Our calendar informs on industry events, upcoming compliance deadlines, as well as new Obelis webinars.
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…
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,…
Canada - Fragrance Allergen Disclosure Deadline ✅12 April 2026: New and existing cosmetics have to disclose the 24 fragrance allergens listed below within the list of ingredients, when present at concentration greater than 0.01% in rinse-off products and 0.001% in leave-on products. To ensure compliance with the above regulatory changes, we recommend reviewing and, where…
Making plans to attend Interclean Amsterdam? This April, the world’s leading cleaning and hygiene event returns to the RAI Amsterdam with an expanded show floor and more international exhibitors. Interclean Amsterdam is the premier stage for the professional cleaning industry and Obelis Group is proud to be part of the movement. At Obelis, we help…
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,…
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…
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…
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…
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,…
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…
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…
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 &…
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…
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…
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…