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DTSTART;TZID=Europe/Brussels:20260121T000000
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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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DTSTART;TZID=Europe/Brussels:20260312T150000
DTEND;TZID=Europe/Brussels:20260312T160000
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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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DTSTART;TZID=Europe/Brussels:20260326T090000
DTEND;TZID=Europe/Brussels:20260328T180000
DTSTAMP:20260418T012850
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
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DTSTART;TZID=Europe/Brussels:20260326T160000
DTEND;TZID=Europe/Brussels:20260326T170000
DTSTAMP:20260418T012850
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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