“…everybody look what’s going down.”

The author is the inventor of mRNA vaccine delivery, not the current Covid vaccines:

“…if I were to propose a clinical trial involving children and entice participation by giving out ice cream to those willing to participate, any institutional human subjects safety board (IRB) in the United States would reject that protocol.

If I were to propose a clinical research protocol wherein the population of a geographic region would lose personal liberties unless 70 percent of the population participated in my study, once again, that protocol would be rejected by any US IRB based on coercion of subject participation.

No coercion to participate in the study is allowed. In human subject clinical research, in most countries of the world this is considered a bright line that cannot be crossed. So, now we are told to waive that requirement without even so much as open public discussion being allowed?”

More at the link from Robert Malone, M.D.

trialsitenews.com

See more here: budbromley.blog

Please Donate Below To Support Our Ongoing Work To Expose The Lies About COVID19

PRINCIPIA SCIENTIFIC INTERNATIONAL, legally registered in the UK as a company incorporated for charitable purposes. Head Office: 27 Old Gloucester Street, London WC1N 3AX. 

Trackback from your site.

Comments (3)

  • Avatar

    Tom O

    |

    Actually, the article that was quoted from is so short, I don’t understand why the whole thing isn’t here. It is extremely important to understand the “bioethics” he is referring to, and even more so, the reason that he wrote the article. It’s a shame you didn’t bring the entire article over.

    Reply

    • Avatar

      Jerry Krause

      |

      Hi Tom O and PSI Readers,

      Tom O’Sullivan, long time editor of PSI, has taught me to be brief because his targeted READERS do not have time to read long articles.

      Tom O, what more can be said if one does not understand that which was written???

      Have a good day, Jerry

      Reply

  • Avatar

    Tom

    |

    The trial and study process for all drugs, vaccines and mRNA injections is extremely flawed. The true ARR, or absolute risk reduction calculations are usually well below 5%. Cancer drugs are approved using surrogate studies which use minimal data so that they can get on the market sooner and earn big profits for pharma years ahead of knowing if they are any better than previous drugs.

    Same with the latest Alzheimer drug. At over $50k a pop, pharma wants it on the market to get the big bucks before we even know if it is any good. It will also fail, as do 98% of new drugs.

    We can see first hand with the mRNA spike protein injections that have hardly been tested how demanding big pharma is to get everyone injected very quickly. Why? Where is the true Black Plague that we need protection from? CoV-2…not much more than an hyper flu that may be a bit more deadly than the seasonal flu. Besides, these injections have NOT been proven to be effective at all against covid-19.

    Pharma is complaining that the CDC is saying a booster shot is not necessary. By the way, those booster shots will not require any previous testing. Nor does any alterations in the spike proteins. What a great system we have for protecting the public’s health…shoot first, ask questions later, just as long as big pharma is raking in big profits. That’s the bottom line!

    Reply

Leave a comment

Save my name, email, and website in this browser for the next time I comment.
Share via