Learn how to plan and prepare your team and data for managing UDI data to meet the EUDAMED submissions deadline. Join our webinar on July 2nd to hear from industry experts. Learn more and register here: https://bit.ly/4eBA8ow #LifeSciences #MedicalDevices #EUDAMED #UDI #MedicalDevicesRegulation
USDM Life Sciences’ Post
More Relevant Posts
-
I do highly recommend to join our upcoming webinar with our expert Jay Crowley and Lionel Tussau from our partner BAYARD on UDI data management and submission to EUDAMED to meet most recent EU requirements and deadlines. If you can’t join but interested in the subject and looking for help or a solution, feel free reaching out to me directly bis LinkedIn. #UDI #EUDAMED #MEDICALDEVICES
Learn how to plan and prepare your team and data for managing UDI data to meet the EUDAMED submissions deadline. Join our webinar on July 2nd to hear from industry experts. Learn more and register here: https://bit.ly/4eBA8ow #LifeSciences #MedicalDevices #EUDAMED #UDI #MedicalDevicesRegulation
To view or add a comment, sign in
-
-
Last chance to join the webinar tomorrow and learn how to prepare your team and data for managing UDI data to meet the EUDAMED submissions deadline. Register now: https://bit.ly/4eBA8ow #LifeSciences #MedicalDevices #EUDAMED #UDI #MedicalDevicesRegulation
To view or add a comment, sign in
-
-
Join our webinar on July 2nd to learn how to plan and prepare your team and data for managing UDI data to meet the EUDAMED submissions deadline. Learn more and register here: https://bit.ly/4eBA8ow #LifeSciences #MedicalDevices #EUDAMED #UDI #MedicalDevicesRegulation
To view or add a comment, sign in
-
-
📢 NEW WEBINAR ABOUT EUDAMED : THE PATHWAY TO THE COMPLIANCE 🌟 In June, TEAM-PRRC organizes 2 webinars about EUDAMED. Join us to our next webinar about EUDAMED presented by Stéphane Ancel , Business Manager of ACKOMAS on June 4th, at 5.00 pm CET. This webinar will be moderated by Ajda Mihelčič from Obelis. There are many questions about EUDAMED and how to register its devices. To know more, don’t miss this webinar. The webinar is open to all. To register click here: https://lnkd.in/eypetNaY Then, another webinar will be presented by Ajda Mihelčič about the latest updates regarding EUDAMED on June 27th. Stay tuned for the registration. We look forward to seeing you. #MDR #IVDR #PRRC #medicaldevice #regulation #eudamed #registration #UDI
To view or add a comment, sign in
-
-
Last 1 week to join us to our next webinar about EUDAMED : THE PATHWAY TO THE COMPLIANCE. In June, TEAM-PRRC organizes 2 webinars about EUDAMED. Join us to our next webinar about EUDAMED presented by Stéphane Ancel , Business Manager of ACKOMAS on June 4th, at 5.00 pm CET. This webinar will be moderated by Ajda Mihelčič from Obelis Group. There are many questions about EUDAMED and how to register its devices. To know more, don’t miss this webinar. The webinar is open to all. To register click here: https://lnkd.in/eypetNaY Then, another webinar will be presented by Ajda Mihelčič about the latest updates regarding EUDAMED on June 27th. Stay tuned for the registration. We look forward to seeing you. #MDR #IVDR #PRRC #medicaldevice #regulation #eudamed #registration #UDI
To view or add a comment, sign in
-
-
