Informed consent is one of the most basic aspects of patient-physician relations, as well as subject-researcher relations in the case of research studies. This involves making the patient aware of and verifying that they understand the risks, benefits, facts, and the future implications of the procedure or test they are going to be subjected to.
In the case of genetically modified organisms we have not been made aware of the risks. In fact, the GMO industry has deliberately hidden the real dangers behind the seeds and herbicides they peddle.
The Food and Drug Administration of the United States of America has defined informed consent in the following bureaucratic jargon:
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.
Under all of these definitions, including the exceptions which you can peruse at the above linked official website, what Monsanto is doing with GM crops and their Roundup products are ethically wrong and illegal.
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