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Mexico Medical Device Market Access and ISO 13485 certification

Medical device manufacturers both in Mexico and around the world can leverage some of their expertise with their quality systems and products to open markets around the world.

The webinar explore the following points:
• How Mexican manufacturers can leverage their ISO 13485 / COFEPRIS MGMP certificates to access other markets.
• If you have ISO 13485 and want to go to Mexico, what do you do?
• Mexico medical device regulation and registration process for manufacturers in North America and the rest of the world,
• How that process interacts with ISO 13485 and the Mexican GMP, and
• If you're a device manufacturer in Mexico, the steps for CE marking.

We serve your passion for progress in the Medical Device (MD) and In Vitro Diagnostics (IVD) industry from the United States

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   1-301-495-0477

clientsWe're Hiring!

Due to our rapid growth in North America, we're seeking Lead Auditors, Certification Project Manager Active and Certification Project Manager - In Vitro Diagnostics responsible for medical device manufacturing clients.