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Events, Webinars and Deadlines

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

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  • The Critical Role of the Responsible Technical Person

    2026 is a critical year for cosmetic compliance - and the Responsible Technical Person is at the center of it.Join our 60-minute LIVE webinar to discover how to safeguard your products, avoid regulatory risks, and implement GMP with ISO 22716. ✅ GMP Essentials: key principles for cosmetic products✅ RTP Responsibilities: legal and operational must-knows✅ Practical Tips: ensure compliance efficiently✅ Expert Insights: from Sandra Ferretti, CCO at Obelis Group, and Selim Erol,…

  • ON-DEMAND WEBINAR: Food Supplements in the EU and UK – a focus on online sales (AMAZON)

    Get a clear and practical overview of the essential rules governing food supplements in the EU and UK. This on-demand webinar walks you through the core legislation and compliance requirements every Food Business Operator (FBO) must know.Webinar highlights :✅ Regulation (EC) 178/2002 – General Food Law✅ Brexit and its impact on labeling & notifications✅ Compliance challenges when selling…

  • Omnibus Act VIII – May 2026

    European Union - Omnibus Act VIII amends the Cosmetic Regulations ✅1 May 2026: Products containing 3-(4′-methylbenzylidene)-camphor  (CAS No 36861-47-9/38102-62-4) can no longer be made available on the market. ✅1 May 2026: With no distinction between placing products on the market and making them available, Omnibus Act VIII will apply. This means that, from the application date, non-compliant cosmetics can…

  • GITEX Future Health Africa

    Heading to GITEX Future Health Africa?As Africa’s leading platform for health innovation and policy, GITEX Future Health Africa is where healthcare’s evolution meets the continent's digital future. Obelis Group is more than excited to be a part of this transformative event in Morocco this May. In an era where AI and deep tech are reimagining…

  • Winning with IVDR: Compliance Strategy, Class C Pathways & NB Engagement

    The IVDR transition is reshaping how IVD manufacturers approach compliance, evidence, and certification. This session will guide you through the most critical elements of the journey, from transition timelines and legacy provisions, to EUDAMED and UDI requirements, and what they mean in practice. We will also dive into Class C classification and conformity assessment pathways,…

  • Beauty Istanbul 2026

    Keen on Beauty Care? Let's meet at Beauty Istanbul, one of the largest cosmetics exhibitions worldwide! Our Mission? Helping cosmetics brands seamlessly adapt to global compliance standards.Why Meet Us at Beauty Istanbul?✅ Expert insights on market access & compliance✅ Tailored strategies to accelerate approvals✅ Guidance on the latest regulatory updatesLet’s connect to discuss how we can…

  • IVDR Class C Transitional Deadline – May 2026

    As the transition to the In Vitro Diagnostic Regulation (IVDR) continues, we would like to remind you of the critical 2026 deadlines for legacy IVDs that are classified to Class C under IVDR. For these devices, the following milestones apply:  ✅A written agreement between the manufacturer and the Notified Body must be signed by 26 September 2026. ✅The manufacturer or their Authorised…

  • 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 &…

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