TraceLink has helped more than 250 manufacturing companies go live with serialization.
View MoreSee why companies should move ahead with a saleable returns solution even with FDA enforcement discretion.
View MoreCompanies that sell product into Russia need to focus on six critical considerations, and understand how Russia challenges differ from those of FMD and DSCSA.
View More
Watch this video to see why companies must be able to comply with regulations and operationalize global compliance solutions across diverse markets.
View More
Learn why a pharma company and CMO's first two choices failed to develop a successful EU FMD solution.
View More
Find out how hospitals and pharmacies can use edge data capture to improve both inventory management and patient outcomes.
View More
Stockpiling product to delay EU FMD compliance is a temporary approach that offers no long-term value—and carries significant risks.
View More
Read how McKesson is getting ready for the DSCSA saleable returns verification requirement, and how to handle DSCSA compliance in the face of it.
View More
Learn what issues one pharma company faced with other solution providers, and why it ultimately chose TraceLink for EU FMD compliance.
View More
Watch these brief videos to quickly understand how serialization compounds validation demands, and how to replace manual processes with automation.
View More
TraceLink SVP of Product Marketing, Lucy Deus, provides an in-depth review of the January 2019 Saudi reporting requirements for pharma supply chains.
View MoreNeeding to get control of spiraling infrastructure costs, one pharma switched to TraceLink for serialization. Find out more.
View More
Get expert advice on meeting Russia's complex track and trace requirements for pharmaceutical companies. Learn how TraceLink can help.
View More
One specialty packager believed their LMS vendor could handle their L4-L5 serialization. Find out what went wrong and why the CPO switched to TraceLink.
View More
Read the answers to 8 Russia compliance and cryptographic coding questions.
View More
Find out how TraceLink partnered with Savior Lifetec to serialize its product line and ultimately increase patient safety.
View More
Automated Validation Manager eases the burden of validation by testing functionality and providing a complete set of documents. Watch the video.
View More
Seven broken product recall practices across the end-to-end pharma supply chain—and five guiding principles for change.
View More
Faster recalls and better visibility lead to improved patient care. Learn how the right approach to DSCSA compliance can do just that.
View More