CE Marking support for In Vitro Medical Diagnostic Devices (IVD)

The realization, aimed at placing on the market, of In Vitro Diagnostic Medical Devices (IVD) requires a thorough and rigorous analysis and preparation of the reference technical documentation in accordance with the relevant regulatory requirements.

Biofield Innovation is able to offer support in the collection and processing of the information necessary for the realization of technical product documentation in order to obtain and maintain the CE marking according to current legislation.