Understanding and embracing the EUDAMED implementation plan is important. EUDAMED, the European Databank on Medical Devices, is being placed as a pivotal tool. 🚀 EUDAMED Milestones: The journey commenced with the activation of the Actor Registration module in December 2020. Subsequently, the UDI/Device Registration and Notified Bodies and Certificates modules followed suit in October 2021, marking significant progress. 🎯 What's on the Horizon?: Anticipate the activation of three vital modules: Clinical Investigations and Performance Studies, Vigilance and Post-Market Surveillance, and Market Surveillance, upon EUDAMED's full operational status. While EUDAMED usage remains voluntary for now, it will transition to a mandatory tool for all Medical Device manufacturers once all six modules are fully functional. ⏳ Preparation for Compliance: Acquaint yourself with the available modules to streamline compliance processes. Stay updated on the progress of EUDAMED implementation and be ready for the mandatory transition. 🌐 Empowering Healthcare Together: The successful integration of EUDAMED is a collaborative effort toward enhanced healthcare and safety. Let's embrace this transformation and ensure we're well-prepared for a compliant future: https://loom.ly/KUoY6AA #MedicalDeviceManufacturers #EUDAMED #EURegulations #HealthcareInnovation #RegulatoryCompliance #StayInformed #MedicalDevices #EUMarket #HealthTech #EUCompliance #HealthcareSafety #MedTech
To view or add a comment, sign in
-
CLIN-r+ are delighted to announce their participation at the SurgiTech 2024 summit on supporting innovation across the surgical pathway and are looking forward to seeing you there on FRIDAY!! Details on the Panel discussion 'Regulatory strategy to ensure your UK and EU market access.' so far…. Common mistakes in the MedTech sector can delay market entry and reduce company value. Our expert panel will explore these pitfalls, offering insights to keep you ahead. By avoiding these blunders, start-ups can maximise investments, speed up market entry, and enhance their valuation. Key discussions include: 👉Setting out with a clear roadmap. 👉What the EU and UK market offers and why the difficulty in producing a Technical Document for this jurisdiction can give you an international advantage and save costs in entering the USA, AU and another markets? 👉Designing a Clinical Development Plan to boost commercial results and company value. Whilst you're there, you are also welcome to make an appointment with us in advance to discuss your regulatory or clinical affairs needs to obtain your MDR CE mark. We are offering clients a free 40-minute consultation (at the event or virtually) to discuss your most pressing EU MDR Clinical Regulatory questions. BOOK NOW! https://loom.ly/-K2iFVc More details and tickets to the event can be found here: https://loom.ly/2a98ylE
SurgiTech 2024 - complementary regulatory consultation - CLIN-r+ consultancy
calendly.com
To view or add a comment, sign in
-
An insightful dive into the FDA's new regulations on Laboratory Developed Tests (LDTs), highlighting 𝘁𝗵𝗲 𝗽𝗼𝘁𝗲𝗻𝘁𝗶𝗮𝗹 𝗶𝗺𝗽𝗮𝗰𝘁 𝗼𝗻 𝘁𝗵𝗲 𝗺𝗲𝗱𝘁𝗲𝗰𝗵 𝗶𝗻𝗱𝘂𝘀𝘁𝗿𝘆. This article effectively captures 𝘁𝗵𝗲 𝗸𝗲𝘆 𝗽𝗼𝗶𝗻𝘁𝘀 𝗼𝗳 𝘁𝗵𝗲 𝗳𝗶𝗻𝗮𝗹 𝗿𝘂𝗹𝗲, 𝘀𝗵𝗲𝗱𝗱𝗶𝗻𝗴 𝗹𝗶𝗴𝗵𝘁 𝗼𝗻 𝗵𝗼𝘄 𝗶𝘁 𝘄𝗶𝗹𝗹 𝘀𝗵𝗮𝗽𝗲 𝘁𝗵𝗲 𝗹𝗮𝗻𝗱𝘀𝗰𝗮𝗽𝗲 𝗳𝗼𝗿 𝗱𝗶𝗮𝗴𝗻𝗼𝘀𝘁𝗶𝗰 𝘁𝗲𝘀𝘁𝗶𝗻𝗴. With a clear breakdown of the regulatory changes and expert analysis, it's a must-read for professionals navigating this evolving regulatory environment - https://lnkd.in/ddude-i8 #FDA #MedicalTechnology #LDTs #Regulation #LabTesting #Healthcare #MedicalDevices #MedTech #HealthTech #MedTechTrends #VivicaLIMS #LifeDataLab https://about.vivica.us https://lifedl.net
To view or add a comment, sign in
-
-
🗓️ Just 2 weeks until the DIA Global Labeling Conference! Excitement is building as we prepare to showcase the transformative impact of AI on ePI conversions. Join us to explore the future of patient safety through interoperable healthcare. ➡️ https://lnkd.in/euSG2HDa #PatientCentricity #MedicationEducation #Pharma #LifeSciences #StructuredContent #Compliance #ContentCompliance #Labeling24
To view or add a comment, sign in
-
-
📣December 2023📣 MDCG 2021-6 Rev. 1 Regulation (EU) 2017/745 – Questions & Answers regarding clinical investigation. Source: https://lnkd.in/dPayWe7D #eudamed #medtech #medicaldevices #regulatoryaffairs #regulatorycompliance #EUDAMED
To view or add a comment, sign in