in vitro device

EU Commission Proposes to Extend MDR/IVDR Deadlines

The Commission of the European Union (EU) has proposed extending the transition period for...

The EU’s MDR and IVDR Are Published!

The European Union’s (EU’s) new regulations applicable to medical devices and in vitro diagnostic devices have finally been published.

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Introduction to Shielding

ARRL Files Comments in Response to U.S. FCC’s Deregulation Plans

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