Ep 970 | How the FDA Removed ALL of the Safety Protocols in Developing the Shots | Guest: Dr. Jane Ruby

Ep 970 | How the FDA Removed ALL of the Safet...

Up next

The Hidden War on Red-State Land: Solar, Data Centers & the Death of Farming | 3/17/26

At a time of record losses in farming, red-state governments are destroying farmland with solar, wind, carbon capture, data centers, Section 8 overdevelopment, and everything other than what land should be used for. I also discuss how the dumb housing bill and HUD’s obsession wit ...  Show more

Stop Letting Islam Use America’s Constitution as a Human Shield for Jihad | 3/16/26

America’s founders never intended the Constitution to become a suicide pact that protects those who openly support our enemies. In this explosive episode, I break down why America’s immigration policies, political leadership, and legal system are failing to confront the growing t ...  Show more

Recommended Episodes

How Did One Woman Change the FDA's Drug Approval Process?
BrainStuff

When FDA employee Frances Kelsey called for caution regarding the drug thalidomide in the 1960s, she wound up saving babies and changing FDA guidelines as we know them. Learn more in this episode of BrainStuff, based on this article: https://history.howstuffworks.com/historical-f ...  Show more

Why doesn't the FDA regulate herbal supplements?
Stuff You Should Know

For thousands of years, societies across the globe have used herbs as medicine. While this practice continues today, the FDA does not regulate these potent substances. Find out why the FDA can't regulate herbal supplements in this HowStuffWorks podcast.

Learn more ...  Show more

#341: What NOT to say to FDA
Global Medical Device Podcast powered by Greenlight Guru

Description:Dive into the enlightening world of FDA inspections with Etienne Nichols and Mike Drues. In this comprehensive episode, the duo decodes the essence of effective communication, the importance of managing expectations, and the art of proactive dialogue with the FDA. The ...  Show more

#342: Planning an FDA Submission
Global Medical Device Podcast powered by Greenlight Guru

Description:In this episode, Ellie Reynolds, Associate Director of Quality Assurance and Regulatory Affairs at Proxima Clinical Research, dives deep into the complexities of FDA submissions for medical devices. She sheds light on the nuances of different submission types, such as ...  Show more