Events, Webinars and Deadlines

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

  • EUDAMED Registration Becomes Mandatory – May 2026

    Regulatory Alert | EUDAMED becomes mandatory Commission Decision (EU) 2025/2371 confirms the full functionality of the first four EUDAMED modules. As a result, economic operators must comply with mandatory registration requirements. Mandatory modules from 28 May 2026: ✅Market Surveillance ✅Actors: registration of manufacturers, authorised representatives, importers ✅UDI / Devices: device registration (excluding custom-made devices) ✅Notified Bodies &…

  • EUDAMED Readiness for MDR & IVDR: Registration Obligations and Timelines

    With EUDAMED obligations becoming enforceable from 28 May 2026, manufacturers and economic operators should already be preparing for upcoming registration and compliance requirements under MDR & IVDR. During this expert-led session, our speakers will provide practical insights into the EUDAMED regulatory framework, key timelines and deadlines, affected economic operators, MDR & IVDR registration requirements including…

  • Webinar – Global Cosmetic Safety: Mastering Multiterritory Assessment & Laboratory Testing

    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…

  • EU & UK Detergents Market Access: Regulations & Upcoming EU Changes

    With evolving regulatory requirements shaping the detergents market in the EU and the UK, manufacturers and importers must ensure full compliance with applicable frameworks, registration obligations, and upcoming legislative changes. This expert-led session will provide a practical overview of the detergents regulatory landscape across both regions, including key compliance frameworks and requirements. The webinar will…

  • Cosmetic Claims Across Borders: Understanding EU and Turkish Requirements

    Join our webinar to gain practical insights into cosmetic claims and their growing importance in today's cosmetics industry. During this session, we will explore what constitutes a cosmetic claim, why claims have become a critical element of product development and marketing, and the regulatory expectations surrounding their use. Special attention will be given to “free…

  • 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…

  • Think You’re FDA Compliant? California May Require More

    Join our webinar to gain practical insights into the U.S. cosmetic regulatory landscape, with a focus on the relationship between federal requirements under MoCRA and California-specific compliance obligations. During this session, we will provide a brief overview of the Modernization of Cosmetics Regulation Act (MoCRA), including its scope and the distinction between federal and state-level…

  • Cosmoprof Las Vegas 2026

    Passionate about cosmetics and beauty innovation? Meet us at Cosmoprof Las Vegas this July! At Obelis Group, we help cosmetic brands simplify global regulatory compliance and confidently expand into international markets.Why Meet Us at Cosmoprof Las Vegas 2026?✅ Expert guidance on market access & compliance✅ Tailored regulatory strategies to support your market expansion goals ✅…

  • EU Fragrance Allergens Deadline

    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…

  • Cosmetic Allergens Regulation: New Requirements and Compliance Strategies

    Virtual Event

    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…

  • Navigating EU Food Supplement Regulations: Claims, Novel Foods & Market Compliance

    Virtual Event

    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…

  • 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…