منابع مشابه
How are medical devices regulated in the European Union?
The Medical Technology Evaluation Programme (MTEP) within the National Institute for Health and Clinical Excellence (NICE) was set up in 2009; this is a programme focusing specifically on the selection and evaluation of new or innovative medical technologies (including devices and diagnostics). One of the requirements to enable a product to be evaluated by the MTEP is that the device is CE mark...
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Implantable medical devices— such as insulin pumps, cardiac pacemakers, and cardiac defibrillators—have become increasingly popular since being introduced about 50 years ago. In the US alone, 2.6 million people rely on IMDs. An increasing number of today’s devices are equipped with wireless technology enabling, for example, remote checks by healthcare workers. “Patients often receive at-home, b...
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ژورنال
عنوان ژورنال: Research Ethics
سال: 2012
ISSN: 1747-0161,2047-6094
DOI: 10.1177/1747016112440391