BioPhorum introduces – EU MDR regulation

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Broadcast date

Thu, Dec 16, 2021

 

Presented by

    Tara Cox - Takeda

 

Quick Description

The drivers that instructed the update and the biggest changes that will impact the biopharmaceutical industry

Details

Tara Cox, Head of Device Quality and Regulatory Compliance at Takeda talks us through the updated EU MDR regulation, the drivers that instructed the update and the biggest changes that will impact the biopharmaceutical industry. How is BioPhorum helping to address the challenges that are anticipated in supporting the products?

Speakers

Tara Cox

Head of Device Quality and Regulatory Compliance

Takeda