June 11, 2020, 11 am CET
Parallel distributors and repackagers have unique obligations under the European Union Falsified Medicines Directive (EU FMD). They must take four steps to ensure compliance – from verifying medicines authenticity via the European Medicines Verification System (EMVS) and decommissioning the sourced products’ serial numbers, to serializing every repackaged medicinal product at the item-level and reporting the product data and new serial numbers to the verification system.
In this webinar, we will discuss how leveraging Movilitas.Cloud’s Repacker application can improve the entire repackaging process, while efficiently handling serialization requirements.These are the session’s key topics:
- Receiving process of sourced products
- Verification of sourced products
- Decommissioning towards the EU-Hub (check-out)
- Repackaging process (manual or automatic)
- Commissioning by Quality Assurance Manager
- Alert handling
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About Movilitas.Cloud
Movilitas.Cloud transforms the way products are serialized and verified while being easy to setup and use. Applications for pharma manufacturers (MAH and CMO), wholesalers, 3PLs (pre-wholesaler), parallel importers, repackagers and hospital pharmacies are tailored to the different legal requirements that these stakeholders need to fulfill, making compliance simple. Movilitas.Cloud is connected to the EU Hub and to all National Medicine Verification Systems in Europe and also easily integrates with partner systems such as SAP ATTP and SAP ICH.
Learn more: movilitas.com/expertise/movilitas-cloud
