Mexico
As mentioned in our Classification and Grouping Ultimate Guide, there are a series of rules to classify and group medical devices. The above-mentioned rules are
One of the requirements to register a medical device in Mexico is to have a warehouse to store the product. Although there are no rules regarding the exact size
Last March 19th 2021, COFEPRIS published a guideline with rules and requirements related to COVID-19 (SARS-CoV2 virus) supplies in Mexico. Even though the purpose of
MDSAP and its implementation for Sanitary Registration of Medical Devices in Mexico with Equivalency Agreements Since 2012 the International Medical Device Regulators Forum (IMDRF) has been working in
Technovigilance, or Medical Device Surveillance, is the activity that ensures that any medical technology in Mexico is correctly working and describes how to report any incident related to the
Introduction Last November the 18th 2020, the Ministry of Health in Mexico released a note through the Official Diary establishing new expedited timelines for
