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ISSN: 2574 -1241
ISSN: 2574 -1241
Received: April 19, 2018; Published: April 27, 2018
DOI: 10.26717/BJSTR.2018.04.001008
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 Medical Devices, 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.
International Association of Landscape Archaeology, Czech Glass Society, Czech Republic
Department of Chemistry, Semenov Institute of Chemical Physics, USSR Academy of Sciences, Moscow, Russia
Pharmaco-kinetics, dynamics and Drug Metabolism, Touro College of Pharmacy, USA
Professor of Nuclear Medicine, Faculty of Medicine and Surgery, University of Milan, Milan, Italy
Associate Professor at Department of Breast and Thyorid Surgey, Chongqing General Hospital, China
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