*{All 3 are idea posts about removing legal immunity from pharma/vaccine manufacturers. The post that is called remove immunity from pharma has the most votes so it should be the parent post. The post about the 1986 act specifies what previous pegal action should be repealed. } *
All vaccine trials must have an IRB to make sure the negatives do not out way the positives. If the IRB determines that the vaccine and/or MRNA study is too risky, then the trial is prevented from moving forward.
I work for a company that provides drug trial software for big pharma. The FDA needs to look at how fast someone is filling out form data, which is being collected. You can tell if someone is cheating by the amount of time they spent filling out the form. There’s much more that can be done to make sure data is clean and valid. The FDA needs to do more to detect bogus data.
All clinical trials must be minimum of 1 year in length in duration and the control panel cannot be another vaccine , can only use a placebo as control panel medication or vaccine. All subjects in clinical trial must be reported on.