{"listFuture":[{"invisible":false,"invisibleInfo":null,"parentExh":null,"id":"activity=0q9T6ikDQOG2VSWNOHk7tg","title":"Spotlight sessions with BSI Experts","text":"<p>Choosing a Notified Body is one of the most consequential decisions a manufacturer makes. It shapes your timelines, your market access, and your ability to plan with confidence. Experience can help bring greater clarity to a complex regulatory process. Access to reviewers with relevant technical expertise can support more focused discussions and help you better understand what to expect throughout the conformity assessment process.&#160;</p><p><br></p><p>As a leading full scope Notified Body under the Medical Device Regulation (MDR) and the In Vitro Diagnostic Regulation (IVDR), BSI reviews devices across every risk class and technology area – from software as a medical device and active implantables to companion diagnostics and combination products.</p><p><br></p><p>We will be hosting a series of Spotlight Sessions at our booth, delivered by members of our technical team, covering key topics in the industry.</p><p><br></p><p>If you and your colleagues are interested in attending these sessions, please take a look at the agenda and register using the link below. Registration is completely free: Agenda - MEDICA 2026: Spotlight Sessions with BSI Experts </p>","type":"activity","date":"2026-11-17T00:00:00Z","dateUntil":null,"isMeeting":false,"wholeday":true,"image":"https://www.medica.de/vis-content/event-medica2026/exh-medica2026.3073286/MEDICA-2026-BSI-Group-Image-medica2026.3073286-ySjPmvMSRjK1TQABjvirAA-image.jpg","imageText":null,"imageTitle":"MEDICA_INVITE_1200x800px_FINAL","link":null,"location":"Hall 10 / F52"},{"invisible":false,"invisibleInfo":null,"parentExh":null,"id":"activity=7oAoc7kxRRq2tQodMiSMmg","title":"Spotlight Sessions with BSI Experts","text":"<p>Choosing a Notified Body is one of the most consequential decisions a manufacturer makes. It shapes your timelines, your market access, and your ability to plan with confidence. Experience can help bring greater clarity to a complex regulatory process. Access to reviewers with relevant technical expertise can support more focused discussions and help you better understand what to expect throughout the conformity assessment process.&#160;</p><p><br></p><p>As a leading full scope Notified Body under the Medical Device Regulation (MDR) and the In Vitro Diagnostic Regulation (IVDR), BSI reviews devices across every risk class and technology area – from software as a medical device and active implantables to companion diagnostics and combination products.</p><p><br></p><p>We will be hosting a series of Spotlight Sessions at our booth, delivered by members of our technical team, covering key topics in the industry.</p><p><br></p><p>If you and your colleagues are interested in attending these sessions, please take a look at the agenda and register using the link below. Registration is completely free: Home - MEDICA 2026: Spotlight Sessions with BSI Experts </p>","type":"activity","date":"2026-11-18T00:00:00Z","dateUntil":null,"isMeeting":false,"wholeday":true,"image":"https://www.medica.de/vis-content/event-medica2026/exh-medica2026.3073286/MEDICA-2026-BSI-Group-Image-medica2026.3073286-Oveqr4NKRHuXXjFkhUDbOg-image.jpg","imageText":null,"imageTitle":"MEDICA_INVITE_1200x800px_FINAL","link":null,"location":"Hall 10 / F52"}],"listPast":[]}