Answer:
1. Deontology C. is the normative ethical theory that a moral act is based on whether the act itself is right or wrong under a series of rules, and not based on the consequences of the act.
2. Utilitarianism D. the best ethical choice produces the best result for the greatest number
3. Free market ethics A. goods and services are worth what people believe they are worth and are willing to pay for and businesses need only be concerned with making a profit for owners (shareholders)
4. Virtue ethics B. based on the moral character of the person rather than the act
I would assume it’s A.
A business cannot function without information stored for later analysis when necessary.
Answer:
use a combination of tests measuring both cognitive abilities and non-cognitive traits such as emotional intelligence and personality
Explanation:
In the given scenario many of the applicants Fran perceives as having good emotional intelligence and agreeable personalities (a plus for a fitness studio), do not score well on the cognitive ability test.
Since she wants people that have non-cognitive traits such as emotional intelligence and personality, and also good cognitive abilities.
She will need to use a combination of tests measuring both cognitive abilities and non-cognitive.
Hey!
The National Banking Acts gave the federal government three important powers:
The power to charter banks
The power to require banks to hold adequate gold and silver reserves to cover their bank notes
The power to issue a single national currency
Hope this helps! :)
Answer:
Investigators should let the subjects know in the informed consent form that the monitor, auditor, IRB/IEC, and the regulatory authorities may be privy to the subject's medical records.
Explanation:
FDA stands for Food Drug and Administration that see to the regulation of food and drug in The U.S.
ICH E6 is an international ethical and scientific quality standard for designing, conducting, recording and reporting trials that involve the participation of human subjects. These guidelines are meant for standard practice globally.
Investigators should let the subjects know in the informed consent form that the monitor, auditor, IRB/IEC, and the regulatory authorities may have access to the subject's medical records. Failure to do so is unethical and Subjects can pick up a case on this at the law court.
