Events, Webinars and Deadlines

Our calendar informs on industry events, upcoming compliance deadlines, as well as new Obelis webinars.

  • Swissdamed device registration becomes mandatory

    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. The deadline introduces new registration and compliance responsibilities for both manufacturers and their Swiss Authorised Representatives, making swissdamed registration an essential part of maintaining access…

  • Unlocking the UAE Cosmetics Market

    Virtual Event

    With the growing opportunities in the UAE cosmetics market, manufacturers and importers looking to expand into the region must understand and comply with local regulatory requirements to ensure successful market access. This expert-led session will provide a practical overview of the UAE cosmetics regulatory framework, covering key compliance obligations, product registration procedures, and the essential…

  • SupplySide Global Las Vegas

    Mandalay Bay Convention Center 3950 South Las Vegas Boulevard, Las Vegas, Nevada, United States

    Passionate about food supplements, nutrition and product innovation? Meet us at SupplySide Global this October! At Obelis Group, we help food supplement brands navigate regulatory requirements, achieve compliance and confidently expand into international markets. Why Meet Us at SupplySide Global? ✅ Expert guidance on food supplement compliance and market access✅ Tailored regulatory strategies for successful…

  • MEDICA 2026

    Dusseldorf, Germany Am Staad, Dusseldorf, Germany

    MEDICA is one of the world's largest B2B trade fairs for the medical industry, bringing together manufacturers, innovators and regulatory experts from across the globe. This year, Obelis will be there to help you navigate global market access with confidence. Whether you are planning to expand into new markets, launch a new medical device or…

  • EUDAMED Deadline

    Commission Decision (EU) 2025/2371 triggered the transition period leading to the 27 November 2026 deadline for the registration of legacy devices in EUDAMED. With the deadline approaching, manufacturers should ensure that the required device information is complete, accurate, and ready for registration. This involves more than entering data into EUDAMED: product and UDI information must…