Medical Devices Technologies In Vitro Diagnostics

What is the IVD Directive

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.

Why choose BSI for your product compliance to Directive (IVDD) 98/79/EC?

Stay up to date with the latest updates from BSI