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Medical devices are different to pharmaceuticals in the Health Technology Assessment process.

作者信息

Ferguson Michael

机构信息

Boston Scientific, Natick, MA, USA.

出版信息

J Comp Eff Res. 2014 May;3(3):217-9. doi: 10.2217/cer.14.17.

DOI:10.2217/cer.14.17
PMID:24969145
Abstract
摘要

相似文献

1
Medical devices are different to pharmaceuticals in the Health Technology Assessment process.在卫生技术评估过程中，医疗设备与药品有所不同。
J Comp Eff Res. 2014 May;3(3):217-9. doi: 10.2217/cer.14.17.
2
Technology assessment of medical devices at the Center for Devices and Radiological Health.设备与放射健康中心对医疗设备的技术评估。
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3
The limited state of technology assessment for medical devices: facing the issues.医疗器械技术评估的有限状态：面对相关问题。
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4
Health technology assessment for medical devices in Europe. What must be considered.欧洲医疗器械的卫生技术评估。必须考虑的因素。
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5
Evolving reimbursement and pricing policies for devices in Europe and the United States should encourage greater value.在欧美，不断演变的设备报销和定价政策应鼓励创造更高的价值。
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The truth behind "made in Europe" labels on medical devices.医疗器械上“欧洲制造”标签背后的真相。
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An EU-wide approach to HTA: An irrelevant development or an opportunity not to be missed?欧盟范围内的 HTA 方法：不相关的发展还是不容错过的机会？
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8
Medical device technology user fees.
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Health technology assessment from a Canadian device industry perspective.从加拿大设备行业视角看卫生技术评估。
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[An exploratory discussion on biological evaluation and risks for medical devices].[关于医疗器械生物学评价及风险的探索性讨论]
Zhongguo Yi Liao Qi Xie Za Zhi. 2006 Sep;30(5):386-7, 382.

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Critical Review of European Health-Economic Guidelines for the Health Technology Assessment of Medical Devices.
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Evaluating the Safety Profile of Non-Active Implantable Medical Devices Compared with Medicines.评估非有源植入式医疗器械与药物相比的安全性概况。
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