IRB — Perfunctory Review
Institutional Review Boards Perfunctory Review Process,
Evidence-Based Validation of the AHRP Mission for Disclosure & Voluntary, Informed,Consent
“Nothing is more fundamental to the ethical conduct of clinical trials than the informed consent of research participants. The Nuremberg Code and every subsequent major international statement about ethics and medical research enshrine this role.” In his recent article in Science and Engineering Ethics, Dr. Mark Yarborough, Dean’s Professor of Bioethics at the University of…
Read MoreUCSD Researchers Disregard Human Subject Protections
Millions of people around the world participate in research trials each year, whether for personal, financial or humanitarian reasons. They submit their DNA, organs, body chemistry or personal history to studies that aim to better society. A substantive investigative news report by San Diego’s independent investigative news source, Inewsource.org by Brad Racino and Jill Castellno,…
Read MoreResearch Uproar: Cancer Clinic Investigation Broad Implications
…instead of informed patient consent, doctors too often promoted trial treatments as superior to standard approaches, even when there was no supporting evidence.
Read MoreIndia: Guinea Pig to the World_Wired Mag
The pharmaceutical industry’s dilemma: there are few volunteers in the drug-consuming prosperous countries–so they have taken half their business to underdeveloped countries.
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