Verification based on Current Regulations.

Presentation of Dossier in time and manner before COFEPRIS, resulting in savings of time and money.

Check for Cohesion with the Information Presented.

Avoid or correct errors in the Integration of the Dossier, which will allow the product to launch into the market faster, by being authorized by COFEPRIS.

 Time Saving in the COFEPRIS review, as they review the Favorable Technical Report that we issued, which allows the authorization process to be more agile.

Security and Confidentiality of your Information in sending and receiving .

Extensive Experience in the Medical Devices and Medical Products Industry.