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DTSTART;TZID=Europe/Brussels:20260326T160000
DTEND;TZID=Europe/Brussels:20260326T170000
DTSTAMP:20260407T131944
CREATED:20260317T080848Z
LAST-MODIFIED:20260323T131642Z
UID:10000042-1774540800-1774544400@www.obelis.net
SUMMARY:Navigating U.S. FDA Medical Device Regulations: Pathways & Lifecycle Compliance
DESCRIPTION: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\, and PMA)✅Labelling requirements✅Post-market surveillance obligations✅UDI implementation✅Implications of the FDA’s new Quality Management System Regulation (QMSR)Join us to gain practical insights into navigating the FDA regulatory framework and ensuring your medical devices remain compliant from market entry through post-market monitoring.
URL:https://www.obelis.net/events/fda-medical-device-regulations-us-market-pathways-lifecycle-compliance/
CATEGORIES:Webinars
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END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Brussels:20260326T090000
DTEND;TZID=Europe/Brussels:20260328T180000
DTSTAMP:20260407T131944
CREATED:20260107T145612Z
LAST-MODIFIED:20260108T083727Z
UID:10000027-1774515600-1774720800@www.obelis.net
SUMMARY:Cosmoprof Bologna
DESCRIPTION: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. \n\n\n\nAt Obelis\, we support companies in navigating complex cosmetics regulatory landscapes\, enabling confident and efficient access to global markets. \n\n\n\nWhat you can expect when you meet us at Cosmoprof Bologna: \n\n\n\n✅ Strategic advice on expanding into international markets✅ Clear guidance on regulatory and compliance requirements for your product category✅ Practical support to streamline approvals and reduce time to market \n\n\n\nLet’s plan ahead. Book a slot with our experts and make the most of your visit.  \n\n\n\nLooking forward to connecting with you at Cosmoprof Bologna!
URL:https://www.obelis.net/events/cosmoprof-bologna/
CATEGORIES:Exhibitions
ATTACH;FMTTYPE=image/jpeg:https://www.obelis.net/wp-content/uploads/2026/01/Event-Calendar-Featured-Image-19.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Brussels:20260312T150000
DTEND;TZID=Europe/Brussels:20260312T160000
DTSTAMP:20260407T131944
CREATED:20260302T111932Z
LAST-MODIFIED:20260306T100841Z
UID:10000039-1773327600-1773331200@www.obelis.net
SUMMARY:Powering Compliance: EU Battery Regulation for Portable Batteries
DESCRIPTION: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 | 15:00-16:00 CET \n\n\n\n📌 Where: Online | Zoho Webinars  \n\n\n\n🎬 Guests: Simona Varrella (Obelis Group | Senior RII International Specialist – Regulatory Intelligence & Innovation) and Pablo Antiñanco (Director at RoHS or not)
URL:https://www.obelis.net/events/powering-compliance-eu-battery-regulation-for-portable-batteries-webinar/
CATEGORIES:Webinars
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END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Brussels:20260224T090000
DTEND;TZID=Europe/Brussels:20260225T180000
DTSTAMP:20260407T131944
CREATED:20260115T090933Z
LAST-MODIFIED:20260115T101854Z
UID:10000029-1771923600-1772042400@www.obelis.net
SUMMARY:10th ERPA Annual Summit
DESCRIPTION:A New Milestone in Cosmetics Compliance & Safety\n\n\n\nIn 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. \n\n\n\nNow reintroduced as the ERPA Annual Summit\, this transformation responds to the growing demand for clarity\, meaningful dialogue\, and collaboration across the regulatory and scientific landscape of cosmetics compliance. \n\n\n\nObelis Group is proud to support this milestone edition as a Contributing Partner of the 10th ERPA Annual Summit. \n\n\n\n📅24-25 February 2026 \n\n\n\n📍Leiden University\, Netherlands \n\n\n\nDiscover more at: 10th ERPA Annual Summit 2026 | Home | Cosmetics Compliance & Safety \n\n\n\nGet 15% off! Send us a message at mg@obelis.net
URL:https://www.obelis.net/events/10th-erpa-annual-summit/
CATEGORIES:Exhibitions
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END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Brussels:20260212T150000
DTEND;TZID=Europe/Brussels:20260212T160000
DTSTAMP:20260407T131944
CREATED:20260122T142030Z
LAST-MODIFIED:20260122T142033Z
UID:10000035-1770908400-1770912000@www.obelis.net
SUMMARY:How 2026 Bans & Cosmetic Rules Will Impact Your Business?
