Using medical registries: Switzerland’s implant registry SIRIS as a successful model

Nicole Steck, M. Zwahlen, A. Spoerri
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Abstract

With the increasing use of implantable medical devices, registries are critical for conducting post-market surveillance and identifying long-term safety risks. Switzerland’s national implant registry SIRIS is an outstanding example of the benefits a well-managed registry can provide to different players in healthcare. The SIRIS registry also illustrates how to ensure high-quality registry data.
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使用医疗登记:瑞士的植入物登记SIRIS是一个成功的模式
随着植入式医疗器械的使用越来越多,注册对于进行上市后监测和确定长期安全风险至关重要。瑞士的国家植入物注册中心SIRIS是一个很好的例子,说明管理良好的注册中心可以为医疗保健领域的不同参与者提供好处。SIRIS注册表还说明了如何确保高质量的注册表数据。
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The PES-SLEEP project: A practical approach to the categorisation challenge for studies with medical devices Challenges facing Switzerland’s medical technology industry following the 2021 changes to medical device legislation Swissmedic’s experience with the regulatory changes for clinical investigations with medical devices implemented in 2021 Patient input into medical device development: A missed opportunity Regulatory developments in the medical devices sector: A long and difficult journey
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