Our specialized team provides comprehensive advice on regulatory activities related to the manufacture and distribution of medical devices. Our highly trained and experienced professionals are here to guide you through the complex regulatory processes, ensuring that your company complies with all applicable regulations and requirements.

What can we do for you?

Technical Responsible service for manufacturing and importing medical devices. 
Operating procedures preparation and implementation support for activities and products included in the operating license.
Preparation of the AEMPs operating license report for manufacturers, groupers, importers and sterilizers of medical products.
Processing and monitoring of the application with the AEMPs.
Preliminary audit and advice on adaptation of manufacturing and import facilities.
Communication service for marketing of medical devices.
Advice on regulatory activities related to the manufacture, import and distribution of medical devices. 

Our team of professionals is ready to listen and assist you

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