Informed consent is vital for any clinical trial. However, the length and complexity of consent information can lead to patients misconstruing key points and failing to understand the implications ...

Informed consent is a foundational element of every clinical trial. Yet, the traditional paper-based process has long been ...

"In addition to clinical consequences, should informed consent include a discussion of the non-medical consequences?" ...

The answer to this inquiry is “yes” — but maybe “no.” Will confidentiality agreements shield any prior art concerns? Once ...

Study results suggest that “telemedicine represents a unique opportunity to reduce time and travel burdens for patients with cancer considering clinical trials,” according to researchers.

Within the context of clinical research, ethics take precedence. Of these, patient autonomy is one of the most basic of ethical principles for decision-making. The query, "What role does patient ...

What are regulatory expectations for distribution of amended Informed Consent Form to the sites?