Prior to the vote on the Senate floor, Sen. Andre Jacque, R-New Franken, one of the bill’s cosponsors, said the bill will ...

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.

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 informed consent explains the nature of psychiatric services provided, your rights and responsibilities, confidentiality, and how your health insurance will be utilized. Your understanding and ...

The Israeli Privacy Protection Authority (PPA) has issued a new statement introducing a significant change in the interpretation of the law and in ...

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 ...

He’s also an expert on informed consent. “An individual that’s enrolled in a clinical trial should know the potential benefits and the potential risks,” he said. “So informed consent ...

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?

These enhanced protections involved changes to the consent process. The informed consent requirements introduced via the Revised Common Rule are listed below. These requirements apply to the following ...

Kennedy wants future vaccine communications to focus on “informed consent,” by which he means giving people information about the adverse events associated with vaccines. That’s a distorted ...

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 of ...

Use short paragraphs, bullets and subheadings to increase readability. See the informed consent form template (pdf) for more help and sample language. 1. Title of the Study 2. Names and Affiliations ...