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

Revolutionising the Medical Device Industry What is Health 4.0? Health 4.0 is a concept that arises from the fourth industrial revolution, or

The Good Manufacturing Practices (GMP) Certificate is the legal document that certifies that the company manufactures its products under conditions and practices

In Mexico, Medical Devices are classified according to the risk involved in their use, for registration purposes, so we have the following