Mexico
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
Medical device labeling includes all labels, instructions for use (IFU), and any written, printed, graphical, or electronic information provided by the manufacturer that accompanies a device.
Introduction In recent months there have been new changes in laws and regulations that had led to an international tender for the consolidated purchase
