Colombia reduces requirements for products from reference countries
This article was originally published in SRA
Medical device registration requirements in Colombia have been reduced for companies seeking to register low- and medium-risk devices that are already approved in certain reference countries or areas1.
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Colombia's health ministry says it is aiming to complete by year-end the implementation of regulations that allow manufacturers and importers to parallel import certain medical devices into the country without having to register them with the national healthcare products regulatory agency, INVIMA1.