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

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

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

The CHI Podcasts are produced by the Cambridge Healthtech Institute and offer in-depth interviews with research and business leaders from many facets of biotechnology.

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

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