Medical Device Regulations in Mexico 2026

Mexico’s regulatory landscape for medical devices is shifting fast. With major updates to equivalency pathways, immediate approval modifications, GMP standards, and COFEPRIS leadership changes, global manufacturers need clarity now more than ever.

Join us for an expert-led webinar featuring Pedro Sánchez Neri, Consulting Manager at Emergo by UL, who has helped secure more than 100 Mexican registrations and has over a decade of hands-on regulatory experience.

Pedro will break down:

• How the new Equivalency Route for Regulatory Reference Authorities is reshaping submissions
• What’s changing in Immediate Approval Modifications and how timelines look
• What manufacturers must prepare for in 2026

If Mexico is on your regulatory roadmap, this is a session you can’t afford to miss.

Unable to attend the webinar live? Register anyway and we will send you the webinar recording.