Our calendar informs on industry events, upcoming compliance deadlines, as well as new Obelis webinars.
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…
The regulatory landscape for cosmetic fragrance ingredients is evolving rapidly, with new allergen disclosure requirements already in force and additional restrictions on the horizon. Is your business ready? Join our free webinar to gain a practical understanding of the latest EU regulatory developments affecting fragrance allergens and learn how they impact cosmetic formulations, labelling, and…
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? Join our free webinar to gain a practical understanding of the EU regulatory framework for food supplements and the key…
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…
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…