THIS WEBINAR ENDED. YOU CAN ACCESS THE RECORDING BELOW.
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EMVO Onboarding & EU Falsified Medicines Directive:
What to Know and Where to Begin
Presented by:
Fanny Trenteseaux Project Coordinator/Customer Relation Manager
European Medicines Verification Organisation &
Mark Davison Senior Operations Director for rfxcel
Please join us for a webinar explaining the EMVO Onboarding Process and the Falsified Medicines Directive requirements; co-presented by Fanny Trenteseaux of the European Medicines Verification Organisation (EMVO) and Mark Davison of rfxcel. On this hour-long call, we will provide:
- A brief introduction to the EU Falsified Medicines Directive/Delegated Regulation
- Explanation of the EMVO and how to onboard your organization
- How to choose a gateway provider (IT partner)
- Q&A – plenty of time to get your specific queries answered
About Our Speakers:
Fanny Trenteseaux, a member of EMVO’s Commercial & Partner Management team, is a Project Coordinator and Customer Relation, Manager. She is actively assisting with the contractual on-boarding process, manages the Legitimacy Check process, and manages the Community of National Medicines Verification Organisations.
Mark Davison, Senior Operations Director for Europe at rfxcel, is a leading traceability and digital health 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.
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