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DTSTART;TZID=Europe/Brussels:20260506T113000
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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
ATTACH;FMTTYPE=image/jpeg:https://www.obelis.net/wp-content/uploads/2026/04/Event-Calendar-Featured-Image-29.jpg
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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
ATTACH;FMTTYPE=image/jpeg:https://www.obelis.net/wp-content/uploads/2026/05/EUDAMED-webinar-.jpg
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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
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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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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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