Answer:
B), C) and F)
Explanation:
Microeconomics refers to the study of individuals, households, firm behavior for making the decision and distribution of resources. It is useful for the markets that offered goods and services and also handle an individual and economic issues
Therefore in the given case, the microeconomics covered in B, C and F options
Answer: D. Zoning restrictions is not a key success factor in the country location decision.
Explanation: Location of markets, labor productivity and government rules are all very important success factors a company needs to think about before making a decision on which country they want to operate in. The zoning restrictions are not as important because there are usually ways around that by picking a different place in a specific country. The location of markets to buy and sell goods, amount of labor they can expect to be useful and the governments rules on their business are all extremely important.
A Chief Operating Office (COO) is usually considered in the Top level of management of the Executive level of management (these terms can be used interchangeably).
This means that the COO is not usually focused on the day to day operations of organization, but focused on the long-term planning and oversight of the organization.
<span>Mostly seven types of characteristics of information availability enable authorized users or persons or computer systems - to access information without interference, and to receive it in the required format. Well, Accuracy occurs when information is free from mistakes or errors and it has the value that the end user expects.</span>
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.