DESCRIPTION: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.  \n\n\n\nJoin our LIVE session where we’ll break down the most important 2026 regulatory shifts and show you exactly how to stay compliant\, competitive and ready for growth. You’ll leave with concrete insights to protect your formulas\, update your labelling and confidently navigate each region’s new expectations.   \n\n\n\n \n\n\n\n\n\n\n\n🎯 When: February 12 | 15:00-16:00 CET \n\n\n\n📌 Where: Online | Zoho Webinars  \n\n\n\n🎬 Guests: Sofia Rocha (Obelis Group | Expert Consultant – Regulatory Affairs) & Giorgia Peotta (Obelis Group | RA Regional Consultant – Regulatory Intelligence & Innovation) \n\n\n\n \n\n\n\n \n\n\n\n\nRegister here!
URL:https://www.obelis.net/events/how-2026-bans-cosmetic-rules-will-impact-your-business/
CATEGORIES:Webinars
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END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Brussels:20260209T090000
DTEND;TZID=Europe/Brussels:20260212T180000
DTSTAMP:20260407T131944
CREATED:20251114T113133Z
LAST-MODIFIED:20251114T113137Z
UID:10000024-1770627600-1770919200@www.obelis.net
SUMMARY:WHX DUBAI - Former Arab Health
DESCRIPTION: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! \n\n\n\nAt Obelis\, we help companies navigate complex medical devices and IVDs regulatory landscapes so they can enter markets with confidence and speed. \n\n\n\nWhat You Can Expect When You Meet Us at WHX Dubai \n\n\n\n✅ Strategic advice on expensing into global markets✅ Clear guidance on compliance requirements for your product category✅ Practical support to streamline approvals and reduce time-to-market \n\n\n\nLet’s plan ahead. Book a slot with our experts and make the most of your visit.  \n\n\n\nLooking forward to connecting with you at WHX Dubai!
URL:https://www.obelis.net/events/whx-dubai-former-arab-health/
CATEGORIES:Exhibitions
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END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Brussels:20260129T150000
DTEND;TZID=Europe/Brussels:20260129T160000
DTSTAMP:20260407T131944
CREATED:20260107T151340Z
LAST-MODIFIED:20260121T084551Z
UID:10000028-1769698800-1769702400@www.obelis.net
SUMMARY:EUDAMED\, Swissdamed & IVDR Legacy: What You Need to Know
DESCRIPTION: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 the legacy of IVDR\, ensuring a smooth transition from the previous regulatory framework.  \n\n\n\nWhether you are a manufacturer\, distributor\, or regulatory professional\, this webinar will equip you with practical insights to navigate compliance and stay ahead in the evolving regulatory landscape. \n\n\n\n \n\n\n\n\n\n\n\n🎯 When: January 29 | 15:00-16:00 CET \n\n\n\n📌 Where: Online | Zoho Webinars  \n\n\n\n🎬 Guests: Sandra Ferretti (Obelis Group – CCO) & Georgios Mariolos (Obelis Group – Legal Regional Consultant) \n\n\n\n \n\n\n\n \n\n\n\n\nRegister here!
