Dear Chairman Massie,

Thank you for the invitation to testify before the House Judiciary Subcommittee … in the hearing titled, Follow the Science?: Oversight of the Biden Covid-19 Administrative State Response.

Our firm’s vaccine practice, which spans vaccine injury, exemptions, and policy, has over forty professionals. In our lawsuits, we must prove claims regarding these products with government and high impact journal data and sources. Appeals to credentials do not suffice.

Please find below a few points regarding Covid-19 vaccines we believe provide a broader framework in which to consider the administrative state’s actions regarding these products. While these points may conflict with the cultural cognition of some, based on our experience, they reflect the best available evidence.

EIGHT sections — 18 page total (pdf)

1. Covid-19 Vaccine Trials Were Robust When Compared with Other Vaccine Trials

2.Covid-19 Vaccine Trials Anemic When Compared to Drug Trials

3.Economic Interest to Assure Safety in Drug Trials Absent in Vaccine Trials

4.HHS’s Promotion and Defense of Vaccines Conflicts with Regulatory Duties to Identify and Disclose Safety and Efficacy Issues

5.Examples of Structural Conflicts Impacting Covid-19 Vaccine Trials

6.Preventing Transmission, an Example of Dogma Driving Policy

7.FDA and CDC Hide Concerning Post-Licensure Safety Data from Public

8. FDA Failed to Enforce its Own EUA Conditions Concerning Promotional Material for Covid-19 Vaccines

https://judiciary.house.gov/sites/evo-subsites/republicans-judiciary.house.gov/files/evo-media-document/Siri%20Testimony.pdf

Also available at (not as easy to read) –> https://x.com/AaronSiriSG/status/1807862081322209632