Medical Imaging and FDA Regulatory Pathway for Radiology devices

Sunil Aggarwal and Somya Aggarwal
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Somya Aggarwal: Independent scholars, New York, USA

Current Trends in Clinical & Medical Imaging, 2016, vol. 1, issue 1, 1-2

Abstract: The medical imaging arena is fast developing and changing from the days of simple X-rays to advanced MRI imaging. Radiological imaging is very important in the targeted, clinical diagnosis and management of patients, may it be Ultrasound, CT scan or MRI and needs continuous evolution. Continuous evolving and developing medical imaging technologies need state- of -the art quality assurances and regulations as they are used on patients in every possible diagnosis. FDA’s Center for devices and radiological health (CDRH) is the regulatory body in US that is required to clear medical imaging therapeutic and diagnostic radiological devices intended to enter the market for sale.

Keywords: juniper publishers; medical imaging journals impact factor; journal of medical imaging impact factor; clinical and medical imaging; clinical lab and medical imaging reports; medical imaging and clinical research; current trends in clinical & medical imaging impact factor; international journal of clinical & medical imaging impact factor (search for similar items in EconPapers)
Date: 2016
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Persistent link: https://EconPapers.repec.org/RePEc:adp:jctcmi:v:1:y:2016:i:1:p:1-2

DOI: 10.19080/CTCMI.2016.01.555551

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