RE: All of the data is electronic and would be very easy to put together if it isn’t right now.
Can’t someone issue a FOIA request for these data?
The ACLJ and Judicial Watch should get in the act, they’re quite good and experienced at FOIA’s.
Isn’t an FOIA request by PHMPT precisely what brought this FDA response?
Also another question that comes to mind in reading this, has to do with the redaction of certain information. What does the FDA need to “redact” that would require staff to release an average of only 25 pages per day?
In the interest of full transparency, curious minds (and honest judges) should want to know.