You can look up specific clinical trials at the website www.clinicaltrials.gov. There are also resources here for those wanting to participate.
There is a large body of federal law regulating how clinical trials are conducted:
Regulations: Good Clinical Practice and Clinical Trials.
Note that line #3 specifically addresses informed consent and line #5 addresses the ethics reviews (Independent Review Boards). These are 21 CFR Part 50 and 21 CFR Part 56, if you actually want to read the regulations.
The federal regulations do not just cover human subjects, they also specify ethical treatments of animals in pre-clinical research.
If you think that any pharmaceutical company can somehow get away with skirting federal law, keep in mind that their data must be shared with the FDA. The FDA upholds federal law. Imagine if you had to share all of your financial data on a regular basis with an IRS agent--not a tax form but an actual agent who has access to all of your bank records. That is pretty much the situation with pharmaceutical companies or research institutions and the FDA. Companies have to spend $1-2 billion dollars per drug to conduct all of the research and clinical trials necessary to satisfy the FDA.
I was involved in pre-clinical testing of drug candidates. Once, we gave a drug to rabbits and one of them died. Our FDA representative stopped further research on that drug immediately. We had to investigate why the rabbit died and show that it died because of a physiological difference in drug metabolism between rabbits and humans before the FDA allowed us to proceed with our research. This investigation took months, and probably cost tens of thousands of dollars.
Since the FDA immediately halts research on a drug after a rabbit dies, do you seriously think the FDA is going to allow pharmaceutical companies to market a drug that is harmful to humans?
“do you seriously think the FDA is going to allow pharmaceutical companies to market a drug that is harmful to humans? “
Why not the pharmaceutical companies are protected from consequences and large amounts of money are in the mix.
You are surprisingly naive if you believe the FDA functions as a functional regulatory body any more given their incestuous relationship with the pharmaceutical companies.
Scott Gottlieb anyone?
Over 96,700 people die from drug overdoses in a year.Opioids are a factor in 7 out of every 10 overdose deaths.
Drug overdoses have killed almost a million people since 1999.
Trials are before approval, except in this case the Scamdemic overseers claimed it was an emergency and that could release the bioweapon without testing. Pfizer even dismissed their test group.
Those who were coerced into it, especially with their livelihood at stake weren't willing participants.
It's an absolute farce to pretend the Jim Jones Jab is a vaccine and that it went through clinical trials.