Obtaining the informed consent of a potential human subject for participation in any research (whether an experiment, survey, interview, or demonstration) is a federally mandated safeguard for ...

I ..... son of ..... aged ..... resident of ..... being under the treatment of ..... (state here name of doctor ...

TRICHY: For long, the absence of a uniform template for getting patient consent for medical treatment has been causing confusion among doctors. Addressing the issue, Indian Medical Association (IMA), ...

Background: Consent forms have become too long and often do little to help people understand the risk elements of their participation in research, instead focusing on risk reduction for research ...