URL:https://www.obelis.net/events/eudamed-swissdamed-ivdr-legacy-what-you-need-to-know/
CATEGORIES:Webinars
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END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Brussels:20260121T000000
DTEND;TZID=Europe/Brussels:20260331T235959
DTSTAMP:20260407T131944
CREATED:20260119T120409Z
LAST-MODIFIED:20260121T084922Z
UID:10000031-1768953600-1775001599@www.obelis.net
SUMMARY:Benzophenone‑3 & Methyl Salicylate Restrictions  – January and March 2026
DESCRIPTION:United Kingdom – Benzophenone‑3 & Methyl Salicylate Restrictions Deadlines\n\n\n\n✅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. \n\n\n\n✅31 March 2026: Cosmetic products containing Methyl Salicylate (CAS 119-36-8)and not complying with the restrictions outlined in Annex III can no longer be made available on Great Britain’s market. For full details on the restrictions\, please refer to this link. \n\n\n\nCheck your product portfolio now to ensure compliance with the upcoming UK cosmetic ingredient restrictions and avoid market disruptions. Appoint Obelis now to manage your compliance.
URL:https://www.obelis.net/events/benzophenone%e2%80%913-methyl-salicylate-restrictions-january-and-march-2026/
CATEGORIES:Deadlines
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END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Brussels:20260101T000000
DTEND;TZID=Europe/Brussels:20260101T235959
DTSTAMP:20260407T131944
CREATED:20260121T132507Z
LAST-MODIFIED:20260121T132516Z
UID:10000033-1767225600-1767311999@www.obelis.net
SUMMARY:France: Ban Effective Date – January 2026
DESCRIPTION:France – PFAS prohibition effective date\n\n\n\n✅01 January 2026: New prohibition for making available on the market products containing intentionally added PFAS \n\n\n\n \n\n\n\nThe 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 new requirements efficiently and confidently.
URL:https://www.obelis.net/events/france-ban-effective-date-january-2026/
CATEGORIES:Deadlines
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END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Brussels:20260101T000000
DTEND;TZID=Europe/Brussels:20260101T235959
DTSTAMP:20260407T131944
CREATED:20260121T131125Z
LAST-MODIFIED:20260121T131130Z
UID:10000034-1767225600-1767311999@www.obelis.net
SUMMARY:Switzerland: Effective Date of Furocoumarin Restriction
DESCRIPTION:Switzerland – Effective Date of Furocoumarin Restriction\n\n\n\n✅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 normal or reasonably foreseeable conditions of use\, the cosmetic product: is not rinsed off; and may be directly exposed to sunlight. \n\n\n\n \n\n\n\nContact Obelis for expert guidance to ensure full compliance with the upcoming furocoumarin restrictions.
URL:https://www.obelis.net/events/switzerland-effective-date-of-furocoumarin-restriction/
CATEGORIES:Deadlines
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END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Brussels:20251211T160000
DTEND;TZID=Europe/Brussels:20251211T170000
DTSTAMP:20260407T131944
CREATED:20251126T125657Z
LAST-MODIFIED:20251126T125701Z
UID:10000025-1765468800-1765472400@www.obelis.net
SUMMARY:WEBINAR: ISO 13485:2016 & EU MDR/IVDR – From Scope to Certification
DESCRIPTION: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 explanations and practical checklists\, we will cover:– The scope of ISO 13485 and affected roles (manufacturers\, ARs\, importers\, distributors)– Its relationship with EU MDR/IVDR\, CE marking\, and registrations in specific markets– The main clauses of the standard and what they expect from you– The essential documents and records you must have in place– The steps to achieve and maintain certification\, and where our service fits into each stage👉 Reserve your spot now and take a concrete step towards a stronger\, ISO 13485-compliant QMS.
URL:https://www.obelis.net/events/webinar-iso-134852016-eu-mdr-ivdr-from-scope-to-certification/
CATEGORIES:Exhibitions
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END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Brussels:20251117T090000
DTEND;TZID=Europe/Brussels:20251120T180000
DTSTAMP:20260407T131944
CREATED:20250221T100326Z
LAST-MODIFIED:20250625T100957Z
UID:10000010-1763370000-1763661600@www.obelis.net
SUMMARY:MEDICA 2025 - Düsseldorf
DESCRIPTION:Heard about MEDICA? It is one of the largest medical B2B trade fairs in the world and we will be there to support you! \n\n\n\nOur goal is to assist your company in smoothly complying with global regulations. \n\n\n\nWhy Meet Us at MEDICA? \n\n\n\n✅ Expert insights on market access & compliance✅ Tailored strategies to accelerate approvals✅ Guidance on the latest regulatory updates \n\n\n\nSchedule a meeting in advance and let’s chat at the exhibition! \n\n\n\nSee you at MEDICA!
