Meet us at Arab Health 2025
Arab Health 2025 Dubai World Trade Centre, Dubai, United Arab EmiratesObelis goes to Arab Health 2025. Book a meeting.
18 events found.
Events, Webinars and Deadlines
Our calendar informs on industry events, upcoming compliance deadlines, as well as new Obelis webinars.
Canadian RP Deadline – April 2025
The Cosmetic Regulations were amended in April 2024 to – among other things - expand the definition of "manufacturer" to mean: 💠A person in Canada who sells the cosmetic under their own name or a trademark, design, trade name, or other mark they own or control. 💠A person in Canada authorized to act on behalf…
Notified Bodies for IVD (EU vs CANADA)
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. Our exclusive webinar will cover: ✅Strategies for efficient regulatory compliance in both regions ✅Key differences between EU IVDR and Health Canada requirements ✅The role of Notified Bodies and how they impact IVD approvals 🎯 When: March 18th | 16:00-17:00 CET…
COSMOPROF 2025 – Bologna
Product launches and innovative solutions? Counting you in for Cosmoprof Bologna! Our goal is to assist your company in smoothly complying with global regulations and we will be there to support you. Why Meet Us at Cosmoprof Bologna? ✅ Expert insights on market access & compliance✅ Tailored strategies to accelerate approvals✅ Guidance on the latest…
IDS 2025 – Cologne
Bringing Your Dental Devices to Market? Join us at IDS, the world’s leading trade show for dental innovation! We’re here to help dental and medical device manufacturers easily navigate global regulations. Why Meet Us at IDS? ✅ Expert insights on market access & compliance✅ Tailored strategies to accelerate approvals✅ Guidance on the latest regulatory updates…
EUDAMED & National Registration: Navigating Compliance for Medical Devices
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…
UK Cosmetics Market: banned CMRs – April 2025
On October 3, 2024, the United Kingdom took a significant step toward tightening cosmetic safety by notifying the World Trade Organization (WTO) of a draft amendment to its GB Cosmetics Regulation. This update introduces 13 more chemicals to the growing list of banned substances, all of which are classified as carcinogenic, mutagenic, or reprotoxic (CMR).…
GPSR, VAT Compliance, and Customs: Essential Insights for Market Entry
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! Here’s what you…
Beauty Istanbul 2025 – Istanbul
Keen on Beauty Care? Let's meet at Beauty Istanbul, one of the largest cosmetics exhibitions worldwide! Our Mission? Helping cosmetics brands seamlessly adapt to global compliance standards.Why Meet Us at Beauty Istanbul?✅ Expert insights on market access & compliance✅ Tailored strategies to accelerate approvals✅ Guidance on the latest regulatory updatesLet’s connect and discuss how we can…
FDA U.S. Agent and Submissions
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: ✅Cybersecurity ✅U.S. Agent and Official Correspondent ✅Establishment Registration and Device Listing ✅Submissions (GUDID, 510k and others) 🎯 When: May 8 | 16:30-17:30 CET 📌 Where: Online…
IVDR Legacy Extension Deadline – May 2025
For in vitro diagnostic (IVD) manufacturers navigating the transition to the In Vitro Diagnostic Regulation (IVDR), a key deadline is approaching. The IVDR legacy extension applies only if manufacturers meet specific requirements: Submission of an application to a Notified Body ✅ Class D devices (high-risk IVDs that were self-certified under IVDD but now require a…
NYSCC 2025 – New York
Are Science and Beauty your work sectors? Then let's meet at NYSCC 2025, the premier event for personal care ingredients and formulations in North America! We are here to help your brand succeed in a globally regulated market.Why Meet Us at NYSCC?✅ Expert insights on market access & compliance✅ Tailored strategies to accelerate approvals✅ Guidance on…
FIME 2025 – Miami
Bringing Your Medical Devices to Market? Join us at FIME Miami, the largest international medical trade event in the USA!Our first goal? Supporting medical manufacturers in achieving regulatory compliance without the hassle. Why Meet Us at FIME? ✅ Expert insights on market access & compliance✅ Tailored strategies to accelerate approvals✅ Guidance on the latest regulatory…
GB/UK Post Market Surveillance: What You Need to Know
Navigating the evolving regulatory landscape in the UK can be complex, especially when it comes to Post Market Surveillance (PMS). Join 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,…
COSMOPROF 2025 – Las Vegas
Join us at Cosmoprof Las Vegas, the leading B2B beauty exhibition in the USA! We can help your company decode and comply with global regulations with confidence.What will you get in return?✅ Expert insights on market access & compliance✅ Tailored strategies to accelerate approvals✅ Guidance on the latest regulatory updatesLet’s talk! Set up a meeting in…
ADLM 2025 – Chicago
Scientific Meetings and Clinical Lab Expo? Looking forward to it! Join us and the global laboratory medicine community at ADML Chicago. Question about compliance? No need to worry, we are here to help you!Why Meet Us at ADML?✅ Expert insights on market access & compliance✅ Tailored strategies to accelerate approvals✅ Guidance on the latest regulatory updatesSet…
EUDAMED & Swissdamed Explained: Key Modules and Timelines for Medical Devices
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. Webinar highlights include: ✅What is public? ✅Code Usage ✅Timelines ✅Client Experiences to date 🎯 When: September 9 | 16:00-17:00 CET 📌 Where: Online | Zoho Webinars 🎬 Guests: Richard Houlihan (EirMed) and Georgios Mariolos (Obelis Group)
MEDICA 2025 – Düsseldorf
Heard about MEDICA? It is one of the largest medical B2B trade fairs in the world and we will be there to support you! Our goal is to assist your company in smoothly complying with global regulations. Why Meet Us at MEDICA? ✅ Expert insights on market access & compliance✅ Tailored strategies to accelerate approvals✅…