Qualtech Webinar: ENTERING INDIA'S MEDTECH MARKET — MEDTECH INDUSTRY OVERVIEW AND REGULATORY ROADMAP IN INDIA
- 2024-10-08 05:56:39
Join Qualtech's Webinar on India's Medical Device Market and Regulations
了解更多Join Qualtech's Webinar on India's Medical Device Market and Regulations
了解更多A new expert committee has been formed by the Government, to frame new laws for medicines, cosmetics and medical devices in a bid to replace the existing Drugs and Cosmetics Act which was formed in 1940.
了解更多More medical devices are being classified under India’s Medical Device Rule 2017 based on the intended use, risk associated with the device and other parameters. They include device categories ranging from nephrology and renal care, operation theatre, pain management, personal protective equipment (PPE), software, and general hospital medical devices.
了解更多More medical devices are being classified under India’s Medical Device Rule 2017 based on the intended use, risk associated with the device, and other parameters. They include device categories ranging from interventional radiology, rehabilitation, dermatological and plastic surgery, physical support, anesthesiology, and in-vitro diagnostic (IVD) medical devices.
了解更多As previously notified, the CDSCO has expanded the list of regulated medical devices in India, ranging from CT scan equipment, MRI equipment, defibrillators and more, in addition to all types of implantable devices
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