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Does the pharma industry need to redefine the criteria for who can sponsor and execute clinical trials?

PDC Pharma Strategy CEO, Penelope Przekop, comments on this at the  FDA / Duke University-Margolis Institute for Health Policy public workshop, "Building Quality into the Design and Conduct of Clinical Studies: Integrating Quality by Design (QbD) and Risk-Based Monitoring (RBM) Approaches" on January 31st, 2024.  

learn more about pdc pharma strategy here

A conversation with Harsh Thakkar on Life Sciences 360: Building a Five-Star Career

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Talking about the science behind being the master of your destiny on GrasshoppHer

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A Conversation about 5-Star Career on The Chris Voss Show

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