NAPSRX FINAL EXAM TEST BANK SOLVED
QUESTIONS AND VERIFIED RESPONSES
GRADED A+
⩥ What is prohibited by section 503 of the Federal food drug and
cosmetic act as amended by the prescription drug marketing act?.
Answer: The sale, purchase, or trade or offer to sell, purchase, or trade
prescription drug samples.
⩥ Which entity issues monographs that define how drugs should be
stored and what variance is allowed in their states contents?.
Answer: United States Pharmaceutical Convention
⩥ Who regulates the drug sampling for a pharmaceutical
representative?.
Answer: The federal government
⩥ Stores conditions for drug products or based on information supplied
by who?.
Answer: The manufacturer
⩥ In which cases can degraded drugs sometimes still be used?.
,Answer: When the amount of remaining drug has not fallen lower than
85-90% of that stated on the label.
⩥ Drug recalls are almost always negotiated with the FDA before hand..
Answer: True
⩥ What should you do if you receive a shipment from your employer
and you noticed that there are twice as many samples as what is posted
on the packing slip?.
Answer: Call your sales manager to inform them of the mistake and ask
for instructions on proper procedure.
⩥ Which of the following drug R & D has seen the largest cost
increases?.
Answer: Clinical trials
⩥ On average, how long does it take for a new drug to be developed
(from the discovery of the initial compound to FDA approval)?.
Answer: 10-15 years
⩥ Which of the following regulatory agencies is industry based (run
mainly by the companies themselves)?.
Answer: Pharmaceutical Research and Manufacturers of America
, ⩥ The landmark FDA modernization act of 1997 was a major step
forward and enabling safe and effective new drugs and Biologics to be
made available sooner to patients..
Answer: True
⩥ According to your manual which type of system is the best way to
deliver healthcare?.
Answer: A market bases system
⩥ How would increased pharmaceutical price controls affect the US
healthcare system?.
Answer: Increased price controls would stifle innovation.
⩥ What was the intent of the Bayh-Dole act and the Stevenson-Wydler
technology innovation act?.
Answer: To hasten the commercialization of technologies that otherwise
might not be used.
⩥ According to your manual what did the G 10 medicines group recently
report about the pharmaceutical industry in the European Union?.
Answer: There is poor collaboration between publicly and privately
funded research centers.
⩥ What is the aim of preclinical pharmacological studies?.
QUESTIONS AND VERIFIED RESPONSES
GRADED A+
⩥ What is prohibited by section 503 of the Federal food drug and
cosmetic act as amended by the prescription drug marketing act?.
Answer: The sale, purchase, or trade or offer to sell, purchase, or trade
prescription drug samples.
⩥ Which entity issues monographs that define how drugs should be
stored and what variance is allowed in their states contents?.
Answer: United States Pharmaceutical Convention
⩥ Who regulates the drug sampling for a pharmaceutical
representative?.
Answer: The federal government
⩥ Stores conditions for drug products or based on information supplied
by who?.
Answer: The manufacturer
⩥ In which cases can degraded drugs sometimes still be used?.
,Answer: When the amount of remaining drug has not fallen lower than
85-90% of that stated on the label.
⩥ Drug recalls are almost always negotiated with the FDA before hand..
Answer: True
⩥ What should you do if you receive a shipment from your employer
and you noticed that there are twice as many samples as what is posted
on the packing slip?.
Answer: Call your sales manager to inform them of the mistake and ask
for instructions on proper procedure.
⩥ Which of the following drug R & D has seen the largest cost
increases?.
Answer: Clinical trials
⩥ On average, how long does it take for a new drug to be developed
(from the discovery of the initial compound to FDA approval)?.
Answer: 10-15 years
⩥ Which of the following regulatory agencies is industry based (run
mainly by the companies themselves)?.
Answer: Pharmaceutical Research and Manufacturers of America
, ⩥ The landmark FDA modernization act of 1997 was a major step
forward and enabling safe and effective new drugs and Biologics to be
made available sooner to patients..
Answer: True
⩥ According to your manual which type of system is the best way to
deliver healthcare?.
Answer: A market bases system
⩥ How would increased pharmaceutical price controls affect the US
healthcare system?.
Answer: Increased price controls would stifle innovation.
⩥ What was the intent of the Bayh-Dole act and the Stevenson-Wydler
technology innovation act?.
Answer: To hasten the commercialization of technologies that otherwise
might not be used.
⩥ According to your manual what did the G 10 medicines group recently
report about the pharmaceutical industry in the European Union?.
Answer: There is poor collaboration between publicly and privately
funded research centers.
⩥ What is the aim of preclinical pharmacological studies?.
