Broad-scale informed consent: A survey of the CTSA landscape by Redonna Chandler, Kathleen T. Brady, Rebecca N. Jerome, Milton Eder, Erin Rothwell, Kimberly A. Brownley, Paul A. Harris

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Software to manage regulatory workflows for medical device development at academic medical centers: A critical gap by Lynn Rose, Jennifer McCaney, Gaurav Dave, Kimberly A. Brownley, David Sheridan, Payal Shah, Grzegorz Zapotoczny, Juan Espinoza

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Informed consent: Old and new challenges in the context of the COVID-19 pandemic by Erin Rothwell, Donna Brassil, Marietta Barton-Baxter, Kimberly A. Brownley, Neal W. Dickert, Daniel E. Ford, Stephanie A. Kraft, Jennifer B. McCormick, Benjamin S. Wilfond

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ReGARDD (Regulatory Guidance for Academic Research of Drugs and Devices): The evolution of a collaborative regional CTSA-funded forum and website for regulatory support by Kimberly A. Brownley, Marie Rape, Amanda Wood, Gaurav Dave, Chad Henderson, Diana Severynse-Stevens, Mike Zmuda, Diane Earp, Carmella Moody, Issis Kelly-Pumarol, Joseph Andrews, Kristen M. Foss, Stephanie Fraser, Erika Segear, Amanda B. Parrish

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