Informed consent is one of the primary requirements of research involving human participants. It is important to remember that informed consent is an ongoing process, not a document or single event.

Using this standard, informed consent remains focused on what information a reasonable person would want to have to make an informed choice about participation; this includes: the nature of the ...

and One of the following statements about any research that involves the collection of identifiable private information or identifiable biospecimens: In seeking informed consent, the following ...

Investigators should follow the required elements of informed consent when preparing ... the risk and anticipated benefit to the research subjects, and the child’s age, maturity, status, and condition ...

The Forms and Templates page includes templates for informed consent documents. However, because each human participants research (HSR) proposal is different and carries unique risks to participants, ...

See the informed consent form template (pdf) for more help and sample language ... to the subject and their probability as a direct result of participation in the research and/or from breach of ...

Furthermore, unless the consent process has been specifically waived by the IRB, no subjects may be included in research unless the investigator has obtained the legally effective informed consent ...