In previous articles and guidelines, we have explained the registration process for medical devices in Mexico though the so called

Unlike other countries, in vitro diagnostics IVDs in Mexico are considered as medical devices and thus subject to general regulations

In recent months, COFEPRIS has been experiencing a series of changes with the aim of attending overdue requests. In this

Medical devices are a broad group of products with different characteristics. Thus, many standards have been developed to establish general

In general terms, combination products consist in a pharmaceutical product including chemical synthesis molecules, biologic or biotechnological API’s, that are

In general terms, tariff codes are a series of numbers to identify products for international trade purposes. These codes are