Mexico
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
Against any projection, 2020 has represented a challenge for any type of industry. The medical device was not the exception. Even though several statistics has
All Medical devices companies which import or export their products between different countries often deal with several legal documents required by the authorities. Such legal
Is this a real opportunity for those Medical Device manufacturers to participate without a sanitary registration? As published by the UNOPS (United Nations Office
