Georgia Division Of Public Health
Our resource pages includes guidance for travelers, sources for healthcare suppliers, and informational materials in multiple languages. The New Jersey COVID-19 Information Hub offers New Jerseyans with the most up-to-date details about COVID-19 and the State’s response, including details about companies similar to meals help and small business help. Alaska Coronavirus Response Hub updates usually occur by noon and provisional information are topic to vary. The data hub will replace a Monday via Friday schedule, with no updates made on weekends or state holidays.
Dr. Patrizia Cavazzoni, the appearing director of FDA’s Center for Drug Evaluation and Research, joins Dr. Shah for an in-depth dialogue on clinical trials and treatments for COVID-19. FDA’s Coronavirus Treatment Acceleration Program leverages cross-agency scientific assets and experience to bear on COVID-19 therapeutic development and evaluation. The FDA’s consumer protection work is a cornerstone of our mission and a critical component of our pandemic response efforts. The FDA authorized the first two COVID-19 serology checks that display an estimated amount of antibodies present in the individual’s blood. Advanced manufacturing offers an strategy for protecting our supply chain and bettering our response capability throughout crisis conditions.
Resources For More Healthy Dwelling
FDA actions on warning letters concerning fraudulent products, approval of an abbreviated new drug application for a drug to facilitate tracheal intubation, and extra in its ongoing response to the COVID-19 pandemic. FDA actions on vaccine research, issuances of emergency use authorizations, and extra in its ongoing response to the COVID-19 pandemic. FDA actions on hand sanitizer recalls, testing-related emergency use authorizations, Industry Hotline closure, and extra in its ongoing response to the COVID-19 pandemic. FDA actions on consumer fraud; reissuance of an EUA for a diagnostic test; steering for transport media; extension of enforcement discretion for human cell, tissue, and mobile and tissue-based mostly products; and extra in its ongoing response to the COVID-19 pandemic. FDA actions on issuances of emergency use authorizations, exams, and extra in its ongoing response to the COVID-19 pandemic.
Learn extra about how FDA is facilitating the development and availability of medical countermeasures and defending the public well being. The FDA up to date a policy initially issued on Feb. 29 on diagnostic testing for coronavirus (COVID-19) to be able to achieve extra fast testing capability in the U.S. The FDA hosted a stakeholder call to discuss food safety and food provide questions, respond to concerns, and highlight key FDA resources for the response to the COVID-19 pandemic. The FDA issued the primary emergency use authorization for some extent-of-care COVID-19 diagnostic for the Cepheid Xpert Xpress SARS-CoV-2 check. The FDA issued an emergency use authorization for a blood purification system to deal with patients 18 years of age or older with confirmed Coronavirus Disease 2019 (COVID-19) admitted to the intensive care unit with confirmed or imminent respiratory failure.