Using credit allows you to make impulsive buys - this is not a benefit to using credit instead of cash. It is never good to make impulsive buys, you just waste money on something that you usually don't even need.
Answer: what is not true about Allowance for doubtful accounts is that ----It is a liability account
Explanation:
Allowance for doubtful accounts is a contra-asset account that shows only amounts expected to be paid by negating the total receivables recorded on the balance sheet.
The allowance for doubtful accounts is credited when bad debts expenses are recorded and debited when uncollectible accounts are written off.
In summary, Allowance for doubtful accounts estimates the amount of accounts receivable expected but will not be paid by customers.
Answer:
Shows the time an employee worked on each job, the pay rate, and the total cost chargeable to each job.
Explanation:
A time ticket is a document that constitutes of the working period of the particular employee. It includes the working period for which the employee has been paid by the company. It constitutes of the initial time of the working day and the ending time of the day. The work hour for which the employee is paid and the cost invoked during the course of the period is also listed in the time ticket.
The answer is: LARGER parietal lobes
Parietal lobe is a part of our brain which function is to integrating our sensory input with our visual system.
Larger parietal lobes will grant us the capability to do fast analyzation on complicated matters while using our visual to arrange the structure at the same time, which will be really useful for a computer engineer.
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.
