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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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  • Notified Bodies for IVD (EU vs CANADA)

    Navigating the EU In Vitro Diagnostic Regulation (IVDR) and Health Canada requirements can be challenging. Understanding the role of Notified Bodies and regulatory expectations is crucial for compliance and market access. Our exclusive webinar will cover: ✅Strategies for efficient regulatory compliance in both regions ✅Key differences between EU IVDR and Health Canada requirements ✅The role of Notified Bodies and how they impact IVD approvals 🎯 When: March 18th | 16:00-17:00 CET…

  • EUDAMED & National Registration: Navigating Compliance for Medical Devices

    Join our webinar to get the inside scoop on EUDAMED compliance and make the process easier for your company. We'll break down what data is public in EUDAMED and explain how it affects your business. You’ll learn how to correctly assign and use EMDN codes and stay on track with important EUDAMED deadlines to keep your operations running smoothly, and much…

  • GPSR, VAT Compliance, and Customs: Essential Insights for Market Entry

    Handling EU regulations can be challenging, but our expert-led webinar will give you the insights you need to stay compliant and efficient. Learn about VAT obligations, EPR rules across countries, customs clearance, post-Brexit shipping considerations, and GPSR product requirements. Don’t miss this opportunity to equip yourself with the knowledge to expand confidently! Here’s what you…

  • FDA U.S. Agent and Submissions

    Join us for this essential webinar. Whether you're preparing your first submission or trying to keep up with evolving requirements, we’ve got the insights to help you move forward with certainty.Webinar highlights include: ✅Cybersecurity  ✅U.S. Agent and Official Correspondent ✅Establishment Registration and Device Listing ✅Submissions (GUDID, 510k and others) 🎯 When: May 8 | 16:30-17:30 CET 📌 Where: Online…

  • GB/UK Post Market Surveillance: What You Need to Know

    Navigating the evolving regulatory landscape in the UK can be complex, especially when it comes to Post Market Surveillance (PMS). Join us for this essential webinar as we break down the latest updates and practical requirements of the UK PMS (Amendment) (Great Britain) Regulations 2024. Whether you're a medical device manufacturer, a UK Responsible Person,…

  • EUDAMED & Swissdamed Explained: Key Modules and Timelines for Medical Devices

    Join us for an insightful webinar on EUDAMED and Swissdamed, where we’ll explore the key modules, important timelines, and compliance requirements for medical devices. Webinar highlights include: ✅What is public? ✅Code Usage ✅Timelines ✅Client Experiences to date 🎯 When: September 9 | 16:00-17:00 CET 📌 Where: Online | Zoho Webinars  🎬 Guests: Richard Houlihan (EirMed) and Georgios Mariolos (Obelis Group)

  • Navigating Canadian Ingredient Approval and the EU/UK Split

    Cosmetic regulations are evolving quickly, are you keeping up?  Join our interactive session where we will explore the Canadian, EU and UK frameworks using real-life examples to show you exactly how these rules can affect your business and impact your compliance journey. After this session, you will walk away with practical tips to navigate ingredient…

  • EU vs Turkish Cosmetics Regulations: Key Differences and Compliance Pathways

    Join our webinar on EU vs. Turkish Cosmetics Regulations to understand the key differences in cosmetics notification systems, Responsible Person (RP) obligations, and labeling requirements. Whether you plan to register cosmetics in Türkiye or maintain EU compliance, this session will give you expert guidance on regulatory submissions, packaging compliance, and market access strategies; helping you…

  • EUDAMED, Swissdamed & IVDR Legacy: What You Need to Know

    Join us for an in-depth live webinar where we explore the latest developments in EUDAMED, the European database for medical devices. This session will provide a clear overview of the key EUDAMED modules, implementation timelines, and how they impact manufacturers and stakeholders. We will also cover Swissdamed, highlighting Switzerland’s alignment with European regulations, and discuss…

  • How 2026 Bans & Cosmetic Rules Will Impact Your Business?

    2026 will be a turning point for the cosmetics industry. With new bans, PFAS restrictions, allergens labelling rules, and tightened compliance deadlines across major markets, brands that don't adapt quickly may face delays, reformulations, blocked products, or market loss.  Join our LIVE session where we'll break down the most important 2026 regulatory shifts and show…

  • Powering Compliance: EU Battery Regulation for Portable Batteries

    Join us for an insightful webinar on EU battery regulation, with a focus on portable batteries. We will cover an overview of the EU Battery Regulation, highlight the main novelties, and explore key provisions specific to portable batteries. Gain practical guidance, understand compliance requirements, and learn how to navigate the evolving regulatory landscape effectively.🎯 When: March 12…

  • Navigating U.S. FDA Medical Device Regulations: Pathways & Lifecycle Compliance

    Entering the U.S. medical device market requires a clear understanding of FDA regulatory requirements throughout the entire product lifecycle. This webinar will guide you through the key elements manufacturers must consider when placing a device on the U.S. market and maintaining compliance over time.Our experts will cover essential topics including:✅Device classification✅Regulatory pathways (510(k), De Novo,…

  • 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…

  • 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,…

  • 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…

  • Banner image for a webinar on EU & UK detergents market access regulations, highlighting upcoming EU regulatory changes affecting detergents, chemicals compliance, labeling, sustainability, and product market entry requirements.

    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…

  • 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…

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