The FOIA request was submitted to the FDA in August by Public Health and Medical Professionals for Transparency, a group of more than 30 international public health professionals, medical professionals, scientists, and journalists that "exist solely to obtain and disseminate the data relied upon by the FDA to license COVID-19 vaccines." The group includes academics and medical experts from Yale, Harvard Medical School, and UCLA; alumni from the Trump administration; and prominent health experts from around the world.
PHMPT is being represented by Siri & Glimstad, a New York-based law firm that has performed millions of dollars of legal work on behalf of groups opposed to vaccine mandates.
The medical transparency group had requested "all data and information for the Pfizer vaccine" including safety and effectiveness data; a protocol for a test or study; adverse reaction reports, product experience reports, consumer complaints, and other similar data and information; a list of all active ingredients and any inactive ingredients; an assay method or other analytical method; all correspondence and written summaries of oral discussions relating to the vaccine; all records showing Pfizer and BioNTech's testing of a particular lot; and all records showing the testing of and action on a particular lot by the FDA.
PHMPT also made a request for expedited processing of its FOIA submission, arguing there is a "compelling need" for the FDA to speedily release Pfizer vaccine data "because a lack of transparency erodes the confidence the medical and scientific community and the public have in the conclusions reached by the FDA."
FDA asks federal judge for 55 years to complete FOIA request for Pfizer vaccine information
PHMPT is being represented by Siri & Glimstad, a New York-based law firm that has performed millions of dollars of legal work on behalf of groups opposed to vaccine mandates.
The medical transparency group had requested "all data and information for the Pfizer vaccine" including safety and effectiveness data; a protocol for a test or study; adverse reaction reports, product experience reports, consumer complaints, and other similar data and information; a list of all active ingredients and any inactive ingredients; an assay method or other analytical method; all correspondence and written summaries of oral discussions relating to the vaccine; all records showing Pfizer and BioNTech's testing of a particular lot; and all records showing the testing of and action on a particular lot by the FDA.
PHMPT also made a request for expedited processing of its FOIA submission, arguing there is a "compelling need" for the FDA to speedily release Pfizer vaccine data "because a lack of transparency erodes the confidence the medical and scientific community and the public have in the conclusions reached by the FDA."
FDA asks federal judge for 55 years to complete FOIA request for Pfizer vaccine information
