TÜV SÜD - Healthcare & Medical Devices

🚀Come and meet Stefano Bolletta, Europe Sales Manager at TÜV SÜD, at the AI for Health Summit in Paris, happening next week! 📅 Date: 21 November 2024 📍 Location: Station F, Paris, France Click here to book to meeting 👉http://spkl.io/6042fpqsC Date: 21 November 2024 #TUVSUD #medicaldevices #AI

Don't miss out on the webinar! Are you prepared to tackle the evolving landscape of PFAS regulations? Join our experts from TÜV SÜD in Tata Elxsis' webinar as they break down the latest scientific findings and delve into the multifaceted world of PFAS in medical devices. This event will bring together a wide variety of experts to explore the latest scientific findings on PFAS, and how the research is becoming a reality. 💡 Key topics: ✔️ Forecasting regulatory shifts ✔️ Transition strategies to replace PFAS ✔️ Supply chain adjustments 🗓️ Date: November 19, 2024 🕘 Time: 9:00 am EST | 3:00 pm CET Register now! ➡️http://spkl.io/6049fpqJb #PFAS #Webinar #MedicalDevices #Sustainability

🔍 How protected is your medical device from cyber threats? Are you confident your data is safe? 📢 Protecting medical devices from digital threats is essential today. Learn the best practices in our free webinar on 22 November at 11:00 a.m. Don’t miss this chance to engage with medical device cybersecurity experts! Sign up now: http://spkl.io/6040fprxs #cybersecurity #TUVSUD #medicaldevice

🔬 ISO 10993 compliance is crucial for medical devices that come into contact with the human body. TUV SUD offers a comprehensive range of ISO 17025 and GLP-compliant testing services to ensure your products meet global standards. Download the brochure now at 👉 http://spkl.io/6044fTQks #biocompatibility #BiocompatibilityTesting #TUVSUD

🚀 Join the "Medical Update" event: MDR (EU) Regulation 2017/745 - Key Changes This is a must-attend event for medical device manufacturers. In today's complex regulatory landscape, staying informed about European regulations is critical. ❓ What planning strategies can help ensure a smooth and efficient process for modifying medical devices? Discover the answers by registering for the Medical Update event, where we will delve into this and other vital industry topics. Don’t miss this chance to get the crucial insights needed to ensure your products' compliance and safety! 📅 Date: 3 December (English edition) 📍 Format: Online and In-person Sign up now to secure your spot: http://spkl.io/6048fTQNu #MedicalUpdate #medicaldevices #Compliance #NotifiedBody

Come meet Edoardo Pozzi at MEDICA, Internation Trade Fair for Medical Technology & Healthcare 🚀 Edoardo, Sales Europe at TÜV SÜD, will be participating at MEDICA Trade Fair on 11-14 November, 2024 in Düsseldorf, Germany (Hall 8a / P27) 📧 Email him at [email protected] to book your appointment today!

🔍 Continuing our series to understanding the common challenges encountered during medical device testing, we want to know about your experience in packaging testing 📦

🚀 Exciting News! 🚀 We are thrilled to announce that we've officially been recognized by the South African Health Products Regulatory Authority (SAHPRA) as a conformity assessment body for issuing ISO 13485 certificates in South Africa! 🎉 In addition, TÜV SÜD is also accredited by Singapore Accreditation Council in Singapore to facilitate the certification of companies to SAC ISO 13485. 🌍 Click on the link below to find out more: http://spkl.io/6047fRC2f #ISO13485 #TUVSUD #medicaldevices

Are you prepared to tackle the evolving landscape of PFAS regulations? Join our experts from TÜV SÜD in Tata Elxsis' on-demand webinar as they break down the latest scientific findings and delve into the multifaceted world of PFAS in medical devices. 💡 Key topics: ✔️ Forecasting regulatory shifts ✔️ Transition strategies to replace PFAS ✔️ Supply chain adjustments Watch now! ➡️http://spkl.io/6047frBBV #PFAS #Webinar #MedicalDevices #Sustainability