Food Drug Administration FDA released final guidance documents to assist with the transition of medical devices that were legally distributed: subject to certain enforcement policies issued during the COVID-19 public health emergency PHE, Emergency Use Authorizations EUAs.
On March 27, 2023, the U.S. Food & Drug Administration (FDA) released two final guidance documents to assist with transitioning medical devices: (i) that were subject to certain enforcement policies.
On January 31, 2020, in response to the COVID-19 pandemic, the Secretary of Health and Human Services (HHS) issued a declaration of a public health emergency (PHE) under Section.
This week, the U.S. Food & Drug Administration (FDA) issued two much anticipated guidances, each outlining how COVID-19 devices will be treated after the expiration of the COVID-19 public health emergency (PHE).