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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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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: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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BEGIN:VEVENT
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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BEGIN:VEVENT
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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BEGIN:VEVENT
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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BEGIN:VEVENT
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
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BEGIN:VEVENT
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
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END:VEVENT
BEGIN:VEVENT
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
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BEGIN:VEVENT
DTSTART;TZID=Europe/Brussels:20260212T150000
DTEND;TZID=Europe/Brussels:20260212T160000
DTSTAMP:20260122T142033Z
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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BEGIN:VEVENT
DTSTART;TZID=Europe/Brussels:20260129T150000
DTEND;TZID=Europe/Brussels:20260129T160000
DTSTAMP:20260121T084551Z
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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BEGIN:VEVENT
DTSTART;TZID=Europe/Brussels:20251016T160000
DTEND;TZID=Europe/Brussels:20251016T170000
DTSTAMP:20251003T091343Z
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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BEGIN:VEVENT
DTSTART;TZID=Europe/Brussels:20250930T150000
DTEND;TZID=Europe/Brussels:20250930T160000
DTSTAMP:20250923T102818Z
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
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BEGIN:VEVENT
DTSTART;TZID=Europe/Brussels:20250909T160000
DTEND;TZID=Europe/Brussels:20250909T170000
DTSTAMP:20250827T122445Z
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:20250710T160000
DTEND;TZID=Europe/Brussels:20250710T170000
DTSTAMP:20250701T150205Z
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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END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Brussels:20250508T163000
DTEND;TZID=Europe/Brussels:20250508T173000
DTSTAMP:20250422T144459Z
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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END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Brussels:20250422T150000
DTEND;TZID=Europe/Brussels:20250422T160000
DTSTAMP:20250328T092432Z
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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DTSTART;TZID=Europe/Brussels:20250417T110000
DTEND;TZID=Europe/Brussels:20250417T120000
DTSTAMP:20250328T092631Z
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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DTSTART;TZID=Europe/Brussels:20250318T160000
DTEND;TZID=Europe/Brussels:20250318T170000
DTSTAMP:20250327T105916Z
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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