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Testing understanding doesn’t just protect you legally; it builds trust. Patients feel heard and valued when you take the ...
Investigators may request a waiver or alteration of the informed consent process or waiver of consent documentation, provided the conditions described on the waiver form are fulfilled.
The FDA has said the changes will have “benefits in the form of health care advances” because studies that would not have been possible if patient consent were required — can now be done.
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