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Volume 13 Issue No. 19 |
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By Dr. Abtin Rad, TÜV SÜD Product Service GmbH A review of common risks and pitfalls of incorporating artificial intelligence in medical devices and an overview of the regulatory framework. |
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Soapbox Does the Long-Term Future of Telehealth Mean Lower Healthcare Costs? By Mary Jo Condon, Freedman Healthcare To better understand the future of telehealth, it is important to understand what the costs look like over time and whether telehealth offers advantages in cutting healthcare costs overall. |
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Incidence of Severe Cardiovascular Conditions Fuels Cardiac Arrhythmia Monitoring Devices Industry By Saloni Walimbe, Global Market Insights, Inc. The pandemic has ushered in a novel era of cardiac health management, with remote patient monitoring at its forefront. |
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By MedTech Intelligence Staff Other industries are already seeing the benefits of more holistic and interchangeable data/document management in enabling process optimization and transformation, but until now the life sciences industry has been slower to understand the benefits to be gained from a more fluid approach to managing information in all its formats. |
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MEDdesign COVID-19 Pushes Technology to Facilitate Hybrid Patient Care By Erik Vanderlip, M.D., ZOOM+Care Increased access to care is a vital part of the vision to innovate the delivery of healthcare. |
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SPONSORED RESOURCE |
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Sponsored By Drishti Technologies, Inc. The video revolution has come to medical device assembly. Here are the top six ways leading Class II/III device manufacturers are using video to transform the effectiveness of everyone on and around the line — including the line operators themselves. |
Top 6 uses for video on medical device assembly lines
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| MedTech Library | |
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Sponsored By S3 Connected Health Connectivity is now a must when designing or redesigning in-hospital medical equipment. Data insights collected on connected medical devices can bring many benefits for vendors, healthcare providers, and patients; from improving healthcare outcomes to reducing the cost of care and device maintenance. |
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Top 6 uses for video on medical device assembly lines Sponsored By Drishti Technologies, Inc. |
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How CPQ Helps Your Sales Team Drive Revenue and Increase Profits Sponsored By Experlogix, LLC |
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Experlogix CPQ for the Medical & Mobility Industry Sponsored By Experlogix, LLC |
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The Business Value of Cybersecurity in MedTech Sponsored By Irdeto |
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MDR Documentation Submissions: Best Practices Guidelines Sponsored By bsi. |
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Explaining IVD Classification Issues Sponsored By bsi. |
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How medical device companies can create end-to-end connectivity for in-hospital equipment|
NOW ON-DEMAND! |
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The European In Vitro Diagnostic Regulation (EU IVDR) will profoundly affect the global diagnostics market, requiring new procedures, evidence development, documentation, organizational structures, data management, reporting, and a reassessment of legacy portfolios. Preparation will involve strategic thinking and buy-in at the highest levels. Implementation of IVDR is scheduled for May 2022, with no indication that it will be deferred. For those who have not already begun planning for the change, it is urgent to begin now or face exclusion from the European market. Recorded March 30, 2021: EU IVDR Introduction Recorded April 6, 2021: Quality Processes and Documentation Recorded April 13, 2021: Clinical Evidence & Surveillance Recorded April 20, 2021: Supply Chain Management: Economic Operators, UDI, and Labeling Recorded April 27, 2021: Strategy and Planning |
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