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

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 informed consent process is an ethical and legal requirement ... Many times, it is even the neighbour (a hospital attendant posing as a 'nurse') that gives them the injections.

Prior to the vote on the Senate floor, Sen. Andre Jacque, R-New Franken, one of the bill’s cosponsors, said the bill will ...

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.

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.

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 ...