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Executive Order 13996, officially titled Establishing the COVID-19 Pandemic Testing Board and Ensuring a Sustainable Public Health Workforce for COVID-19 and Other Biological Threats, was signed on January 21, 2021, and was the twelfth executive order signed by U.S. President Joe Biden.
In December, the FDA authorized the use of a rapid testing kit developed by Brisbane, Australia-based Ellume Health. The test is available for purchase without a prescription for about $30 and can give results in about 20 minutes. [62] [63] The FDA approved the test for people with and without COVID symptoms. [63]
The 2020 Coronavirus Aid, Relief, and Economic Security Act (CARES Act) enhanced FDA's ability to identify, prevent, and mitigate possible shortages of medical devices by requiring manufacturers to inform FDA of an interruption or permanent discontinuation of manufacturing during a public health emergency.
The test, which on Wednesday received emergency-use authorization from the U.S. Food and Drug Administration, measures the number of neutralizing antibodies that the body's immune system has ...
The first COVID-19 diagnostic test to be authorized for pooled samples, it can allow for testing on up to four individual swab specimens at a time, the FDA said. ... The U.S. Federal Drug ...
As the coronavirus pandemic engulfed the United States, Joe Shia, a consultant to Chinese medical companies, said he was bombarded with inquiries from American firms who saw a golden opportunity ...
Nationally Recognized Testing Laboratory is the term used by the United States Occupational Safety and Health Administration to identify third-party organizations that have the necessary qualifications to perform safety testing and certification of products covered within OSHA and each organization's scopes.
Only through compulsory vaccination will America accomplish the monumental task in front of us – getting to herd immunity. With Pfizer's FDA approval, employers should now require COVID-19 ...