The mexican registration Holder (MRH) pays. The receipt must be included in the final dossier.

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If distributors will not be added to the registration at this time, they must be added later through a modification process.

All Mexican distributors are legally required to have these noties. An electronic copy of the notices is sufficient for the registration.

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Issuing authority to the legal representative in order to apply for renewals and/or registration submissions to COFEPRIS. An original or certified copy is required.

Simple copy of the document.

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Labels must be in Spanish and should meet the requirements of the Mexican Labeling Norm NOM-137-SSA1-2008. Whenever Mexican Labels are not yet finalized and compliant, it is necessary to prepare and submit the Label Design.

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At least the following information must be provided: Name, Description of the product, intended use and directions of use, list of product components or parts, assembly and disassembly instructions, operating and clean up instructions, operation conditions and storing, warnings, cautions, contraindications and adverse events, other as applicable (maintenance, calibration, preparation), for contrast media, indicate route of administration, pharmaceutical form and content of active ingredient per dose unit.

Report summarizing latest post marketing surveillance of the product. It includes all adverse events recorded since the product was first made available on the market (if applicable). It also includes the corrective and preventive actions taken.

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Issued in the design/development of the medical device, demostrating foreseen adverse incidents which should be included in the labels, IFU and/or Operating Manual. This doesn't need to be submitted to COFEPRIS, but it needs to be kept on file by the Mexican Registration Holder.

You will receive the template for the letter from the consultant during the dossier compilation process. Original or Certified Copies are required.

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You will receive the template for the letter from the consultant during the dossier compilation process. Original or Certified Copies are required.

Coded certificate issued within the last year, including the device to be registered before COFEPRIS. Original or Certified copy

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It must include: description, intended of use, codes or presentations, formula and/or compositions when applicable, shelf life when applicable, sterility period, primary and secondary packaging description.

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It must include: description, intended of use, codes or presentations, formula and/or compositions, shelf life, when applicable, sterility period, primary and secondary packaging description.

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It must include: description, intended of use, codes or presentations, formula and/or compositions, shelf life, when applicable, sterility period, primary and secondary packaging description.

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