Trusted Resources: Education
Scientific literature and patient education texts
Informed Consent for Clinical Trials
source: U.S Food & Drug Administration
year: 2018
summary/abstract:The term informed consent is mistakenly viewed as the same as getting a research participant’s signature on the consent form. FDA believes that obtaining a research participant’s verbal or written informed consent is only part of the process.
Informed Consent Involves Providing a Potential Participant With:
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