Regulatory/Compliance
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EU FMD: 3 Key Compliance Challenges for Your Warehouse—and How to Solve Them
Learn three ways EU FMD will change your warehouse standard operating procedures.
An Overview of EU FMD
Understand the basics of EU FMD and what you need to do to comply by watching this 12-minute on-demand webinar with one of our experts.
Case Study: Medreich | EU FMD from Project Plan to Post Implementation
See how Medreich and TraceLink collaborated to achieve EU FMD compliance.
Ahead of the Curve: Wholesalers, Serialization, and Business Value
Learn more about wholesale distributors who have already begun to explore the potential value of serialized data.
Proven CMO Connectivity Prompts Pharma to Switch to TraceLink
Read why delayed development caused a European pharma to re-evaluate their choice of solutions provider for EU FMD compliance.
Company Switches to TraceLink After Two Unproven Providers Fail
Learn why a pharma company and CMO's first two choices failed to develop a successful EU FMD solution.
Case Study: Almirall | Best Practices for Falsified Medicine Compliance
Learn more about Almirall's organizational strategy for global serialization.
FDA Issues Long-Awaited Grandfathering Guidance
Insights into the November 27, 2017, FDA draft guidance around grandfathering product under DSCSA.
Russia Regulatory Updates
View a compilation of the most recent track and trace regulations for the healthcare supply chain in Russia. Get insights into compliance updates.
China Q&A: Preparing for New Reporting, Data, and Encoding Requirements
Learn how China’s National Medical Products Administration (NMPA) new reporting requirements and serialization options will affect pharmaceutical…
Faster Recalls, Better Visibility: How Serialized Inventory Can Transform Your Health System
Faster recalls and better visibility lead to improved patient care. Learn how the right approach to DSCSA compliance can do just that.
50 Must-Know Terms to Achieve EU FMD Compliance
Learn the technical, legal, and industry terms you need to successfully prepare your company for EU FMD.