IVDs for Management of COVID-19 Patients.Antigen Diagnostic Tests for SARS-CoV-2.Molecular Diagnostic Tests for SARS-CoV-2.COVID-19 Tests Granted Traditional Marketing Authorization by the FDA.In Vitro Diagnostic EUAs: Overview and Templates Webinar on Guidances on COVID-19 Transition Plans for Medical Devices - April 18, 2023.
Transition Plan for Medical Devices Issued Emergency Use Authorizations (EUAs) Related to Coronavirus Disease 2019 (COVID-19).Transition Plan for Medical Devices That Fall Within Enforcement Policies Issued During the Coronavirus Disease 2019 (COVID-19) Public Health Emergency.In particular, for manufacturers planning to seek marketing authorization for their devices, the FDA recommends beginning work on a marketing submission, including a transition implementation plan, as described in the guidances. The FDA encourages stakeholders to review the two final guidances, view the webinar, and reach out to the FDA if they have questions or concerns. Taking other actions with respect to these devices.Developing a transition implementation plan,.The guidances outline the FDA's general recommendations to transition from certain policies adopted and operations implemented during the COVID-19 pandemic to normal operations, including the FDA's recommendations for: MaThe FDA has finalized two guidances: Transition Plan for Medical Devices That Fall Within Enforcement Policies Issued During the Coronavirus Disease 2019 (COVID-19) Public Health Emergency and Transition Plan for Medical Devices Issued Emergency Use Authorizations (EUAs) Related to Coronavirus Disease 2019 (COVID-19).
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