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Considerations to Improve Patient Outcomes in Early Drug Development, Upcoming Webinar Hosted by Xtalks
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In this free webinar, attendees will learn about developing a framework for handling multiple endpoints for the drug’s go-to-market label and determining the potential of adaptive design for optimizing the trial. The featured speakers will discuss key interactions and questions to ask when seeking regulatory input of pivotal study designs.
A comprehensive examination of the roles played by all participants has the potential to produce faster and more concrete results, leading to improved patient outcomes. TORONTO (PRWEB) March 17, 2021 Every drug development program must begin with a thorough identification of all relevant stakeholders patients, physicians, regulators, investors and an understanding of how they factor into the development process. It’s not just a matter of courtesy; a com