2015, November

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.


Sarah STEC Legal and Regulatory Director, G-MED North America

Miguel Angel TORRES TELLO EmergoGroup Mexico

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