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.

All of Us raises legal questions on consent and DNA privacy as a new federal bill strengthens consumer rights in genomic ...

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The latest word, according to Stat, is that the Department of Health and Human Services directed the CDC to curtail vaccine advertising and focus on informed consent. So, just what does that mean?

The IRB determines, for each protocol it reviews, which of the following elements and disclosures must be included in the informed consent process. Investigators can avoid delay in the review process ...

This article describes how the South supra-region of the NIHR Clinical Research Network developed a collaborative approach to deliver online learning about informed consent for research purposes ...

If appropriate, the child should sign the form and a copy should be given to them ... Investigators should follow the required elements of informed consent when preparing a Parental Consent Form, ...

Obtaining informed consent is more than getting a signature on a form. Informed consent is one of the primary ethical considerations underlying research with human subjects. ALL human subject research ...

Note: Always use lay language that is appropriate to the population being asked to sign the form. Use short paragraphs, bullets and subheadings to increase readability. See the informed consent form ...

This amendment required patients to provide "informed consent" before participating in drug studies. The new standards would go on to change not only the way Americans participated in drug trials ...