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2020年欧洲数字健康创新途径展望报告-EIT Health(40页英文版).pdf

上传人: Me****y 编号:19422 2020-09-22 40页 4.01MB

1、EUROPEAN REPORT 2020 Round Table Series: Recommendations Future-proofing Europes digital health innovation pathway Start reading Table of contents Conclusions Round Table meeting feedback The purpose of the EIT Health Think Tank Round Table series Round Table series 2019 overview The purpose of the

2、EIT Health Think Tank Round Table series The EIT Health Think Tank is a forum of experts and thought leaders collaborating to shape the future of healthcare in Europe. This could ultimately ensure patients and citizens have access to healthcare innovations that could potentially transform outcomes.

3、Each year a topic high on the European health agenda is selected for deeper exploration in meetings, which take place at Round Tables across the EIT Health regions. These draw on the experience, knowledge and skills of experts from EIT Healths broader community. These regional meetings focus on spec

4、ific local needs, opportunities and barriers, while also identifying successful solutions and examples of best practice that could be replicated at a European level. The Think Tank aims to ensure that expert recommendations are translated into realistic and meaningful outcomes, accelerating innovati

5、on in health for the benefit of all European citizens - so they are able to live longer, healthier lives. Round Table series 2019 Overview THINK TANK TOPIC For the 2019 Think Tank Round Table Series, participants discussed the topic Optimising Innovation Pathways: Future Proofing for Success. The in

6、novation pathway describes the progress healthcare innovations make from a need and an idea to a product or service on the market that is adopted, or even becomes the standard of care. For traditional medicinal products and devices, the steps of the innovation pathway in EU member states are relativ

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本文主要讨论了如何优化欧洲数字健康创新路径。主要观点包括: 1. 数字健康创新需要新的方法,以适应其快速迭代和集成服务特性。 2. 需要明确数字健康技术的监管要求,并让所有利益相关者参与其中。 3. 需要开发数字健康技术的卫生技术评估(HTA)证据要求,并让所有利益相关者参与其中。 4. 需要协调监管和HTA过程及要求,并向所有利益相关者传达。 5. 需要实施欧洲范围内对数字健康技术的HTA,以实现可持续的欧盟合作。 6. 需要“过程标准”而非“产品标准”来适应数字健康技术持续创新和证据生成的需求。 7. 需要能够监管和评估整体系统和方法,而不仅仅是单个产品。 8. 需要一个持续评估、监测(类似于上市后药品监测)和必要时淘汰过时技术的流程。
欧洲数字健康创新路径如何优化? 数字健康技术面临哪些挑战? 如何确保数字健康创新惠及公民?
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