Ethics in International Affairs IRL4527 L, Adibayeva Aigul

the clinical usefulness of information, e.g. for making decisions concerning diagnosis, prevention, or treatment.

using force, threats, or intimidation to make a person comply with a demand. 

an agreement between two or more collaborating research groups concerning the conduct of research. The agreement may address the roles and responsibilities of the scientists, access to data, authorship, and intellectual property.

the process of developing and marketing commercial products (e.g. drugs, medical devices, or other technologies) from research. See also Copyrights, Intellectual Property, Patents.

a body of law based on judicial decisions and rulings.

The U.S. Department of Health and Human Services regulations (45 CFR 46) for protecting human subjects, which has been adopted by 17 federal agencies. The Common Rule includes subparts with additional protections for children, neonates, pregnant women and fetuses, and prisoners.

a process for involving a community in the review of research conducted on members of the community. Some research studies include community advisory boards as a way of involving the community.

 the legal right to make decisions for one’s self. Adults are considered to be legally competent until they are adjudicated incompetent by a court. See Decision-making capacity.

in research, complying with laws, institutional policies and ethical guidelines related to research.

Action or behavior. For example, conducting research involves performing actions related to research, such as designing experiments, collecting data, analyzing data, and so on.