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@article{177690,
        author = {Anjali Suresh Bansode and Ms.Bhagyashali  Baheti},
        title = {MEDICAL DEVICE REGULATION},
        journal = {International Journal of Innovative Research in Technology},
        year = {2025},
        volume = {11},
        number = {12},
        pages = {1222-1230},
        issn = {2349-6002},
        url = {https://ijirt.org/article?manuscript=177690},
        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.},
        keywords = {},
        month = {May},
        }