Regulatory/Compliance

Hear the IBERFAR team explain how they mastered serialization and FMD with TraceLink.

View this on-demand webinar to understand complex Russia compliance regulations and deadlines.

Learn how Mithra used a multidisciplinary approach for a successful EU FMD go-live.

Brazil track and trace regulations are entering implementation phase. Learn key terms for Brazil regulation and serialization. Download the PDF.

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

Get 27 answers covering the impact of validation to your requirements, resources, and risk—and how automation offloads the entire burden.

Read an interview with ACS PharmaProtect to learn how the German national system works and how it will operate under EU FMD.

In this webinar series, TraceLink experts will guide you through the maze of saleable returns and product verification:

Learn how China’s amended Drug Administration Law expands the scope of NMPA reporting requirements and impacts your company’s serialization strategy.

What does the EU FMD mean for hospitals, pharmacies, and dispensing doctors? Get insights into the basics of EU FMD.

See the most common misconceptions about DSCSA Saleable Returns Verification—and why wholesalers can’t afford to wait to implement a solution.

If your business is aggregating, you need to know how to upload your product data once EU FMD comes into effect. Find out here.