Answer:
agree with this
.................................
The condition will be excused because of ESTOPPEL. Estoppel is an obstruction which prevents a person from asserting a right or denying a fact. The obstruction is normally due to the person action, conduct or failure to act. The principal aim of estoppel is to prevent injustice due to inconsistency or fraud. Estoppel is of two types: equitable and legal estoppel.
Risk that are caused by the response to the another risk is known as secondary risk. The first option is correct.
<h3>What are risk?</h3>
Risk refers to the possibility of the danger or harm. For example there is risk involved to change the career. The risk taken can lead to any outcome it can be positive or negative.
There are various kinds of risk one of those kind is the secondary risk in which the risk is taken as a result of the previous actions taken to deal with the situation.
Thus the correct option is Secondary risk.
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Answer:
Earnings per share (EPS) = $0.71 per share
Explanation:
The earnings per share is a metric used by investors in deciding their investment decisions and it is also used as a metric to calculate the corporate value. The earnings per share simply tells the net income earned per each of the common share outstanding. The formula for earnings per share is,
Earnings per share (EPS) = (Net Income - Preferred dividends) / Weighted-average common shares outstanding
Earnings per share (EPS) = (213 - 0) / 300
Earnings per share (EPS) = $0.71 per share
One of the phases of drug development is the post-marketing surveillance phase. Report adverse effects to FDA, is the activity carried out during this phase
This is further explained below.
<h3>What is drug development?</h3>
Generally, Medicine development is the method of getting a novel pharmaceutical product onto the market after identifying a lead chemical via drug discovery and development.
In conclusion, The post-marketing monitoring phase is one of the stages that are included in the medication development process. Notifying the FDA of any unintended consequences is the action that is carried out at this phase.
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complete question
One of the phases of drug development is the post-marketing surveillance phase. Which activity is carried out during this phase?
Health care providers report adverse effects to FDA.
Healthy volunteers are involved in the test.
In vitro tests are performed using human cells.
The drug is given to clients with the disease.
