Keynesians agree with the above statement, but monetarists do not.
Answer: Option D
<u>Explanation:</u>
Monetary policy is nothing but a policy followed by the central bank or any other banking agencies' authorities. As they can include control of money supply and interest rate that in turn helps the government to create growth in economic.
Keynesians also believe in the fact money supply has some relation with the growth f the country’s economy. They literally don’t mind about the rate of interest and the time provided to it. But Monetarists strongly believe in controlling the money in the economy.
Answer:
local option
Explanation:
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Answer:
The thick mud felt as if-<u>dirt got wet</u>
Answer:
An institutional review board (IRB), also known as an independent ethics committee (IEC), ethical review board (ERB), or research ethics board (REB), is a type of committee that applies research ethics by reviewing the methods proposed for research to ensure that they are ethical.
Explanation:
- Conducting initial and continuing review of research;
- Reporting findings and actions to the investigator and the institution;
- Determining which projects require review more often than annually;
- Determining which projects need verification from sources other than the investigator that no material changes have occurred since previous IRB review;
- Ensuring prompt reporting to the IRB of proposed changes in a research activity, and ensuring that changes in approved research, during the period for which IRB approval has already been given, may not be initiated without IRB review and approval except where necessary to eliminate apparent immediate hazards to the human subjects;
- Ensuring prompt reporting to the IRB, appropriate institutional officials, any department or agency head and OHRP for research conducted or supported by HHS, and the FDA for FDA-regulated research of:
- Any unanticipated problems involving risks to human subjects or others;
- Any instance of serious or continuing noncompliance with the applicable HHS and FDA regulations or the requirements or determinations of the IRB; Any suspension or termination of IRB approval.
HHS and FDA regulations do not provide additional detail on the content of IRB written procedures, which gives IRBs the flexibility to establish procedures best suited to their own operations.
