"In response to a question about the nature of US
Post# of 9122
The process is called a pre-EUA submission, and USAMRIID experts provided data to FDA so that if a dangerous outbreak occurred, the FDA could quickly transition the diagnostics into use under an emergency declaration.
Determining likelihood of emergency outbreaks
At the time, Norwood said, USAMRIID submitted 73 assays to the FDA and engaged several subject-matter experts to try to determine which of the assays would be critical for emergency outbreaks.
“Time and time again,” Norwood said, “the filoviruses came up as the No. 1 priority, so we were … concerned about this.”
It all depends on DTRA's priorities....but the US Army has been looking at diagnostics for years.