standards for consent and standards for using humans as test subjects have not been explained to the public. Institutional Review Boards (IRBs) and Protection of Human Subjects in Clinical Trials Electronic Code of Federal Regulations: §50.20 General requirements for informed consent. After reading about the way the Covid vaccine has been engineered to evade the body's natural immune system and to also cause the vaccinated to transmit the virus. It suddenly occured to me that this could be Satan's means to devour the man-child. Which means our rescue (rapture) is very soon. Amen. Again, every indication is that we are more near than far! Let it be soon! Indeed, Summer is near! Summer in Heaven, how lovely that would be! TR Excellent thought Rick....it very well could be, let's go home!!
Except as provided in §§50.23 and 50.24, no investigator may involve a human being as a subject in research covered by these regulations unless the investigator has obtained the legally effective informed consent of the subject or the subject's legally authorized representative. An investigator shall seek such consent only under circumstances that provide the prospective subject or the representative sufficient opportunity to consider whether or not to participate and that minimize the possibility of coercion or undue influence. The information that is given to the subject or the representative shall be in language understandable to the subject or the representative. No informed consent, whether oral or written, may include any exculpatory language through which the subject or the representative is made to waive or appear to waive any of the subject's legal rights, or releases or appears to release the investigator, the sponsor, the institution, or its agents from liability for negligence.
