Description

The medical devices and diagnostics industry is going through one of the most challenging times in its history. While the industry has to put significant measures in place to respond to Covid-19, from submitting urgent filings, to dealing with supply chain interruptions and adapting to a new way of collaborating, regulatory teams are still having to keep up and plan for changes like European MDR and IVDR, which puts an enormous focus on transparency to improve patient safety. 

Join this webinar by Veeva Systems to learn how Alcon, Roche Diagnostics, Baxter and GE Healthcare have addressed these challenges with different approaches to transform their regulatory operations and create agile, sustainable models that reduce administrative burden and enable regulatory affairs professionals to focus on key activities. 

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