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We have quality processes that allow us to maintain confidentiality and carry out the correct integration of the Dossier for the required process.


At I3CGLOBAL we carry out an effective process by current regulations, reducing the risk of prevention by the authority.


We are a Company that provides Consulting and Management services to support the regulatory and commercial area of ​​our clients to obtain Authorizations, Notices, Permits, Licenses and Sanitary Records and various procedures before COFEPRIS& CNSNS


For us, it is a pleasure to serve you, supporting our CLIENTS in achieving their objectives, through our work team with more than 10 years of experience offering our services for the Pharmaceutical, DM, Distribution and Marketing sector leaders at national and international level. complying with the client’s requirements: quality and service. Medical Device CE Marking


Provide consulting and quality service to our clients in regulatory matters of health supplies and products, facilitating their manufacture, use, maintenance, import, distribution, marketing and regulatory compliance.


To be the leading consultancy in regulatory matters of health supplies and products, which facilitates our clients with regulatory compliance and health protection.


At I3CGLOBAL we are committed to the satisfaction of our clients by offering services in regulatory matters and translations, by current health regulations, under a quality system and continuous improvement. Medical Device Consultants


Our services are performed under the controls established by a quality management system that meets the ISO9001: 2015 requirements.



Published at: Recent Health Articleshttp://recenthealtharticles.org

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