Regulatory/Compliance

Learn why a pharma company and CMO's first two choices failed to develop a successful EU FMD solution.

Find out how hospitals and pharmacies can use edge data capture to improve both inventory management and patient outcomes.

Stockpiling product to delay EU FMD compliance is a temporary approach that offers no long-term value—and carries significant risks.

Read how McKesson is getting ready for the DSCSA saleable returns verification requirement, and how to handle DSCSA compliance in the face of it.

Learn what issues one pharma company faced with other solution providers, and why it ultimately chose TraceLink for EU FMD compliance.

Watch these brief videos to quickly understand how serialization compounds validation demands, and how to replace manual processes with automation.

TraceLink SVP of Product Marketing, Lucy Deus, provides an in-depth review of the January 2019 Saudi reporting requirements for pharma supply chains.

Get expert advice on meeting Russia's complex track and trace requirements for pharmaceutical companies. Learn how TraceLink can help.

Read the answers to 8 Russia compliance and cryptographic coding questions.

Automated Validation Manager eases the burden of validation by testing functionality and providing a complete set of documents. Watch the video.

Seven broken product recall practices across the end-to-end pharma supply chain—and five guiding principles for change.

Faster recalls and better visibility lead to improved patient care. Learn how the right approach to DSCSA compliance can do just that.