Read this article to learn about online informed consent training for clinical trials, using a collaborative approach.

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.

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 ...

(AP) – Hospitals must obtain written informed consent from patients before subjecting ... purposes” performed by medical students, nurse practitioners or physician assistants.

The "prudent patient" standard of informed consent focuses on the risks a reasonable person considers when making a decision to undergo treatment. This standard usually requires the testimony of ...