FDA Guidance Regarding Emergency Use Authorizations and the Use of Investigational Products During the Pandemic Harvey M. Arbit, PharmD, MBA, President and CEO of Arbit Consulting, a firm that provides drug and medical device regulatory strategy and support for industry, academia, and investigator-initiated clinical research. He is adjunct professor at the University of Minnesota, College of Pharmacy, and adjunct professor at Albany College of Pharmacy and Health Sciences AND W
renda M. Teeple, PharmD, Chief Clinical Officer and Director of Regulatory affairs, Arbit Consulting; Clinical Pharmacist, Regions Hospital. She is Adjunct Professor, St. Catherine's University, Henrietta Schmoll School of Health, and Adjunct Assistant Professor, Albany College of Pharmacy and Health Sciences.
Engaging Non-English Speaking Participants and Families Remotely Idolly F. Oliva, MBA, Director Language Services, M Health Fairview
Assessing Capacity to Consent and Obtaining Informed Consent Remotely Abbey Staugaitis, RN, MSN, CCRC, Program Manager, ACRC, U of MN SIREN HUB Manager, StrokeNet RCC 18 Program Manager, Dept of Emergency Medicine, U of MN
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