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Volume 15 Issue No. 22 |
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By MedTech Intelligence Staff Medtech companies can receive up to $300,000 for the adoption of advanced manufacturing technologies through the MDIC Advanced Manufacturing Clearing House. The program is designed to speed adoption and provide guidance for industry and the FDA on the most beneficial applications of advanced technologies. |
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| Featured Articles |
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MedDesign Leveraging AI & ML in MedTech: By Bob Bouthillier, Sunrise Labs There are several potential applications for machine learning and artificial intelligence in MedTech. In this article, we look at supervised ML with a classifier that learns to correlate IMU data patterns. |
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Soapbox Beyond EU MDR: By Monali Bhansali, Tata Elxsi The regulatory landscape for medical devices is rapidly evolving, catapulted most recently by European Union Medical Device Regulations (EU MDR). In this article, Monica Bhansali, Practice Lead of Regulatory Affairs at Tata Elxsi, highlights challenges and advancements in the MedTech regulatory landscape, and what the future has in store. |
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COMPLIMENTARY ON DEMAND WEBINAR |
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Sponsored By ETQ, LLC, part of Hexagon “A world without fear of cancer” is the corporate mission at Varian, a Siemens Healthineers company. To turn that vision into reality, the oncology care innovator prioritizes automated quality management across its imaging, treatment, and digital solutions. Follow Varian's quality journey from out-of-the-box standard QMS applications to a well-integrated enterprise platform that supports its data-driven product ecosystem with Srinivas Vindula, QMS Project Manager at Varian, and David Isaacson, VP of Product Marketing at ETQ. |
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AAMI and BSI Partner to Publish Guidance on Artificial Intelligence By MedTech Intelligence Staff AAMI and the British Standards Institute (BSI) have jointly published new guidance documents on performing risk management for machine learning or artificial intelligence incorporating medical devices. |
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What’s Happening in the UK and Switzerland By MedTech Intelligence Staff At the 2023 MedCon Conference in April, Michael Maier, VP of Strategic Regulatory and Quality at Veranex, and James Pink, Director of Medical at Element, provided updates on medical device regulation in Switzerland and the UK. |
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CALL FOR ABSTRACTS |
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MedTech Intelligence MedTech Abstracts Deadline: June 15 MedTech Intelligence and Axendia are requesting abstracts for content to be presented during our upcoming Conferences.
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| MedTech Library | |
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Sponsored By Veeva Medtech Terumo, global leader in medical technology, transforms to a unified, digital approach to manage global clinical trials and operations. Read this article to learn about the approach, processes, infrastructure changes, and impact on the business. |
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Sponsored By Arrow and Dell Technologies Learn the key considerations and best-fit solutions for healthcare transformation that optimize operations for providers and ensure better outcomes for patients. Discover how the Arrow Electronics and Dell Technologies OEM Solutions portfolio can match any healthcare need. |
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Sponsored By Rimsys The 2023 MedTech Regulatory Performance Report provides insights and process benchmarks from a survey of 200 medtech regulatory professionals across North America and Europe. The report explores regulatory staffing and team size, workload and average times to complete regulatory projects, compliance issues and costs, and the role of technology and digital transformation. |
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Drive Healthcare Transformation with Enterprise-Level Infrastructure
2023 MedTech Regulatory Performance Report
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| Upcoming Events & Webinars |
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June 6, 2023 - 10:00am EDT/4:00pm CEST Mastering EU MDR: |
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June 8, 2023 - 10:00am EDT Not All Medical Products Are Created Equal. |
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MedTech Intelligence 2023 Washington DC Conferences More info at MedTechIntelligence.com November 7-8 November 8-9 November 13-14 |
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