Orion Health’s Post

As a leader in providing cutting-edge medical solutions, QISH MEDICAL TRADING is excited to showcase our latest innovations and partnerships that are shaping the future of healthcare. We’re proud to be part of an event that brings together global experts, pioneers, and industry leaders to share knowledge, explore new technologies, and collaborate for better patient outcomes. 🎥 Watch our exclusive videos from the event, where we highlight: Our state-of-the-art medical informatics and solutions Engaging demos and live showcases Key insights from our team of experts Discussions on the future of healthcare and medical technology 👉 Don't miss out on seeing what’s new in healthcare and how QISH MEDICAL TRADING is helping drive progress. #QISHMedicalTrading #Medicare2024 #HealthcareInnovation #Exhibitor #MedTech #MedicalDevices #Qatar #FutureOfHealthcare #HealthTech #PatientCare #GlobalHealthcare #MedicareExhibition

In an era where healthcare and technology are increasingly intertwined, Software as a Medical Device (SaMD) stands at the cutting edge of patient care. From diagnostics to remote monitoring, SaMD opens new doors for real-time insights and personalized treatment options. At Innovenn, our team brings deep expertise in navigating the unique regulatory, clinical, and usability challenges that come with SaMD development. Designing software to operate reliably within critical healthcare settings requires not only advanced technical knowledge, but also a clear understanding of compliance and patient safety. By working closely with clients from ideation through regulatory approval, we help transform innovative ideas into compliant, patient-focused software solutions that truly make a difference. Find out how we can support you in the SaMD regulatory process: https://lnkd.in/gR8RAhAN #SaMD #MedicalDeviceConsulting #HealthcareInnovation #PatientSafety #DigitalHealth

🚀 NAMSA BLOG! 🚀 The FDA, Health Canada, and MHRA have jointly released the "Transparency of Machine Learning-Enabled Medical Devices: Guiding Principles." This new publication builds upon the 2021 Good Machine Learning Practice (GMLP) principles, emphasizing the importance of transparency in MLMDs. 🧠 Key Highlights: ◾️Principle 7: Focus on the performance of the human-AI team. ◾️Principle 9: Clear, essential information for users. Transparency in MLMDs ensures informed choices, manages risks, and promotes equity by revealing biases. 🔍 Explore the six transparency principles: the audience, importance, relevant info, placement, timing, and human-centered design support. 📢 Read the full blog by Monica R. Montanez, Principal Strategy Consultant, to learn more about these guiding principles and their impact on the medical device industry 👉 https://lnkd.in/gvnCtM6w #MedicalDevices #MachineLearning #Transparency #HealthcareInnovation #NAMSAKnows

Explore the power of post-market clinical surveys to elevate device safety and performance. In this blog, Prem Narayan Pandey highlights strategies that drive continuous improvement, compliance, and innovation in the medical technology field. Read the blog https://lnkd.in/d99NcWzz #devicesafety #pmcfsurveys #pmcf #eumdr #clinicalregulatory #medicaldevice #medtech

🚀 NAMSA BLOG! 🚀 The FDA, Health Canada, and MHRA have jointly released the "Transparency of Machine Learning-Enabled Medical Devices: Guiding Principles." This new publication builds upon the 2021 Good Machine Learning Practice (GMLP) principles, emphasizing the importance of transparency in MLMDs. 🧠 Key Highlights: ◾️Principle 7: Focus on the performance of the human-AI team. ◾️Principle 9: Clear, essential information for users. Transparency in MLMDs ensures informed choices, manages risks, and promotes equity by revealing biases. 🔍 Explore the six transparency principles: the audience, importance, relevant info, placement, timing, and human-centered design support. 📢 Read the full blog by Monica R. Montanez, Principal Strategy Consultant, to learn more about these guiding principles and their impact on the medical device industry 👉 https://lnkd.in/gvnCtM6w #MedicalDevices #MachineLearning #Transparency #HealthcareInnovation #NAMSAKnows

Stay informed and ahead of regulatory challenges with the Market Pathways MedTech Regulatory Article Pack. As regulations and market access strategies rapidly evolve, it's crucial for regulatory professionals to stay updated. The Market Pathways Article Pack offers a first-of-its-kind resource, designed to help you and your team navigate these changes and implement effective medtech strategies. Explore key topics including but not limited to: • AI integration in MedTech • Global health policy shifts • Innovation and compliance in the medical device space #Ad Download for free here 👉 https://bit.ly/4elfsRg #MedTech #RegulatoryAffairs #MarketAccess #Innovation #RAPS #MedicalDevices

Stay informed and ahead of regulatory challenges with the Market Pathways MedTech Regulatory Article Pack. As regulations and market access strategies rapidly evolve, it's crucial for regulatory professionals to stay updated. The Market Pathways Article Pack offers a first-of-its-kind resource, designed to help you and your team navigate these changes and implement effective medtech strategies. Explore key topics including but not limited to: • AI integration in MedTech • Global health policy shifts • Innovation and compliance in the medical device space #Ad Download for free here 👉 https://bit.ly/4elfsRg #MedTech #RegulatoryAffairs #MarketAccess #Innovation #RAPS #MedicalDevices

🚀 Exciting news! Introducing CTOps by Mushroom Solutions - the ultimate solution to revolutionize your clinical trials. Improve accuracy, enhance participant engagement, and streamline workflows with ease. Say hello to the future of medical research! More info Visit: https://lnkd.in/g_ArYjkm #CTOps #ClinicalTrials #Innovation #ClinicalTrials #MedicalResearch #Innovation #Efficiency #Compliance

The European Association of Medical Devices Notified Bodies (Team-NB) has unveiled its High-Level Strategy Position Paper outlining bold steps to harmonize, simplify, and innovate within the regulatory framework of #MedicalDevices and #IVDDiagnostics. Here's what stands out: ✅ Strengthening Notified Bodies: 42 organizations with 5,200+ professionals are championing better governance, transparency, and risk-proportionate approaches across the EU. ✅ Empowering SMEs: Team-NB emphasizes support for small and medium enterprises (SMEs), which represent 77% of their clientele, proposing enhanced EU financial aid for certification processes. ✅ Driving Harmonization: Proposals to streamline processes through unified technical documentation standards, better governance via MDCG structures, and addressing gaps in clinical data for special devices. ✅ Leveraging Digital Transformation: Introducing AI-driven efficiencies and data-centric processes to minimize administrative burdens while ensuring patient safety. 💡Follow us Biomedista Consulting #MedTech #InnovationInHealth #Regulations #EUHealthcare #PatientSafety #TeamNB

🚀 Blog Alert: FDA's Guidance on Digital Health Technologies! 💡 Discover the latest insights from the FDA's Industry Guidance on Digital Health Technologies for Remote Data Acquisition in Clinical Investigations. 🌐 Key Takeaways: 👉 Definition of Digital Health Technologies (DHT) and their role in remote data acquisition 📊 Examples of DHT applications in clinical trials 🛠️ Design control requirements for DHTs used as medical devices 🔍 Selection criteria for choosing DHTs in clinical investigations Ready to delve into the details? Read the full guidance document here: https://lnkd.in/eekRZVVb 🌐 And did you know? NAMSA offers support for qualification proposals to CDRH's MDDT Qualification Program! #FDA #DigitalHealth #ClinicalTrials #NAMSAInsights #MedTech #NAMSAKnows