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