Answer:
The answer to the following question is the option "B".
Explanation:
The term REA stands for Resources, events, agents. It is a model that provides us an accounting system. In this system, we can re-engineer for the computer age and Integrate separate REA diagrams for individual or a comprehensive organization.  This process does not affect any event and agents who participate in events affecting shared resources. So the answer to this question is "none of the other entities".
 
        
             
        
        
        
Answer:
Explanation:
A credit is a financial transaction where someone takes a loan for a certain amount of money to another person, and this another must pay this money in a period of time, determinate from both parts, in this case, a country can get a credit, if this country pay this debt, the country will have a good record, and they can to ask another credit, but if they don't pay, the debt will be bigger.
 
        
             
        
        
        
e. /Users/me/Documents/file.txt
 
        
             
        
        
        
An IND Safety Report would be most likely filed by the sponsor with the FDA for the observations associated with: subject 603 only.
<h3>What is FDA?</h3>
FDA is an abbreviation for Food and Drug Administration and it can be defined as a federal agency of the government of the United States of America that is saddled with the responsibility of protecting the consumers of drugs and other edible products from hazards (poisons), as well as promoting and enhancing public health safety.
<h3>What is an 
IND Safety Report?</h3>
IND Safety Report is a short terminology for Investigational New Drug Safety Report and it can be defined as any findings from tests that are conducted in the laboratory on animals which suggest a significant risk for human subjects, when the drug is used.
Based on the information provided, we can reasonably infer and logically deduce that an Investigational New Drug (IND) Safety Report would be most likely filed by the sponsor with the Food and Drug Administration (FDA) for the observations associated with subject 603 only because it  suggest a higher and significant risk for human subjects.
Read more on IND Safety Report here: brainly.com/question/28084797
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