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…
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 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…
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…