The governing body in an institution that is responsible for approving all research.

The location of unethical studies performed on syphilis patients

The ethical principle that allows patients to make their own decisions regarding treatments

The purpose of the Institutional Review Board

Establishes that respecting and doing what's right for the patient is the most important thing in research, above all else

The ethical principle of not inflicting harm

The document the IRB uses to determine the nature of the research and what will happen to the research subjects in the study

Outlines the basic provisions for the IRB, informed consent and Assurances of Compliance in the US

Summarizes ethical principles and guidelines for research involving human subjects

The type of review needed for a research study that involves minimal risk

A standard for the design, conduct, performance, auditing, monitoring, recording, analyses and reporting of clinical trials

The practice of including all data, rather than selecting cases with data supporting the desired outcome

The document that explains to a potential research participant the purpose and potential risks and benefits of participation in the study

Established that research likely to result in death or disabling injury should not be done

Reporting data that is incomplete, mishandling specimens, poor record-keeping, and deleting data that does not support the hypothesis