In Vitro Diagnostics

In Vitro Diagnostics Medical Devices BSIThe In Vitro Diagnostics Directive (IVDD) 98/79/EC  is a set of regulatory requirements that medical device manufacturers must comply with in order to place a CE marking to their product for the European market.

As an IVD Notified Body, our team of specialists and technical experts can help you obtain IVDD compliance in order to get your devices to market.







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