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