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Achieving informed consent requires a potential contributor to be in possession of sufficient knowledge about our plans for a reasoned decision to take part in our content. The Editorial Guidelines ...

Although informed consent for clinical treatment has become a vital part of contemporary medical practice, it means different things in different contexts (Figure 1), is variably practised and rarely ...

Ali Hussain has a background that consists of a career in finance with large financial institutions and in journalism covering business. Michael Boyle is an experienced financial professional with ...

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 ...

Under Colorado law, students under the age of 18 who receive medical treatment at Wardenburg Health Center must first have a parent or guardian sign the Parental/Guardian Consent for Treatment of a ...

The Orissa high court has ordered authorities to revise the APAAR ID consent form. The court observed the current format lacks a clear option for parents to refuse or opt out of the voluntary scheme, ...

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.