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.

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 ...

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 ...