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DTSTART;TZID=Europe/Brussels:20260701T000000
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UID:10000064-1782864000-1798761599@www.obelis.net
SUMMARY:Swissdamed device registration becomes mandatory
DESCRIPTION:From 1 July 2026\, manufacturers placing medical devices and IVDs on the Swiss market must ensure their devices are registered in swissdamed\, Switzerland’s national medical device database managed by Swissmedic. \n\n\n\nThe deadline introduces new registration and compliance responsibilities for both manufacturers and their Swiss Authorised Representatives\, making swissdamed registration an essential part of maintaining access to the Swiss market. \n\n\n\nEconomic operators have until 31 December 2026 to complete existing device registrations. However\, devices subject to vigilance reporting must be registered without delay and cannot benefit from this transition period. \n\n\n\nFor manufacturers established outside Switzerland\, registration is handled through their Swiss Authorised Representative (CH-REP). \n\n\n\nNeed support preparing for the swissdamed registration deadline? Whether you need a Swiss Authorised Representative (CH-REP) or assistance with device registration\, get in touch with us to ensure your devices remain compliant on the Swiss market.
URL:https://www.obelis.net/events/swissdamed-registration-deadline-2026/
CATEGORIES:Deadlines
ATTACH;FMTTYPE=image/jpeg:https://www.obelis.net/wp-content/uploads/2026/09/Deadline-swissdamed-1-1.jpg
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DTSTART;TZID=Europe/Brussels:20260923T150000
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DTSTAMP:20260907T134953Z
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UID:10000066-1790175600-1790179200@www.obelis.net
SUMMARY:Navigating EU Food Supplement Regulations: Claims\, Novel Foods & Market Compliance
DESCRIPTION:The EU regulatory landscape for food supplements can be complex\, with requirements varying depending on product classification\, ingredients\, claims and the Member State where a product is placed on the market. Is your business prepared? \n\n\n\nJoin our free webinar to gain a practical understanding of the EU regulatory framework for food supplements and the key requirements for compliant market access. Our experts will explain how food supplements are defined and differentiated from pharmaceutical products\, what is harmonised under the EU Food Supplements Directive and where national requirements still apply. \n\n\n\nThe session will also explore key compliance challenges surrounding health claims\, influencer marketing and Novel Food requirements\, including considerations for botanicals and other substances beyond vitamins and minerals. You will also discover how Obelis can support your compliance journey\, from FBO services and regulatory assessments to label and formula reviews and national notifications. \n\n\n\nWhether you are a manufacturer\, brand owner\, importer or regulatory professional\, this session will provide practical insights to help you better understand your obligations and confidently navigate the EU food supplement market.
URL:https://www.obelis.net/events/eu-food-supplement-regulations-webinar/
CATEGORIES:Webinars
ATTACH;FMTTYPE=image/jpeg:https://www.obelis.net/wp-content/uploads/2026/09/FS-Webinar.jpg
LOCATION:https://www.obelis.net/events/eu-food-supplement-regulations-webinar/
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