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X-WR-CALDESC:Events for Obelis Group
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BEGIN:VEVENT
DTSTART;TZID=Europe/Brussels:20260526T000000
DTEND;TZID=Europe/Brussels:20260526T235959
DTSTAMP:20260522T192503
CREATED:20260127T081634Z
LAST-MODIFIED:20260127T082030Z
UID:10000037-1779753600-1779839999@www.obelis.net
SUMMARY:IVDR Class C Transitional Deadline – May 2026
DESCRIPTION: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. \n\n\n\nFor these devices\, the following milestones apply:  \n\n\n\n✅A written agreement between the manufacturer and the Notified Body must be signed by 26 September 2026. \n\n\n\n✅The manufacturer or their Authorised Representative must apply to a Notified Body for IVDR conformity assessment by 26 May 2026. \n\n\n\nObelis guides manufacturers through the IVDR transition\, including selecting and engaging with a Notified Body.
URL:https://www.obelis.net/events/ivdr-class-c-transitional-deadline-may-2026/
CATEGORIES:Deadlines
ATTACH;FMTTYPE=image/jpeg:https://www.obelis.net/wp-content/uploads/2026/01/331.jpg
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BEGIN:VEVENT
DTSTART;TZID=Europe/Brussels:20260528T000000
DTEND;TZID=Europe/Brussels:20260528T235959
DTSTAMP:20260522T192503
CREATED:20260127T081040Z
LAST-MODIFIED:20260127T081211Z
UID:10000036-1779926400-1780012799@www.obelis.net
SUMMARY:EUDAMED Registration Becomes Mandatory – May 2026
DESCRIPTION:Regulatory Alert | EUDAMED becomes mandatory\n\n\n\nCommission 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. \n\n\n\nMandatory modules from 28 May 2026: \n\n\n\n✅Market Surveillance \n\n\n\n✅Actors: registration of manufacturers\, authorised representatives\, importers \n\n\n\n✅UDI / Devices: device registration (excluding custom-made devices) \n\n\n\n✅Notified Bodies & Certificates \n\n\n\nA six-month transition period (until November 27\, 2026) applies only to devices placed on the market before May 28\, 2026. Devices placed on the market after this date must be registered before market access. \n\n\n\nObelis supports manufacturers at every step of EUDAMED compliance!
URL:https://www.obelis.net/events/eudamed-registration-becomes-mandatory-may-2026/
CATEGORIES:Deadlines
ATTACH;FMTTYPE=image/jpeg:https://www.obelis.net/wp-content/uploads/2026/01/341.jpg
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BEGIN:VEVENT
DTSTART;TZID=Europe/Brussels:20260528T150000
DTEND;TZID=Europe/Brussels:20260528T160000
DTSTAMP:20260522T192503
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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BEGIN:VEVENT
DTSTART;TZID=Europe/Brussels:20260604T150000
DTEND;TZID=Europe/Brussels:20260604T160000
DTSTAMP:20260522T192503
CREATED:20260520T092200Z
LAST-MODIFIED:20260520T092205Z
UID:10000049-1780585200-1780588800@www.obelis.net
SUMMARY:Webinar - Global Cosmetic Safety: Mastering Multiterritory Assessment & Laboratory Testing
DESCRIPTION:Join us for an expert-led session on navigating cosmetic safety in a complex global regulatory landscape. \n\n\n\nAs 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. \n\n\n\nIn this webinar\, we will explore how laboratory testing supports product safety and regulatory acceptance across different markets\, and how to effectively manage multiterritory cosmetic safety assessments without duplicating efforts. You’ll also gain insights into the concept of “living documentation”\, and why maintaining up-to-date safety files is essential to stay compliant in an evolving regulatory environment.
URL:https://www.obelis.net/events/webinar-global-cosmetic-safety-mastering-multiterritory-assessment-laboratory-testing/
CATEGORIES:Deadlines
ATTACH;FMTTYPE=image/jpeg:https://www.obelis.net/wp-content/uploads/2026/05/Event-Calendar-Featured-Image.jpg
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DTSTART;TZID=Europe/Brussels:20260609T150000
DTEND;TZID=Europe/Brussels:20260609T160000
DTSTAMP:20260522T192503
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:20260713T000000
DTEND;TZID=Europe/Brussels:20260715T235959
DTSTAMP:20260522T192503
CREATED:20260522T071650Z
LAST-MODIFIED:20260522T084243Z
UID:10000051-1783900800-1784159999@www.obelis.net
SUMMARY:Cosmoprof Las Vegas 2026
DESCRIPTION:Passionate about cosmetics and beauty innovation? Meet us at Cosmoprof Las Vegas this July! \n\n\n\nAt Obelis Group\, we help cosmetic brands simplify global regulatory compliance and confidently expand into international markets.Why Meet Us at Cosmoprof Las Vegas 2026?✅ Expert guidance on market access & compliance✅ Tailored regulatory strategies to support your market expansion goals ✅ Support on the latest regulatory updatesSchedule a meeting with us in advance\, and we’ll be happy to meet at our booth or wherever is most convenient for you during the exhibition.We look forward to meeting you at Cosmoprof Las Vegas!
URL:https://www.obelis.net/events/obelis-at-cosmoprof-las-vegas-2026/
CATEGORIES:Exhibitions
ATTACH;FMTTYPE=image/jpeg:https://www.obelis.net/wp-content/uploads/2026/05/Cosmoprof-Vegas.jpg
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BEGIN:VEVENT
DTSTART;TZID=Europe/Brussels:20260731T000000
DTEND;TZID=Europe/Brussels:20260731T235959
DTSTAMP:20260522T192503
CREATED:20260420T132148Z
LAST-MODIFIED:20260420T151517Z
UID:10000046-1785456000-1785542399@www.obelis.net
SUMMARY:EU Fragrance Allergens Deadline
DESCRIPTION:Starting on 31 July 2026\, cosmetic products placed on the EU market must comply with the updated labelling requirements\, including the disclosure of 56 additional fragrance allergens where applicable. \n\n\n\nFrom this date onwards: \n\n\n\n✅ Products that do not meet the updated labelling requirements may be held at customs\, refused entry\, or removed from the market \n\n\n\n✅ Every new product entering EU customs is treated as a fresh placement on the market; consequently\, all batches arriving after the deadline must meet the updated labeling requirements\, regardless of whether the product was previously available. \n\n\n\nNeed a tailored assessment or product-specific guidance? Our experts are here to help.Not sure if your products are compliant? Contact Obelis for a detailed evaluation.
URL:https://www.obelis.net/events/eu-cosmetics-fragrance-allergens-deadline-2026-labeling-compliance/
CATEGORIES:Deadlines
ATTACH;FMTTYPE=image/jpeg:https://www.obelis.net/wp-content/uploads/2026/04/Deadline-fragrance-1.jpg
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