The FDA issued an emergency use authorization (EUA) that has the potential to decontaminate approximately 4 million N95 or N95-equivalent respirators per day in the U.S. for reuse by health care workers in hospital settings. Guidance Documents, Biologics Visit the Brightspace main homepage forlinks to Help videos to help you confidently navigate and use the features of Brightspace. FDA also added sodium citrate tubes used in blood specimen collection to the device shortage list. For the purposes of simple video conferencing, mobile devices such as smart phones or tablets do work, but your ability to collaborate with others will be limited. Webinar: Enforcement Policy for Personal Protective Equipment (PPE) During COVID-19: Immediately in Effect Guidance. , Education Events Lead at Arkansas Publishing Group, , Marketing Specialist at Springer-Miller Systems. The U.S. Food and Drug Administrations Center for Biologics Evaluation and Research (CBER) will convene a virtual meeting of the Vaccines and Related Biological Products Advisory Committee (VRBPAC) on June 10, 2021, via webcast. But then they recently added a Microsoft Teams integration (they formerly only had Zoom), and so now my practical need is resolved. Read written testimony. The FDA has scheduled a meeting of its Vaccines and Related Biological Products Advisory Committee (VRBPAC) on Feb. 26, 2021, to discuss the request for emergency use authorization (EUA) for a COVID-19 vaccine from Janssen Biotech Inc. FDA In Brief: FDA Updates Emergency Use Authorization for COVID-19 Convalescent Plasma to Reflect New Data. [CDATA[/* >