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Regulation of Medical Devices

The ANNALS of the American Academy of Political and Social Science, 1972
The regulation of medical devices presents unique difficulties because of the breadth and complexity of the industry. Experts agree that increased federal control is essential to adequately protect the public, because of the serious loopholes in the Food and Drug Administration's cur rent premarketing controls.
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Medical Device Regulations Update

2021
• Introduction Mark Turner, Chair of the HSE Medical Device Regulations Steering Group • HPRA Perspective Andrew Dullea , Regulatory & Policy Assessor | Medical Devices, Health Products Regulatory Authority • HSE Perspective Ger Flynn, National Clinical Lead for Medical Devices • Key Messages for Hospitals Ciaran Browne, Acute Operations • Q & A ...
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Medical Device Development: Innovation versus Regulation

The Annals of Thoracic Surgery, 1980
Innovation in the development of medical devices has been an important factor in the practive of health care in the United States. However, in a climate of increasing federal regulation, concern is expressed that such regulation can inhibit scientific creativity in the medical device industry.
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Medical device regulations

2020
Mounika Gudeppu   +3 more
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Australian Medical Device Regulations: An Overview

2018
In Australia, medical devices are regulated by the Therapeutic Goods Administration (TGA). The Australian medical device regulatory requirements, which were implemented in 2002, are largely based on the European Council Medical Device Directive (MDD) 93/42/ European Economic Community (EEC).
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Integrative oncology: Addressing the global challenges of cancer prevention and treatment

Ca-A Cancer Journal for Clinicians, 2022
Jun J Mao,, Msce   +2 more
exaly  

Medical device regulation in Australia

Medical Journal of Australia, 1992
F J, Morgan, M J, Brown
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Medical Devices Regulation

2016
Teresa Pankiewicz   +5 more
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