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…
For in vitro diagnostic (IVD) manufacturers navigating the transition to the In Vitro Diagnostic Regulation (IVDR), a key deadline is approaching. The IVDR legacy extension applies only if manufacturers meet specific requirements: Submission of an application to a Notified Body ✅ Class D devices (high-risk IVDs that were self-certified under IVDD but now require a…
Are Science and Beauty your work sectors? Then let's meet at NYSCC 2025, the premier event for personal care ingredients and formulations in North America! We are here to help your brand succeed in a globally regulated market.Why Meet Us at NYSCC?✅ Expert insights on market access & compliance✅ Tailored strategies to accelerate approvals✅ Guidance on…
Bringing Your Medical Devices to Market? Join us at FIME Miami, the largest international medical trade event in the USA!Our first goal? Supporting medical manufacturers in achieving regulatory compliance without the hassle. Why Meet Us at FIME? ✅ Expert insights on market access & compliance✅ Tailored strategies to accelerate approvals✅ Guidance on the latest regulatory…
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 at Cosmoprof Las Vegas, the leading B2B beauty exhibition in the USA! We can help your company decode and comply with global regulations with confidence.What will you get in return?✅ Expert insights on market access & compliance✅ Tailored strategies to accelerate approvals✅ Guidance on the latest regulatory updatesLet’s talk! Set up a meeting in…
Scientific Meetings and Clinical Lab Expo? Looking forward to it! Join us and the global laboratory medicine community at ADML Chicago. Question about compliance? No need to worry, we are here to help you!Why Meet Us at ADML?✅ Expert insights on market access & compliance✅ Tailored strategies to accelerate approvals✅ Guidance on the latest regulatory updatesSet…
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…
Heard about MEDICA? It is one of the largest medical B2B trade fairs in the world and we will be there to support you! Our goal is to assist your company in smoothly complying with global regulations. Why Meet Us at MEDICA? ✅ Expert insights on market access & compliance✅ Tailored strategies to accelerate approvals✅…
ISO 13485:2016 is the backbone of a compliant medical device business and a key enabler for CE marking and international registrations. In this webinar, we’ll go beyond the basics and show, in practical terms, who ISO 13485 applies to, how it links with EU MDR/IVDR and ISO 9001, and how it supports market access.Through clear…
Switzerland - Effective Date of Furocoumarin Restriction ✅1 January 2026: In finished cosmetic products, excluding perfumes, eaux de toilette and eau de cologne, the sum of the concentrations of the furocoumarins Byakangelicol, Epoxy-bergamottin, Isopimpinellin, 5-Methoxypsoralen, 8-Methoxypsoralen, Oxypeucedanin, Oxypeucedanin hydrate and Psoralen must be present in quantities below 1 mg/kg, and natural essential oils must be dosed accordingly, where, under…
France - PFAS prohibition effective date ✅01 January 2026: New prohibition for making available on the market products containing intentionally added PFAS The 01 January 2026 PFAS ban is approaching, and timely compliance is key to keeping your products on the market without interruption. Obelis is here to provide expert guidance and practical support, ensuring you meet the…
United Kingdom - Benzophenone‑3 & Methyl Salicylate Restrictions Deadlines ✅21 January 2026: Cosmetic products containing Benzophenone-3 and not complying with the restrictions outlined in Annex VI can no longer be placed on Great Britain’s market. For full details on the restrictions, please refer to this link. ✅31 March 2026: Cosmetic products containing Methyl Salicylate (CAS 119-36-8)and not complying with the…
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…
Heading to WHX Dubai 2026? It's one of the most dynamic stages for international business growth and Obelis Group is excited to be part of it! At Obelis, we help companies navigate complex medical devices and IVDs regulatory landscapes so they can enter markets with confidence and speed. What You Can Expect When You Meet…
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…
A New Milestone in Cosmetics Compliance & Safety In 2026, the European Cosmetics Responsible Person Association (ERPA) Annual Conference - formerly known as the CRCC - enters a new chapter. With a new name, an expanded agenda, and a sharpened purpose, the event reflects the evolving needs of the cosmetics regulatory community. Now reintroduced as…
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…
Heading to Cosmoprof Bologna?One of the leading global events for the beauty and cosmetics industry, Cosmoprof Bologna is a key platform for international growth and Obelis Group is pleased to be part of it. At Obelis, we support companies in navigating complex cosmetics regulatory landscapes, enabling confident and efficient access to global markets. What you…