On July 7th, 2025, an agreement was published that brings important changes to medical devices in Mexico. This new document, which came

Breaking into Mexico’s healthcare market is no small feat. For international manufacturers, Mexico’s COFEPRIS— Federal Commission for the Protection against Sanitary Risk—regulations

On July 7th, 2025, an agreement was published that brings important changes to medical devices in Mexico. This new document, which came

Companies that distribute and market medicines for human use within national territory must have a warehouse to store the medicines they are

Cofepris, in an attempt to encourage the reporting of adverse reactions by consumers and healthcare professionals, launched a new platform for notifications.

The Medical Device Single Audit Program (MDSAP) represents a significant collaboration in the field of international health regulation, designed to improve the