Molecular Diagnostics Europe 2018 | The Changing Regulatory Requirements in the EU

from CHI Podcasts · host Cambridge Healthtech Podcasts

Dr. Andreas Stange of TÜV SÜD talks about the practical impact of the new IVD regulation, how it will affect manufacturers and notified bodies, challenges in validation, and practical advice to prepare for these changes in companion diagnostics. For more information, please visit http://www.MolecularDXEurope.com/MDXE_Content.aspx?id=190671

Episode metadata supplied by the publisher feed · Published Mar 19, 2018

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Molecular Diagnostics Europe 2018 | The Changing Regulatory Requirements in the EU

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