21st Century Cures Act - age of informed consent is over
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https://brownstone.org/articles/the-era-of-informed-consent-is-over/
…an exception from the requirement to obtain informed consent when a clinical investigation poses no more than a minimal risk to the human subject…The Act was designed to
…accelerate the discovery, development, and delivery of 21st-century cures, and for other purposes [?]…[emphasis added]
Some of the provisions within this Act make for uncomfortable reading. For example, the Act supported:
High-risk, high-reward research [Sec. 2036].
Novel clinical trial designs [Sec. 3021]
Encouraging vaccine innovation [Sec. 3093].
Wow... one could be subjected to a novel therapeutic drug trial and not be informed.... ??? Good read, though it is unsavoury, best to be informed.
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Very disturbing.
Children's Health Defense published an article about this back in Jan. Worth reading.
Lately I’ve been wondering if we can trust any pharmaceutical drugs? How do we know what is written on the label is actually what’s inside the packet?
Katherine Watt has been researching and writing about the legal framework put in place to facilitate the use of vaccines as bioweapons against people all over the world. This is her latest article.
Vaccine and related biological product manufacturing as US government-licensed poison manufacturing.
From the article
"The toxicity of vaccines and vaccine-related biological products has been incrementally increased over time.
Injuries and deaths caused by vaccines are falsely attributed to communicable disease, inherited genetic disorders and environmental exposures by the same public health, military and pharmaceutical manufacturing executives jointly running the intentional poisoning programs."
She has documented all her finding on her substack
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@Peatly
Thanks. Just perused her stack, looks good. Yes, as the FDA allows for secret or hidden ingredients, or "no msg added" BS, ergo anything may reside in your food, not only what is stated on the packet. What special ingredients were in the vaccines - new quadravalent jabs - that were first used in Northern Italy at the end of 2019, just before the plandemic antics?*From Doctorsinitaly . com website that I just found:
In September 2019 was made available for the first time in Italy a “cell-based” flu shot, called VIQCC or QIVc, that is produced from cultured animal cells rather than eggs.VIQCC is a quadrivalent flu vaccine that contains 2 type A viruses (H1N1 and H3N2) and 2 type B viruses. It is approved for people ages 9 and older.*
I remember that this was a big deal being discussed at the RPF in 2020, besides the intense air pollution in N. Italy, AND the high percentage of older Nortern Italians on various meds for Heart conditions. Hmmm.
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@AkJono UK introduced the same cell based flu shots in 2019. Great timing - I know people who came down with "the worst flu ever" and later called it covid.
Now we have a new method for estimating excess death which is equivalent to sweeping the deaths under the carpet
There are a lot of important vaccine info on the RPF being buried too - I imagine
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Thank you to prof. Fenton for exposing the skulduggery tactics used by the MHRA to bury data.
MHRA still won't release critical data on vaccinated pregnant women
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@Peatly
Even more evidence for me to shun all vaccines now.The book "dissolving illusions" had convinced me but now its undeniable
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A precedent setting case is being brought against Dr. Hoffe. If he loses this case, not only will his medical career be over, it will bring informed consent to an end, at least in Canada. He speaks to the UK Column
The Ethical Doctor—David v. Goliath: Dr Charles Hoffe
Moving interview - worth the time
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MP EU Christian Terhes Says Big Pharma Started Testing Covid Vaccine Since 2016
Entries in the VigiAccess database for covid 19 vaccines adverse reactions in humans went back to 2015 before the information was deleted.
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It is impossible to stay informed anymore regardless. The information flow is overwhelming. Even professional politicians do not have the time to read the bills they vote over. The only viable soloution is to limit the goverment.
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https://ted.europa.eu/en/notice/-/detail/506291-2020
From the document
IV.1.1.
Type of procedure
Award of a contract without prior publication of a call for competition in the Official Journal of the European Union in the cases listed belowThe procurement falls outside the scope of application of the directiveExplanation:
For reasons of extreme urgency under Regulation 32(2)(c) related to the release of a Covid-19 vaccine MHRA have accelerated the sourcing and implementation of a vaccine specific AI tool.
Strictly necessary — it is not possible to retrofit the MHRA’s legacy systems to handle the volume of ADRs that will be generated by a Covid-19 vaccine. Therefore, if the MHRA does not implement the AI tool, it will be unable to process these ADRs effectively. This will hinder its ability to rapidly identify any potential safety issues with the Covid-19 vaccine and represents a direct threat to patient life and public health.
Reasons of extreme urgency — the MHRA recognises that its planned procurement process for the SafetyConnect programme, including the AI tool, would not have concluded by vaccine launch. Leading to a inability to effectively monitor adverse reactions to a Covid-19 vaccine.
Events unforeseeable — the Covid-19 crisis is novel and developments in the search of a Covid-19 vaccine have not followed any predictable pattern so far.
IV.1.3.
Information about a framework agreement or a dynamic purchasing system
IV.1.8.
Information about the Government Procurement Agreement (GPA)
The procurement is covered by the Government Procurement Agreement: yes
IV.2.
Administrative information........................................
US Government Paid News Media $1 Billion to Promote Vaccines
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Edit to add this articleJacob Rees-Mogg claims UK government 'downplayed' risks of AstraZeneca COVID vaccine
