By Stewart Eisenhart, Emergo Group
India’s medical device registration system is still transitioning to a more formalized and predictable framework, which has raised questions from foreign manufacturers about what regulators do and do not currently require for market authorization in the country. In many cases, one requirement foreign firms can be sure of is the need to obtain an import license in order to properly register their products in India.
Get the full story here at the Emergo Group’s blog.
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