Regulatory/Compliance
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DSCSA 2023: How Does the FDA Define “Suspect Product”?
Learn how recent FDA guidance provides more detailed definitions to help dispensers identify a suspect product.
DSCSA 2023: 3 Key Requirements for Pharmacies and Health Systems
Learn why retail pharmacies and health systems need to implement new solutions to meet DSCSA 2023 interoperability requirements for compliance with…
DSCSA 2023 for Health Systems and Pharmacies: 50 Essential Terms
These 50 terms will help pharmacies and health systems understand important DSCSA concepts as they prepare for the 2023 deadline.
DSCSA Governance Group Reveals 2023 Interoperability Blueprint
See why the Partnership for DSCSA Governance Blueprint is the “starting gun” for meeting DSCSA 2023 requirements.
United Kingdom Regulatory Updates
View a compilation of the most recent track and trace regulations for the healthcare supply chain in The United Kingdom.
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.
Understanding Russia Compliance Complexities and Preparation Timeline
View this on-demand webinar to understand complex Russia compliance regulations and deadlines.
Case Study: Mithra | Serializing Across Multiple Business Cases
Learn how Mithra used a multidisciplinary approach for a successful EU FMD go-live.
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.
EU FMD: The Risks of Product Stockpiling
Stockpiling product to delay EU FMD compliance is a temporary approach that offers no long-term value—and carries significant risks.
Validation and Automated Validation: Top Industry Questions
Get 27 answers covering the impact of validation to your requirements, resources, and risk—and how automation offloads the entire burden.