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SFL to present on supply chain and EU regulation at the MPP2020 virtual conference

SFL’s Head of Supply Chain Barbara Polek is presenting at the Medtech & Pharma Platform Virtual Annual Conference (22-23 October 2020, online). Barbara’s presentation “Promoting patient safety through new supply chain controls under the Medical Device Regulation (MDR) and the Falsified Medicines Directive (FMD)” will be on October 23, 11:00 am CEST (Session 5 on Patient/user needs in development of combined products). Barbara is an expert in supply chains for pharmaceutical and medical device products, and her talk will be of particular significance considering the increased supply during the current pandemic of products from new sources of difficult-to-verify quality, and compliance with relevant regulations. Barbara will also be part of the session’s discussion panel alongside an expert patient speaker, and a human factors and usability design expert, where participants can provide their perspectives and have their questions answered.

SFL has extensive experience and expertise in supply chain for medical devices and pharma products. SFL supports clients to establish a seamless supply chain for new products, as well as streamline or expand existing supply chains in compliance with existing and new regulations. Discover SFL’s supply chain services that can provide tailored solutions; from ensuring your products meet identification and authentication requirements, to supporting market entry, early access, distribution and master data management. Contact us to arrange a meeting with Barbara to discuss how SFL can support in optimizing the supply of your products.

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SFL Regulatory Affairs & Scientific Communication GmbH
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Email: office@sfl-services.com
Phone: +41 61 361 9443

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