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…
Starting on 31 July 2026, cosmetic products placed on the EU market must comply with the updated labelling requirements, including the disclosure of 56 additional fragrance allergens where applicable. From this date onwards: ✅ Products that do not meet the updated labelling requirements may be held at customs, refused entry, or removed from the market…