Anonymous ID: 0251f9 Feb. 1, 2024, 11:22 a.m. No.20341691   🗄️.is 🔗kun

(you) are more Powerful than you Know

The[y] that wish to control you

-Need you to participate-

Without (you), nothing happens

Anonymous ID: 0251f9 Feb. 1, 2024, 11:25 a.m. No.20341698   🗄️.is 🔗kun

See Evil, Reject Evil

Don't give them your Money, Time or Energy

 

Once they are exposed as Evil

They will always be Evil

Anonymous ID: 0251f9 Feb. 1, 2024, 11:30 a.m. No.20341712   🗄️.is 🔗kun

Once Evil is Exposed

The[y] wil ltry & Say they are not

 

Do not ignore your Eyes and Ears

Cut Evil out of your Life, -Forever-

 

Even the Devil can Quote Scripture when it suits hs needs

Anonymous ID: 0251f9 Feb. 1, 2024, 11:38 a.m. No.20341735   🗄️.is 🔗kun   >>2025 >>2178 >>2299

FDA Quietly eliminates need for Informed Concent

 

“Obtaining informed consent from those who volunteer to participate in research is a fundamentally important principle of human subject protection. The quality and integrity of clinical research is something the agency takes very seriously and the protection of research individuals is paramount. Over the years, we’ve received feedback from sponsors and investigators that they were not able to move forward in conducting important clinical investigations where there would be minimal risk as these trials involved situations where obtaining informed consent wasn’t possible, and the agency lacked the authority to permit a waiver of informed consent for that research. With the passage of the 21st Century Cures Act, the FDA’s authorities were changed, allowing greater flexibility. That’s why today, we’re proposing a change to our informed consent regulations in a way that maintains safeguards to protect study participants, while allowing important research to proceed where there is minimal risk to patients,” said FDA Commissioner Scott Gottlieb, M.D. “This change would facilitate the conduct of certain minimal risk clinical investigations that may be important to addressing significant public health needs without compromising the rights, safety, or welfare of human subjects.”

 

''The proposed rule, if finalized, would allow the Institutional Review Board (IRB) responsible for the review and approval of the research to waive or alter certain elements of informed consent, or to waive the requirement to obtain informed consent entirely,''

 

https://www.fda.gov/news-events/fda-brief/fda-brief-fda-takes-steps-allow-greater-flexibility-clinical-investigators-about-informed-consent

Anonymous ID: 0251f9 Feb. 1, 2024, 11:48 a.m. No.20341764   🗄️.is 🔗kun

It took a Great Decpetion to Facilitate The Great Awakening

More & more are Awakening everyday

Heroes are Being Discovered

& Villians Punished

Anonymous ID: 0251f9 Feb. 1, 2024, 11:54 a.m. No.20341788   🗄️.is 🔗kun   >>1792

The Great Awakening is Unstoppable

Morality is Returning to the World

It cannot be Controlled

It cannot be Hindered

 

It is Certian to Happen

& Impossible to avoid