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Emily Piernick

How to Develop an Agile Post-Market Surveillance Framework
By Emily Piernick on March 25, 2022

The resources required for compliance with the European Union Medical Device Regulation (EU MDR) and the In Vitro Diagnostic Regulation (EU IVDR)...

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4 Ways MSLs Can Make a Superhuman Impact through Scientific Exchange
By Emily Piernick on October 1, 2021

Medical Affairs teams have been challenged with an extreme reduction in face-to-face meetings. 

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