MEDICAL DEVICE REGULATION

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Anjali Suresh Bansode; Ms.Bhagyashali  Baheti

MEDICAL DEVICE REGULATION

Authors: Anjali Suresh Bansode, Ms.Bhagyashali Baheti

Unique Paper ID: 177690
Volume: 11
Issue: 12
PageNo: 1222-1230

Keywords: No Keywords Found

Abstract:
This abstract provides a brief overview of medical device regulations in India, including, advantage of disposable medical device regulations and disadvantage of disposable medical device regulations. this abstract also provides security challenges of medical devices and also include History of medical devices regulations and its overview. Patient care for the practicing physician increasingly relies on medical devices. The U.S. Food and Drug Administration is responsible for the safety and effectiveness of medical devices in the United States. In addition to playing a role in the clinical use of devices, physicians may also participate in their design, production, use, and safety by expressing their need for certain products, by providing practical input and feedback into product design, by participating in device-related research, and by reporting device-related adverse events.

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ISSN: 2349-6002
Volume: 11
Issue: 12
PageNo: 1222-1230

MEDICAL DEVICE REGULATION

Available:https://ijirt.org/article?manuscript=177690

Impact Factor
8.01 (Year 2024)

UGC Approved
Journal no 47859

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