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IRI-CE supports you in the regulatory strategy of your company in line with the commercial strategy in the different countries, in particular by providing services of:
- Regulatory positioning of medical devices
- Classification of medical devices
- Strategy according to the type of economic operator
- Regulatory strategy for export registrations (UK, Switzerland, US, Canada, Australia, Brazil, Japan, India...)
- Certification strategy (ISO, MDSAP CE marking, etc ...)

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