About apostilled documents in the medical device industry
All Medical devices companies which import or export their products between different countries often deal with several legal documents required by the authorities. Such legal
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All Medical devices companies which import or export their products between different countries often deal with several legal documents required by the authorities. Such legal
Is this a real opportunity for those Medical Device manufacturers to participate without a sanitary registration? As published by the UNOPS (United Nations Office
In the last months, COFEPRIS has been implementing different activities to digitalize new procedures focusing on a paperless policy. In this article, we briefly describe
As we have previously explained in our Guide and Article, COFEPRIS is the regulatory arm of the Ministry of Health in Mexico which regulates the
In recent months, due to the global pandemic, there have been several changes in medical devices market and its regulation in Mexico. In this article,
As mentioned in our Classification and Grouping Ultimate Guide, there are a series of rules to consider when classifying and grouping medical devices. The above-mentioned