Learn about the key features of TraceLink Automated Validation Manager, the key to ensuring continuous validation across the lifecycle of your TraceLink solutions.
View MoreWill you be ready? Pharmacies are starting to recognize the potential business value of the data in the 2D barcode and data matrix. Read to see why.
View MoreShipment delayed due to serialization exceptions? Learn how TraceLink can help.
View MoreAvoid supply chain disruptions and take your serialized operations from reactive to proactive with Serialized Product Intelligence. Watch the demo.
View MoreRead why delayed development caused a European pharma to re-evaluate their choice of solutions provider for EU FMD compliance.
View MoreLearn how TraceLink can help you boost the efficiency of serialized operations.
View MoreWhat is Serialized Product Intelligence? TraceLink's Bharath Sundararaman explains in these quick videos.
View MoreWatch TraceLink's Brian Daleidan talk about the challenges companies face in meeting Brazil's regulatory and business requirements for supply chains.
View MoreWatch this video to see Brian Daleiden talk about changes to Brazil compliance timelines and why companies must still plan to meet the 2022 deadline.
View MoreBrazil track and trace regulations are entering implementation phase. Learn key terms for Brazil regulation and serialization. Download the PDF.
View MorePharmaceutical companies cannot afford to delay their Brazil planning and preparation if they are going to meet the proposed December 2020 ANVISA deadline.
View MoreIntegration with ANVISA's reporting system, SNCM, will be a critical focus for both domestic and multinational manufacturers in 2020.
View MoreIn this video, TraceLink experts explain why Brazil may be your biggest compliance challenge.
View MoreSuccess in the Brazilian market will depend on horizontal integration: end-to-end data exchange between you and your trading partners. Learn why.
View MoreWatch this video to learn how TraceLink’s integrated pharma supply chain platform can give you inventory visibility across your global markets.
View MoreSee the latest regulatory developments in the Gulf Cooperation Council, Indonesia, Malaysia, and Africa from TraceLink’s Brian Daleiden.
View MoreTraceLink Director of Industry Marketing, Brian Daleiden, discusses how Saudi Arabia fits into a global compliance strategy for pharma supply chains.
View MoreLearn how TraceLink enables Orient Pharma to deliver serialization at a global scale.
View MoreLearn about the updated process for being approved to send data to the EU Hub.
View MoreManual data upload through the EMVO portal is simple in concept, but preparing and maintaining that data can be a challenge for smaller companies.
View MoreThe 2019 China Drug Administration Law introduced track and trace terms and agencies that you need to understand for your China compliance strategy.
View MoreChina eCode or GS1 Encoding: Which one is right for you? Watch this short webinar excerpt to understand key considerations for your China product strategy.
View MoreWhat makes China compliance so challenging? Watch this brief overview of China’s 3-tier reporting system to help guide your China serialization strategy.
View MoreLearn how China’s National Medical Products Administration (NMPA) new reporting requirements and serialization options will affect pharmaceutical companies.
View MoreChina's drug administration law and serialization framework for medicines could affect your China product packaging strategy. Learn how today.
View MoreReview the different approaches healthcare organizations can take to achieve DSCSA compliance.
View MoreTo meet the DSCSA serialization deadline, pharmaceutical manufacturers must start preparing. Hear about compliance challenges.
View MoreLearn the technical, legal, and industry terms you need to successfully prepare your company for EU FMD.
View MoreGet insights into how much serialization will really cost your company. Proven serialization solution providers can help identify additional costs.
View MoreWith 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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