Abstract
India is a nation that constitutes approximately 17% of the
World’s population. People from around the world flock to India for#surgeries and advanced #treatment as the facilities are top-notch yet
affordable. Prior to 2005, India did not have a regulatory policy for
#MedicalDevices, while Drugs and #Cosmetics were brought under
the ambit of Regulation. In 2017, the Indian government issued
a set of guidelines for the Regulation of Medical Devices. This
guideline will be taking effect in 2018. This paper aims to explain
the regulatory process in India and offer a perspective on the same.
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Medical Device Regulation in India by Aishwarya Bhargav in BJSTR
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