Clinical trials regulations

| June 19, 2015

Clinical trials regulations

The current tendency is to provide subjects for clinical trials with very detailed informed consent documents, some of which can run to 15 pages and contain fairly technical medical terms. Some of these informed consent documents are probably only poorly understood by potential subjects and may even scare some subjects away. Which do you think would be a better policy – the current policy of being totally transparent and providing detailed information to potential subjects, or a policy of providing less, but perhaps more understandable, information. Explain why you feel one or the other policy would be better.
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