Our calendar informs on industry events, upcoming compliance deadlines, as well as new Obelis webinars.
Join us for an expert-led session on navigating cosmetic safety in a complex global regulatory landscape. As cosmetic products cross borders, ensuring compliance is no longer a one-time task, it requires a strategic, science-driven approach that integrates multiterritory safety assessment, robust laboratory testing, and continuously updated documentation. In this webinar, we will explore how laboratory…
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…
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…