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FDA Issues Draft Guidance for Sponsors and Other Stakeholders on Using Registries as RWD to Support Regulatory Decision-Making | Faegre Drinker Biddle & Reath LLP

The U.S. Food and Drug Administration (FDA) issued its third draft guidance under the Real-World Evidence (RWE) Program on November 29, 2021. In Real-World Data: Assessing Registries to.

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Xtalks Announces Its Life Science Webinar Calendar for December 2021

Toronto, ON (PRWEB) December 01, 2021 Stay on top of current hot topics through free webinars presented by leading experts in the pharma, biotech, medical

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