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.

Warning! Sweeping changes in public health are on the rise. The latest word, according to Stat, is that the Department of ...

The failure of Panhandle Health District board members to honestly address how patients are informed of the risks and benefits of vaccine products at the March 3 PHD meeting reveals a troubling ...

This is a requirement for studies meeting the definition of a clinical trial and funded by ... party and must ensure compliance with the posting requirement. The informed consent form must be posted ...

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 ...

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 ...