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The EU Falsified Medicines Directive – for the Pharmaceutical Dispenser

THIS WEBINAR ENDED. YOU CAN ACCESS THE RECORDING BELOW.

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SEP 26, 2018

Please join rfxcel for a webinar that will provide insight into the upcoming serialisation requirements of the EU FMD and how this relates specifically to Dispensers. In this 45 minute presentation, we will discuss:

1. Overview of the key features of the FMD
2. What the FMD means for Dispensers: Who does what and when are they expected to do so
3. What to think about when selecting a FMD solution provider
4. Stand alone FMD solution versus those integrated with pharmacy software – Pros and Cons
5. How installation and roll-out is performed

About our Speaker:

Mark Davison, based out of the UK, is a leading traceability and digital heath expert as well as the published author of “Pharmaceutical Anti-Counterfeiting: Combating the Real Danger from Fake Drugs”. Mark specializes in global health and big data issues such as serialisation, supply chain security, patient safety and government policy. Mark is currently the Senior Operations Director for Europe, at rfxcel, and is looking forward to the opportunity to share his expansive knowledge on this topic.

PLEASE FILL OUT FORM TO ACCESS WEBINAR RECORDING: