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DTSTART;TZID=Europe/Brussels:20260312T150000
DTEND;TZID=Europe/Brussels:20260312T160000
DTSTAMP:20260306T100841Z
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
ATTACH;FMTTYPE=image/jpeg:https://www.obelis.net/wp-content/uploads/2026/03/Event-Calendar-Featured-Image-28.jpg
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DTSTART;TZID=Europe/Brussels:20260326T160000
DTEND;TZID=Europe/Brussels:20260326T170000
DTSTAMP:20260323T131642Z
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
ATTACH;FMTTYPE=image/jpeg:https://www.obelis.net/wp-content/uploads/2026/03/US-Labeling-Webinar.jpg
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DTSTART;TZID=Europe/Brussels:20260416T150000
DTEND;TZID=Europe/Brussels:20260416T160000
DTSTAMP:20260331T073459Z
CREATED:20260331T073455Z
LAST-MODIFIED:20260331T073459Z
UID:10000044-1776351600-1776355200@www.obelis.net
SUMMARY:The Critical Role of the Responsible Technical Person
DESCRIPTION: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\, CEO of Obelis TürkiyeReserve your spot now and stay ahead in cosmetic compliance!
URL:https://www.obelis.net/events/cosmetic-compliance-2026-gmp-iso-22716-rtp-webinar/
CATEGORIES:Webinars
ATTACH;FMTTYPE=image/jpeg:https://www.obelis.net/wp-content/uploads/2026/03/Turkiye-webinar-2.jpg
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DTSTART;TZID=Europe/Brussels:20260421T160000
DTEND;TZID=Europe/Brussels:20260421T170000
DTSTAMP:20260106T112158Z
CREATED:20251203T133359Z
LAST-MODIFIED:20260106T112158Z
UID:10000026-1776787200-1776790800@www.obelis.net
SUMMARY:ON-DEMAND WEBINAR: Food Supplements in the EU and UK – a focus on online sales (AMAZON)
DESCRIPTION: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 on Amazon✅ How Obelis can support you as your FBOIdeal for manufacturers\, distributors\, Amazon sellers\, and regulatory professionals looking for a quick\, reliable guide to staying compliant in the EU and UK.
URL:https://www.obelis.net/events/on-demand-webinar-food-supplements-in-the-eu-and-uk-a-focus-on-online-sales-amazon/
CATEGORIES:Webinars
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DTSTART;TZID=Europe/Brussels:20260506T113000
DTEND;TZID=Europe/Brussels:20260506T123000
DTSTAMP:20260414T131248Z
CREATED:20260414T131053Z
LAST-MODIFIED:20260414T131248Z
UID:10000045-1778067000-1778070600@www.obelis.net
SUMMARY:Winning with IVDR: Compliance Strategy\, Class C Pathways & NB Engagement
DESCRIPTION: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. \n\n\n\nWe will also dive into Class C classification and conformity assessment pathways\, highlight the most common clinical evidence gaps identified by Notified Bodies\, and share practical insights on how to work more effectively with Notified Bodies\, including smarter communication and selection strategies to support successful approvals.Join us to gain clarity\, reduce compliance risks\, and strengthen your IVDR strategy. Register now to secure your spot.
URL:https://www.obelis.net/events/winning-with-ivdr-compliance-strategy-class-c-pathways-nb-engagement/
CATEGORIES:Webinars
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DTSTART;TZID=Europe/Brussels:20260528T150000
DTEND;TZID=Europe/Brussels:20260528T160000
DTSTAMP:20260513T094112Z
CREATED:20260513T094110Z
LAST-MODIFIED:20260513T094112Z
UID:10000047-1779980400-1779984000@www.obelis.net
SUMMARY:EUDAMED Readiness for MDR & IVDR: Registration Obligations and Timelines
DESCRIPTION: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. \n\n\n\nDuring 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 legacy devices\, as well as the role of the Authorised Representative in EUDAMED verification processes. \n\n\n\nJoin us to gain a clearer understanding of the upcoming EUDAMED deadline and its impact on medical device and IVD manufacturers operating in the EU.
URL:https://www.obelis.net/events/eudamed-webinar-2026-mdr-ivdr-registration-deadlines/
CATEGORIES:Webinars
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DTSTART;TZID=Europe/Brussels:20260609T150000
DTEND;TZID=Europe/Brussels:20260609T160000
DTSTAMP:20260520T134330Z
CREATED:20260520T133922Z
LAST-MODIFIED:20260520T134330Z
UID:10000050-1781017200-1781020800@www.obelis.net
SUMMARY:EU & UK Detergents Market Access: Regulations & Upcoming EU Changes
DESCRIPTION: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. \n\n\n\nThe webinar will also cover upcoming EU regulatory developments\, highlighting important deadlines\, transition periods\, and grace periods relevant for continued market access. In addition\, we will present Obelis’ Representative and consultancy services\, including product compliance review\, support with UFI code management\, PCN submissions\, and national registrations across EU Member States.
URL:https://www.obelis.net/events/eu-uk-detergents-market-access-regulations/
CATEGORIES:Webinars
ATTACH;FMTTYPE=image/jpeg:https://www.obelis.net/wp-content/uploads/2026/05/Event-Calendar-Featured-Image-1.jpg
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BEGIN:VEVENT
DTSTART;TZID=Europe/Brussels:20260625T150000
DTEND;TZID=Europe/Brussels:20260625T160000
DTSTAMP:20260622T075912Z
CREATED:20260617T141607Z
LAST-MODIFIED:20260622T075912Z
UID:10000052-1782399600-1782403200@www.obelis.net
SUMMARY:Cosmetic Claims Across Borders: Understanding EU and Turkish Requirements
DESCRIPTION:Join our webinar to gain practical insights into cosmetic claims and their growing importance in today’s cosmetics industry. \n\n\n\nDuring 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 from” claims\, including their definition\, common examples\, and the challenges associated with their compliance. \n\n\n\nThe webinar will also provide an overview of cosmetic product claims in Türkiye\, covering key legal requirements\, principles of truthfulness and fair communication\, and best practices for ensuring claims are accurate\, substantiated\, and compliant with applicable regulations.
URL:https://www.obelis.net/events/cosmetic-claims-across-borders-understanding-eu-and-turkish-requirements/
CATEGORIES:Webinars
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BEGIN:VEVENT
DTSTART;TZID=Europe/Brussels:20260708T160000
DTEND;TZID=Europe/Brussels:20260708T170000
DTSTAMP:20260624T083949Z
CREATED:20260624T083418Z
LAST-MODIFIED:20260624T083949Z
UID:10000053-1783526400-1783530000@www.obelis.net
SUMMARY:Think You're FDA Compliant?                California May Require More
DESCRIPTION: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. \n\n\n\nDuring 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 requirements. \n\n\n\nWe will then explore key California cosmetics regulations\, including Proposition 65\, the California Safe Cosmetics Program\, CARB VOC limits\, the California Toxic-Free Cosmetics Act\, and the California PFAS-Free Cosmetics Act. \n\n\n\nParticipants will gain a better understanding of how these requirements interact and the key considerations for achieving compliance in the U.S. cosmetics market.
URL:https://www.obelis.net/events/think-youre-fda-compliant-california-may-require-more/
CATEGORIES:Webinars
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