Registration checklist for Software as a Medical Device in Mexico according to Article 83 of the ‘Health Supplies Regulation’
£35.00
Simplify the registration process for your Software as a Medical Device in Mexico with this detailed, regulation-compliant tabulated checklist
English
This chart provides a tabulated checklist of the registration requirements that apply to Software as a Medical Device in Mexico, according to Article 83 of the Health Supplies Regulation. For each entry of administrative or legal information, the table includes the legal basis for the registration requirement, the element that integrates the requirement, and supplementary information.
Specification: 13 pages plus covers, in English, supplied by email as a PDF.
This article has been published in the May 2024 issue of the Journal of Medical Device Regulation.
