Description: The size of the Indian healthcare market today attracts many firms dealing in medical devices. This session will help small and medium-sized medical device firms, that harbour such ambitions, to better understand Indian regulatory requirements as per Medical Device Rules (2017) under the Drugs and Cosmetics Act (1940). It will help them design a viable regulatory strategy for marketing either through import or local manufacturing in order to provide products at competitive prices. This can also help firms cater other South Asian countries and markets in the Middle East. The session will also cover practical considerations from a regulatory point of view: protection of intellectual property and safeguarding company interest while marketing fully-compliant medical devices.
Learning Objectives:
Upon completion, participants will be able to acquire in-depth regulatory requirements of medical devices in India via the Medical Device Rules (2017) and other associated regulations.
Upon completion,participants will get exposed to various regulatory strategies for market entry to India, either import or local manufacturing through its own subsidiary or through an Indian company .
Upon completion, participant will get practical exposure from a regulatory point of view: protection of intellectual property and safeguarding company interest while marketing fully-compliant medical devices.