3PLs will need to upgrade their WMS or go with a solution like TraceLink to support serialization. Find out the other two components 3PLs need.
View MoreLearn why TraceLink is the experienced partner you can rely on for Russia compliance.
View MoreWatch this brief webinar excerpt to learn how Patheon by Thermo Fisher Scientific is facilitating true partnership with its suppliers to improve quality processes and achieve real results.
View MoreWith the DSCSA serialization deadline looming, get a bird’s eye view into the life of a serial number as it travels through the pharmaceutical supply chain.
View MoreWatch our webinar as 3M, Patheon, Reed-Lane, Sharp and Teva share best practices to help brands and CMOs accelerate their progress to November 2017.
View MoreUnderstand the basics of EU FMD and what you need to do to comply by watching this 12-minute on-demand webinar with one of our experts.
View MoreGet insight into the state of EU FMD readiness for 100+ pharma companies and CMOs.
View MoreView this on-demand webinar to understand complex Russia compliance regulations and deadlines.
View MoreIn this on-demand webinar, TraceLink experts field saleable returns and enforcement discretion questions and discuss why companies need to move forward.
View MoreSee how 331 life sciences companies are faring with DSCSA lot-level requirements and serialization readiness.
View MoreView this on-demand webinar on saleable returns, DSCSA requirements and the role of master data.
View MoreView this on-demand webinar to see why your VRS solution capabilities should include performance, security, and interoperability.
View MoreEasily share master data with your trading partners and enable DSCSA saleable returns verification with TraceLink's digital sharing platform.
View MoreLearn how Tjoapack turned the challenge of updating packaging for EU FMD into an opportunity for innovation, in this on-demand webinar.
View MoreRecorded at the 2020 LogiPharma Digital Summit, this panel of industry leaders and academic experts explores the necessity of building more agile pharmaceutical supply chains. Hosted by TraceLink’s Chief Digitalization Officer, Roddy Martin.
View MoreAggregation has the potential to add more complexity and cost to serialization, which already poses significant challenges to the life sciences supply chain.
View MoreLearn what you need to build your strategy for serialization and compliance.
View MoreIf you haven’t started receiving transaction documentation (T3) in electronic format, your paperwork could be throwing you out of compliance.
View MoreDownload our guide for CMOs to learn how to adapt your operations to meet your customers’ EU FMD requirements.
View MoreSwiss pharma company Actelion and Allpack, a contract packager, discuss how they worked together towards serialization.
View MoreLearn more about Almirall's organizational strategy for global serialization.
View MoreHear the Almirall team explain how they achieved FMD compliance with TraceLink.
View MoreHear Central Pharma's Alwyn Smit talk about serialization's potential to revolutionize the industry.
View MoreGet 27 answers covering the impact of validation to your requirements, resources, and risk—and how automation offloads the entire burden.
View MoreFrom 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.
View MoreWhat would it mean for your Life Sciences supply chain business to enable serialization aggregation and support it? Understand the implications.
View MoreLearn the language of wholesale distributor serialization to accelerate your compliance journey.
View MoreTraceLink's network digitally connects the end-to-end pharmaceutical supply chain. See the infographic.
View MoreSee how experts have overcome roadblocks as they implement Level 1-5 solutions for EU FMD serialization.
View MoreHear wholesale distributor Burlington discuss how DSCSA lot level requirements have changed their business and how TraceLink has helped.
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