Hear the Almirall team explain how they achieved FMD compliance with TraceLink.
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Hear Central Pharma's Alwyn Smit talk about serialization's potential to revolutionize the industry.
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Get 27 answers covering the impact of validation to your requirements, resources, and risk—and how automation offloads the entire burden.
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From 9th February 2019, companies will need to comply with the EU FMD requirements for prescription medicines in Europe. Today marks 500 days until it comes into force.
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What would it mean for your Life Sciences supply chain business to enable serialization aggregation and support it? Understand the implications.
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Learn the language of wholesale distributor serialization to accelerate your compliance journey.
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TraceLink's network digitally connects the end-to-end pharmaceutical supply chain. See the infographic.
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See how experts have overcome roadblocks as they implement Level 1-5 solutions for EU FMD serialization.
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Hear wholesale distributor Burlington discuss how DSCSA lot level requirements have changed their business and how TraceLink has helped.
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Find out how many internal resources companies are dedicating to, and how much they're spending on track and trace system validation.
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Discover 4 key reasons Cheyenne Regional Medical Center chose a 3rd party solution to streamline their DSCSA compliance.
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Hear how addressing serialization well before your PDUFA date minimizes risk to your commercial launch.
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How can life sciences supply chain companies discover what’s going on in the industry? Hear about opportunities to network & share information.
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Review the different approaches healthcare organizations can take to achieve DSCSA compliance.
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To meet the DSCSA serialization deadline, pharmaceutical manufacturers must start preparing. Hear about compliance challenges.
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Learn the technical, legal, and industry terms you need to successfully prepare your company for EU FMD.
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Get insights into how much serialization will really cost your company. Proven serialization solution providers can help identify additional costs.
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With deadlines looming, hear how to determine if a serialization system has truly been tested, and what the consequences of an unproven solution might be.
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See why relying on your 3PL to build customizations to your existing systems isn't going to be enough to keep you compliant.
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Serialization aggregation has the potential to add both complexity and cost for life sciences supply chain businesses. Understand the basics
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See the most common misconceptions about DSCSA Saleable Returns Verification—and why wholesalers can’t afford to wait to implement a solution.
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View our infographic to find out how to comply with federal regulations for drug purity to stay DSCSA compliant now and down the road.
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Hospitals often ask what steps their peers are taking to ensure DSCSA compliance. Find out how five hospitals arrived at a plan.
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If you're a Phase 3 pharma company, serialization will be part of your strategy. Watch Sharp SVPs discuss how they approach serialization.
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Download this PDF to learn how an Edge solution can improve your operational efficiency.
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Learn from use cases that explore hub connectivity, onboarding & implementation timelines to meet compliance by February 2019.
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Get started with understanding EU FMD regulations and the serialization challenges ahead, with this introductory infographic guide.
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Pharma companies and CMOs must work together closely to be ready for serialization, yet there is no established commercial model. Learn about the dynamics.
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3PLs provide an essential service for pharma brand owners, not just in the U.S. and EU, but in other markets such as Korea, China and Brazil. Find out why.
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Leaving DSCSA details to TraceLink is a “no-brainer” for compliance-driven Crawford Memorial Hospital
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