URL:https://www.obelis.net/events/medica-2025-dusseldorf/
CATEGORIES:Exhibitions
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END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Brussels:20251016T160000
DTEND;TZID=Europe/Brussels:20251016T170000
DTSTAMP:20260407T131944
CREATED:20251003T090632Z
LAST-MODIFIED:20251003T091343Z
UID:10000023-1760630400-1760634000@www.obelis.net
SUMMARY:EU vs Turkish Cosmetics Regulations: Key Differences and Compliance Pathways
DESCRIPTION: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 stay compliant and avoid costly delays. \n\n\n\nWebinar in Focus:✅Turkish vs. EU notification systems \n\n\n\n✅RP obligations \n\n\n\n✅Labeling requirements \n\n\n\n✅ and much more… \n\n\n\n\n\n\n\n🎯 When: October 16 | 14:00-17:00 CET \n\n\n\n📌 Where: Online | Zoho Webinars  \n\n\n\n🎬 Guests: Katie Gallagher (Obelis Group) & A. Selim Erol (Macro Professional) \n\n\n\n \n\n\n\n \n\n\n\n\nRegister here!
URL:https://www.obelis.net/events/eu-vs-turkish-cosmetics-regulations-key-differences-and-compliance-pathways/
CATEGORIES:Webinars
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END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Brussels:20250930T150000
DTEND;TZID=Europe/Brussels:20250930T160000
DTSTAMP:20260407T131944
CREATED:20250923T102133Z
LAST-MODIFIED:20250923T102818Z
UID:10000022-1759244400-1759248000@www.obelis.net
SUMMARY:Navigating Canadian Ingredient Approval and the EU/UK Split
DESCRIPTION:Cosmetic regulations are evolving quickly\, are you keeping up?  \n\n\n\nJoin 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 approvals and adapt your compliance strategy across markets.  \n\n\n\nWebinar highlights :✅ Canada’s Cosmetic Ingredient Hotlist: Purpose\, update process\, and what it means✅ Canada & EU Regulatory Frameworks: Points for divergence and areas of alignment✅ EU & UK Regulatory Frameworks: Key divergences following Brexit and their implications for compliance \n\n\n\n\n\n\n\n🎯 When: September 30 | 15:00-16:00 CET \n\n\n\n📌 Where: Online | Zoho Webinars  \n\n\n\n🎬 Guests: Chiara Lai (Obelis Group) \n\n\n\n \n\n\n\n \n\n\n\n\nRegister here!
URL:https://www.obelis.net/events/navigating-canadian-ingredient-approval-and-the-eu-uk-split/
CATEGORIES:Webinars
ATTACH;FMTTYPE=image/jpeg:https://www.obelis.net/wp-content/uploads/2025/09/Event-Calendar-Featured-Image-2.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Brussels:20250909T160000
DTEND;TZID=Europe/Brussels:20250909T170000
DTSTAMP:20260407T131944
CREATED:20250818T130334Z
LAST-MODIFIED:20250827T122445Z
UID:10000020-1757433600-1757437200@www.obelis.net
SUMMARY:EUDAMED & Swissdamed Explained: Key Modules and Timelines for Medical Devices
DESCRIPTION: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.  \n\n\n\nWebinar highlights include: \n\n\n\n✅What is public? \n\n\n\n✅Code Usage \n\n\n\n✅Timelines \n\n\n\n✅Client Experiences to date \n\n\n\n\n\n\n\n🎯 When: September 9 | 16:00-17:00 CET \n\n\n\n📌 Where: Online | Zoho Webinars  \n\n\n\n🎬 Guests: Richard Houlihan (EirMed) and Georgios Mariolos (Obelis Group) \n\n\n\n \n\n\n\n \n\n\n\n\nRegister here!
URL:https://www.obelis.net/events/eudamed-swissdamed-explained-key-modules-and-timelines-for-medical-devices/
CATEGORIES:Webinars
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END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Brussels:20250727T090000
DTEND;TZID=Europe/Brussels:20250731T180000
DTSTAMP:20260407T131944
CREATED:20250221T095942Z
LAST-MODIFIED:20250602T091902Z
UID:10000009-1753606800-1753984800@www.obelis.net
SUMMARY:ADLM 2025 - Chicago
DESCRIPTION: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 up a meeting in advance and let’s discuss it together at your booth.Looking forward to meet you at ADML Chicago!
URL:https://www.obelis.net/events/adlm-2025-chicago/
CATEGORIES:Exhibitions
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END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Brussels:20250715T090000
DTEND;TZID=Europe/Brussels:20250717T180000
DTSTAMP:20260407T131944
CREATED:20250221T095509Z
LAST-MODIFIED:20250602T083928Z
UID:10000008-1752570000-1752775200@www.obelis.net
SUMMARY:COSMOPROF 2025 - Las Vegas
DESCRIPTION: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 advance\, and we’ll see you at your booth.Meet you there!
URL:https://www.obelis.net/events/cosmoprof-2025-las-vegas/
CATEGORIES:Exhibitions
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END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Brussels:20250710T160000
DTEND;TZID=Europe/Brussels:20250710T170000
DTSTAMP:20260407T131944
CREATED:20250701T150142Z
LAST-MODIFIED:20250701T150205Z
UID:10000019-1752163200-1752166800@www.obelis.net
SUMMARY:GB/UK Post Market Surveillance: What You Need to Know
DESCRIPTION:Navigating the evolving regulatory landscape in the UK can be complex\, especially when it comes to Post Market Surveillance (PMS).  \n\n\n\nJoin 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\, or part of a compliance or quality team\, this session is your guide to ensuring ongoing product safety and regulatory alignment in the UK market.  \n\n\n\nHere’s some of what you can expect to learn: \n\n\n\n✅PMS Regulation & Scope \n\n\n\n✅Manufacturer Responsibilities  \n\n\n\n✅Risk Management & CAPA  \n\n\n\n✅Communication & Roles  \n\n\n\n \n\n\n\n\n\n\n\n🎯 When: July 10 | 16:00-17:00 CET \n\n\n\n📌 Where: Online | Zoho Webinars  \n\n\n\n🎬 Guests: Alison Hinchliffe (KIWA) and Homer Trieu (Obelis Group) \n\n\n\n \n\n\n\n \n\n\n\n\nRegister here!
URL:https://www.obelis.net/events/gb-uk-post-market-surveillance-what-you-need-to-know/
CATEGORIES:Webinars
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BEGIN:VEVENT
DTSTART;TZID=Europe/Brussels:20250611T090000
DTEND;TZID=Europe/Brussels:20250613T180000
DTSTAMP:20260407T131944
CREATED:20250221T094656Z
LAST-MODIFIED:20250521T103111Z
UID:10000007-1749632400-1749837600@www.obelis.net
SUMMARY:FIME 2025 - Miami
DESCRIPTION: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. \n\n\n\nWhy Meet Us at FIME? \n\n\n\n✅ Expert insights on market access & compliance✅ Tailored strategies to accelerate approvals✅ Guidance on the latest regulatory updates \n\n\n\nWe’re here to support your regulatory journey\, let’s talk! Set up a meeting in advance\, and we’ll see you at your booth. \n\n\n\nSee you at FIME!
URL:https://www.obelis.net/events/fime-2025-miami/
CATEGORIES:Exhibitions
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BEGIN:VEVENT
DTSTART;TZID=Europe/Brussels:20250603T090000
DTEND;TZID=Europe/Brussels:20250604T230000
DTSTAMP:20260407T131944
CREATED:20250221T092327Z
LAST-MODIFIED:20250515T111015Z
UID:10000006-1748941200-1749078000@www.obelis.net
SUMMARY:NYSCC 2025 - New York
DESCRIPTION: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 the latest regulatory updatesConnect with us to discover tailored solutions for your regulatory needs. Schedule a meeting today\, and let’s chat at the event!Looking forward to meet you at NYSCC!
URL:https://www.obelis.net/events/nyscc-2025-new-york/
CATEGORIES:Exhibitions
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BEGIN:VEVENT
DTSTART;TZID=Europe/Brussels:20250526T000000
DTEND;TZID=Europe/Brussels:20250526T235959
DTSTAMP:20260407T131944
CREATED:20250221T132101Z
LAST-MODIFIED:20250519T092253Z
UID:10000012-1748217600-1748303999@www.obelis.net
SUMMARY:IVDR Legacy Extension Deadline – May 2025
DESCRIPTION: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: \n\n\n\nSubmission of an application to a Notified Body \n\n\n\n✅ Class D devices (high-risk IVDs that were self-certified under IVDD but now require a Notified Body under IVDR)- by 26 September 2025 \n\n\n\n✅ Class C devices – by 26 May 2026 \n\n\n\n✅ Class B & Class A sterile devices – by 26 May 2027 \n\n\n\n✅All classes of IVD legacy devices – Implementation of an IVDR-compliant Quality Management System (QMS) – by 26 May 2025 \n\n\n\nFailing to meet these and existing legacy conditions means the extension will not apply\, and full IVDR compliance will be required. Manufacturers should act now to ensure a smooth transition and avoid market disruptions. \n\n\n\nIs your company on track for compliance? Let’s discuss how to navigate this critical regulatory shift. \n\n\n\n \n\n\n\n\n\n\n\n\nLegacy device manufacturers: Important deadlines & steps · MDlaw – Information platform on European medical device regulations: The Critical Role of the Responsible Technical Person
URL:https://www.obelis.net/events/ivdr-legacy-extension-deadline-may-2025/
CATEGORIES:Deadlines
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BEGIN:VEVENT
DTSTART;TZID=Europe/Brussels:20250508T163000
DTEND;TZID=Europe/Brussels:20250508T173000
DTSTAMP:20260407T131944
CREATED:20250416T141017Z
LAST-MODIFIED:20250422T144459Z
UID:10000018-1746721800-1746725400@www.obelis.net
SUMMARY:FDA U.S. Agent and Submissions
DESCRIPTION: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: \n\n\n\n✅Cybersecurity  \n\n\n\n✅U.S. Agent and Official Correspondent \n\n\n\n✅Establishment Registration and Device Listing \n\n\n\n✅Submissions (GUDID\, 510k and others) \n\n\n\n\n\n\n\n🎯 When: May 8 | 16:30-17:30 CET \n\n\n\n📌 Where: Online | Zoho Webinars  \n\n\n\n🎬 Guests: Jay Mansour (Mansour Consulting LLC) and Tommaso Poles (Obelis Group) \n\n\n\n \n\n\n\n \n\n\n\n\nRegister here!
URL:https://www.obelis.net/events/fda-u-s-agent-and-submissions/
CATEGORIES:Webinars
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BEGIN:VEVENT
DTSTART;TZID=Europe/Brussels:20250508T100000
DTEND;TZID=Europe/Brussels:20250510T180000
DTSTAMP:20260407T131944
CREATED:20250221T091600Z
LAST-MODIFIED:20250327T104329Z
UID:10000005-1746698400-1746900000@www.obelis.net
SUMMARY:Beauty Istanbul 2025 - Istanbul
DESCRIPTION: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 and discuss how we can support your regulatory needs. Book a meeting with us in advance and see you at your booth!We look forward to meeting you at Beauty Istanbul!
URL:https://www.obelis.net/events/beauty-istanbul-2025-istanbul/
CATEGORIES:Exhibitions
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BEGIN:VEVENT
DTSTART;TZID=Europe/Brussels:20250422T150000
DTEND;TZID=Europe/Brussels:20250422T160000
DTSTAMP:20260407T131944
CREATED:20250328T091352Z
LAST-MODIFIED:20250328T092432Z
UID:10000017-1745334000-1745337600@www.obelis.net
SUMMARY:GPSR\, VAT Compliance\, and Customs: Essential Insights for Market Entry
DESCRIPTION: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! \n\n\n\nHere’s what you can expect to learn: \n\n\n\n✅VAT requirements for selling in the EU \n\n\n\n✅Overview of EPR and category distinctions by country \n\n\n\n✅Insights into customs clearance and shipping services \n\n\n\n\n\n\n\n🎯 When: April 22nd | 15:00-16:00 CET \n\n\n\n📌 Where: Online | Zoho Webinars  \n\n\n\n🎬 Guests: Patryk Czepulonis (Avask Group)\, Khaled Khaled (Avask Group) and Katerina Svambergova (Obelis Group) \n\n\n\n \n\n\n\n \n\n\n\n\nRegister here!
URL:https://www.obelis.net/events/gpsr-vat-compliance-and-customs-essential-insights-for-market-entry/
CATEGORIES:Webinars
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BEGIN:VEVENT
DTSTART;TZID=Europe/Brussels:20250420T000000
DTEND;TZID=Europe/Brussels:20250420T235959
DTSTAMP:20260407T131944
CREATED:20250225T162203Z
LAST-MODIFIED:20250327T104820Z
UID:10000014-1745107200-1745193599@www.obelis.net
SUMMARY:UK Cosmetics Market: banned CMRs – April 2025
DESCRIPTION:On October 3\, 2024\, the United Kingdom took a significant step toward tightening cosmetic safety by notifying the World Trade Organization (WTO) of a draft amendment to its GB Cosmetics Regulation.  \n\n\n\nThis update introduces 13 more chemicals to the growing list of banned substances\, all of which are classified as carcinogenic\, mutagenic\, or reprotoxic (CMR). \n\n\n\nThis move follows an earlier major shift in 2024\, when 52 CMR chemicals were banned through the same legislative change. However\, it’s important to note that there are still 13 substances banned in the EU that remain legal in the UK\, leaving room for further regulatory alignment. \n\n\n\nWant more details on which ingridients are banned? \n\n\n\n\n\n\n\n\nUK Bans 13 Additional CMR Chemicals in Cosmetics – COSlaw.eu – Guiding through EU Cosmetics Regulations: The Critical Role of the Responsible Technical Person
URL:https://www.obelis.net/events/uk-crm-pom-april-2025/
CATEGORIES:Deadlines
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BEGIN:VEVENT
DTSTART;TZID=Europe/Brussels:20250417T110000
DTEND;TZID=Europe/Brussels:20250417T120000
DTSTAMP:20260407T131944
CREATED:20250318T141903Z
LAST-MODIFIED:20250328T092631Z
UID:10000016-1744887600-1744891200@www.obelis.net
SUMMARY:EUDAMED & National Registration: Navigating Compliance for Medical Devices
DESCRIPTION: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 more! \n\n\n\nWebinar highlights include: \n\n\n\n✅How to Perform National Registrations – Step-by-step guidance and how Obelis can help \n\n\n\n✅Pro Tips for Success – Practical advice to optimize your EUDAMED journey \n\n\n\n✅EU Countries Requiring National Registration – A quick recap of current requirements \n\n\n\n\n\n\n\n🎯 When: April 17th | 11:00-12:00 CET \n\n\n\n📌 Where: Online | Zoho Webinars  \n\n\n\n🎬 Guests: Richard Houlihan (EirMed) & Carlos Francisco Marin Barrios (Obelis Group) \n\n\n\n \n\n\n\n \n\n\n\n\nRegister here!
URL:https://www.obelis.net/events/eudamed-national-registration-navigating-compliance-for-medical-devices/
CATEGORIES:Webinars
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BEGIN:VEVENT
DTSTART;TZID=Europe/Brussels:20250325T090000
DTEND;TZID=Europe/Brussels:20250328T173000
DTSTAMP:20260407T131944
CREATED:20250212T121828Z
LAST-MODIFIED:20250327T105523Z
UID:10000003-1742893200-1743183000@www.obelis.net
SUMMARY:IDS 2025 - Cologne
DESCRIPTION:Bringing Your Dental Devices to Market? Join us at IDS\, the world’s leading trade show for dental innovation! We’re here to help dental and medical device manufacturers easily navigate global regulations.  \n\n\n\nWhy Meet Us at IDS? \n\n\n\n✅ Expert insights on market access & compliance✅ Tailored strategies to accelerate approvals✅ Guidance on the latest regulatory updates \n\n\n\nLet’s connect and discuss how we can support your regulatory needs. Book a meeting with us in advance or visit our booth at the event! \n\n\n\nWe look forward to seeing you at IDS!
URL:https://www.obelis.net/events/ids-2025-cologne/
CATEGORIES:Exhibitions
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BEGIN:VEVENT
DTSTART;TZID=Europe/Brussels:20250320T090000
DTEND;TZID=Europe/Brussels:20250323T180000
DTSTAMP:20260407T131944
CREATED:20250304T101432Z
LAST-MODIFIED:20250327T105716Z
UID:10000015-1742461200-1742752800@www.obelis.net
SUMMARY:COSMOPROF 2025 - Bologna
DESCRIPTION:Product launches and innovative solutions? Counting you in for Cosmoprof Bologna! \n\n\n\nOur goal is to assist your company in smoothly complying with global regulations and we will be there to support you. \n\n\n\nWhy Meet Us at Cosmoprof Bologna? \n\n\n\n✅ Expert insights on market access & compliance✅ Tailored strategies to accelerate approvals✅ Guidance on the latest regulatory updates \n\n\n\nSchedule a meeting in advance and let’s become compliant together\, step by step! \n\n\n\nSee you in Bologna!
URL:https://www.obelis.net/events/cosmoprof-2025-bologna/
CATEGORIES:Exhibitions
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END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Brussels:20250318T160000
DTEND;TZID=Europe/Brussels:20250318T170000
DTSTAMP:20260407T131944
CREATED:20250221T132636Z
LAST-MODIFIED:20250327T105916Z
UID:10000011-1742313600-1742317200@www.obelis.net
SUMMARY:Notified Bodies for IVD (EU vs CANADA)
DESCRIPTION: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. \n\n\n\nOur exclusive webinar will cover: \n\n\n\n✅Strategies for efficient regulatory compliance in both regions \n\n\n\n✅Key differences between EU IVDR and Health Canada requirements \n\n\n\n✅The role of Notified Bodies and how they impact IVD approvals \n\n\n\n\n\n\n\n🎯 When: March 18th | 16:00-17:00 CET \n\n\n\n📌 Where: Online | Zoho Webinars  \n\n\n\n🎬 Guests: TUV (EU perspective) & PASB (Canadian perspective) \n\n\n\n \n\n\n\n\nRegister here!
URL:https://www.obelis.net/events/notified-bodies-for-ivd-eu-vs-canada/
CATEGORIES:Webinars
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END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Brussels:20250301T000000
DTEND;TZID=Europe/Brussels:20250330T235959
DTSTAMP:20260407T131944
CREATED:20250225T161924Z
LAST-MODIFIED:20250327T110209Z
UID:10000013-1740787200-1743379199@www.obelis.net
SUMMARY:Canadian RP Deadline – April 2025
DESCRIPTION:The Cosmetic Regulations were amended in April 2024 to – among other things – expand the definition of “manufacturer” to mean:  \n\n\n\n💠A person in Canada who sells the cosmetic under their own name or a trademark\, design\, trade name\, or other mark they own or control. \n\n\n\n💠A person in Canada authorized to act on behalf of a non-Canadian entity that sells the cosmetic under its own name or trademark. \n\n\n\nThis means that\, to sell in Canada\, a brand owner based outside the country must appoint a representative with a Canadian address who assumes the legal obligations of a manufacturer. \n\n\n\nAlthough these amendments have been in force since October 2024\, Health Canada has announced that starting March 2025\, they will officially be enforced with the updated notification form requiring the name and address of the representative for brand owners in Canada. 
URL:https://www.obelis.net/events/canadian-rp-april-2025/
CATEGORIES:Deadlines
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