Element RegNav’s Post

🟣 Is your medical device being overlooked? Do you want to rapidly increase the uptake of your device in 2024 with clear, consistent communication that’s understood in seconds?    If so, between now and the 5th of February, I am offering 7 free messaging audits to medical device companies who feel their device isn’t gaining the traction it deserves. If this is of interest, send me a direct message, and I can send you more details of what’s included.    #MedTech #MedicalDevices  

Navigating the complexities of change control in the medical device industry can be challenging. That is why we have distilled key insights and best practices into a bite-sized video that packs a punch! 🎥💡 #MedicalDevices #ChangeControl #HealthcareInnovation #RegulatoryCompliance #MedTech

🔍 𝐍𝐞𝐰 𝐄𝐩𝐢𝐬𝐨𝐝𝐞 𝐀𝐥𝐞𝐫𝐭! 🎥 In our latest video, we’re demystifying some key medical device terms you need to know: ◼ 𝘊𝘰𝘮𝘱𝘢𝘵𝘪𝘣𝘪𝘭𝘪𝘵𝘺 ◼ 𝘐𝘯𝘵𝘦𝘳𝘰𝘱𝘦𝘳𝘢𝘣𝘪𝘭𝘪𝘵𝘺 ◼ 𝘔𝘢𝘬𝘪𝘯𝘨 𝘈𝘷𝘢𝘪𝘭𝘢𝘣𝘭𝘦 𝘰𝘯 𝘵𝘩𝘦 𝘔𝘢𝘳𝘬𝘦𝘵 ◼ 𝘗𝘭𝘢𝘤𝘪𝘯𝘨 𝘰𝘯 𝘵𝘩𝘦 𝘔𝘢𝘳𝘬𝘦 ◼ 𝘗𝘶𝘵𝘵𝘪𝘯𝘨 𝘪𝘯𝘵𝘰 𝘚𝘦𝘳𝘷𝘪𝘤𝘦 Join us as we break down these concepts in simple terms, so you can navigate the medical device world with confidence. 🌟 Watch the full episode #MedicalDevices #RegulatoryAffairs #TechSimplified #MedicalDeviceRegulation #LinkedInLearning #MedicalDevices #RegulatoryAffairs #TechSimplified #MedicalDeviceRegulation #LinkedInLearning #MedTech #HealthcareInnovation #DeviceCompliance #EURegulations #MedicalDeviceIndustry #TechTerms #InnovationInHealthcare

🚨 Navigating the Compliance Maze in Medical Device Development 🚨 Bringing a medical device to market is no small feat—regulatory challenges can be a huge hurdle! 🛠️ Innovengg breaks down the key compliance issues and offers expert insights on how to overcome them in our latest article. 📑 🔍 Stay ahead in the medical device industry with the right strategies and knowledge! Read more here: https://lnkd.in/geJweaYu #MedicalDevices #RegulatoryCompliance #Innovengg #MedicalTechnology #InnovationInHealth

🚀 New Read: Deciphering Device Longevity: A Comprehensive Analysis of Team-NB's Position on Medical Device Lifetime We're pleased to announce our latest Whitepaper, providing an insightful exploration into a notable topic in the medical device industry: understanding the lifetime and durability of these vital tools. Our new blog post unpacks the latest Team-NB's Position Paper from 15 December 2023, offering crucial perspectives for professionals across the healthcare and regulatory landscape. 🌟 What you'll uncover: A review at the complexities surrounding 'medical device lifetime' and its implications within the MDR framework. Insights and recommendations for manufacturers to maintain device safety and effectiveness over time. For professionals in manufacturing, healthcare, or regulation, this article provides practical perspectives to inform your strategies on medical device longevity. 👉 Dive into the full analysis here: https://lnkd.in/eg2wsYia #MedicalDevices #HealthcareInnovation #PatientSafety #MedicalTechnology #RegulatoryAffairs #TeamNB #DeviceDurability #BlogPost #CeMarking #NotifiedBody

I am Happy to share that i have successfully completed the US Medical Device reporting course from .VigiServe Foundation This course helped me to know more about Medical Device reporting guidelines in the US market. #medicaldevice #regulatoryaffairs

Looking for insights to bring your medical devices to market efficiently? Download 👇 this whitepaper to avoid pitfalls and missteps along the way, written by Element RegNav medical device compliance experts. Nicole Small Michael Kipping James Pink https://ow.ly/Y9X850SlTZm #MedicalDevices #MedicalTechnology #RegulatoryCompliance #MedicalDeviceDevelopment #Whitepaper #RegNav #ElementRegNav

🌐 Have you visited our website yet? We’ve made some exciting updates and added new resources to help you stay informed and ahead in the medical device industry. ➡️https://lnkd.in/d3vwJzkM 📽️ Watch the video below to learn more about our services, recent blog posts, and how we can support your journey in medical device compliance and innovation. #medicaldevices #MDR #medicaldeviceregulation #medizinprodukte #medizinprodukteverordnung #Regulation #Compliance #MDCG #MedTech #Healthcare #medxteam 

The Global Medical Device Nomenclature (GMDN) codes are a comprehensive and standardized system used to identify and classify medical devices. GMDN codes are developed and maintained by the GMDN Agency, with the aim of providing a universal language that simplifies the regulatory and communication processes within the healthcare industry. Read the blog here: https://lnkd.in/ezYDWvrN

Team-NB has published the position paper "Medical Device Lifetime. This document addresses Lifetime with the objective of considering different device types within a medical device's lifetime in terms of safe and effective use. #medicaldevices #regulatoryaffairs #regulatoryglobe