Global Track & Trace
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What are the Language Requirements for EU FMD Safety Features?
Discover what language the new unique identifier needs to be in on your medicine packs, depending on which European market you ship to.
Case Study: Nestlé Skin Health | Benefits of Aggregation as a Standard
Learn how Nestlé Skin Health uses Edge Track to support their aggregation goals.
Rising to the Challenge of Russia Compliance: An Interview with Santen Pharmaceutical’s Pasi Kemppainen
Learn how Santen Pharmaceutical is navigating Russia's highly complex and demanding serialization and track and trace regulations.
IBERFAR: Partnering with TraceLink for FMD and Digital Integration
Hear the IBERFAR team explain how they mastered serialization and FMD with TraceLink.
Case Study: Almirall | Best Practices for Falsified Medicine Compliance
Learn more about Almirall's organizational strategy for global serialization.
What's So Challenging about Continuous Compliance?
In the new regulatory landscape, maintaining compliance is a real challenge.
Brazil Compliance and Serialization Terms
Brazil track and trace regulations are entering implementation phase. Learn key terms for Brazil regulation and serialization. Download the PDF.
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.
Leading India Pharma Co. Gains Edge in Operational Efficiency, Compliance
Download this PDF to learn how an Edge solution can improve your operational efficiency.
European Contract Packager Tjoapack Paves the Way for Supply Chain Efficiency
Read about contract packager Tjoapack's readiness to meet EU FMD deadlines and provide customers with an easy path to compliance.
India Regulatory Updates
View a compilation of the most recent track and trace regulations for the healthcare supply chain in India. 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…