1|Page
CNPR EXAM AND PRACTICE EXAM NEWEST 2025
TEST BANK| COMPLETE 350 REAL EXAM QUESTIONS
AND CORRECT DETAILED ANSWERS (VERIFIED
ANSWERS) GRADED A+ (BRAND NEW!!)
What is a treatment group? - ANSWER - A group of patients assigned to
receive a specified treatment.
What is the main difference between a blinded and a double-blinded
study? - ANSWER - In a double blind study, neither the study staff nor
the study participants know which subjects are in the experimental group
and which are in the control group.
What does asymptomatic mean? - ANSWER - Not exhibiting signs or
symptoms.
What term denotes the study of bodily functions (as opposed to
structures)? - ANSWER - Physiology.
Which of the following is not a type of stem cell
a) multipotent
b) pluripotent
c) semipotent
d) totipotent - ANSWER - Semipotent.
pg. 1
,2|Page
Traditional vaccines are prepared in a number of ways. Which of the
following is not one of them
a) attenuated
b) insulin
c) inactivated
d) toxoids - ANSWER - Insulin
which is not a basic transport mechanism: active transport, homeostasis,
passive diffusion, pinocytosis - ANSWER - homeostasis
the relationship between drug agonists and antagonists - ANSWER -
antagonist and agonists can be used together
the study of effects of movement of drugs in the human body -
ANSWER - clinical pharmacology
what is a common complaint that physicians have about traditional
sampling methods? - ANSWER - drug sample supply is too
unpredictable
what is an entity that is formed by two or more hospitals or other
healthcare entities to negotiate reduced rates with its aggregated
purchasing power? - ANSWER - GPO (Group Purchasing Organization)
another name for a drug derived from a biologic compound - ANSWER
- large molecule
pg. 2
,3|Page
most common policy regarding pharma reps dispensing drug samples in
hospitals? - ANSWER - drug sampling is often forbidden
Which of the following are not types of cytokines
a) interferons
b) interleukins
c) monokines
d) all of these are types of cytokines - ANSWER - All of these are types
of cytokines.
Which of the following is not a type of hormones
a) amino acid derivatives
b) blood glucose
c) polypeptides
d) steroids? - ANSWER - Blood glucose.
When designing and performing clinical trials, several ethical constraints
must be considered. Which one of the following is NOT one of these
ethical restraints
a) geographic variations
b) independent review
c) scientific validity
d) social value? - ANSWER - Geographic variations.
pg. 3
, 4|Page
Which of the following agencies is industry-based (i.e. run mainly by the
companies themselves)?
a) Drug Enforcement Administration
b) European Medicines Agency
c) Pharmaceutical Research and Manufacturers of America (PhRMA)
d) the FDA? - ANSWER - C) PhRMA.
What should be included in the description section of a drug's package
insert information? - ANSWER - The drug's proprietary name and the
established name.
Exclusivity gives exclusive ___________, is granted by the FDA, and
can run concurrently with a patent or not. - ANSWER - Marketing
rights.
What differentiates exclusivity from a patent? - ANSWER - Exclusivity
is only granted upon the drug's FDA approval.
What is required of an invention for it to be worthy of patent protection?
- ANSWER - It must be novel, useful, and not obvious.
A generic drug is ________ to the originator brand-name drug in dosage,
strength, safety, and equality. - ANSWER - bioequivalent
The FDA's Criteria for Equivalency requires the drugs contain identical
amounts of the same inactive ingredients. - ANSWER - True
pg. 4
CNPR EXAM AND PRACTICE EXAM NEWEST 2025
TEST BANK| COMPLETE 350 REAL EXAM QUESTIONS
AND CORRECT DETAILED ANSWERS (VERIFIED
ANSWERS) GRADED A+ (BRAND NEW!!)
What is a treatment group? - ANSWER - A group of patients assigned to
receive a specified treatment.
What is the main difference between a blinded and a double-blinded
study? - ANSWER - In a double blind study, neither the study staff nor
the study participants know which subjects are in the experimental group
and which are in the control group.
What does asymptomatic mean? - ANSWER - Not exhibiting signs or
symptoms.
What term denotes the study of bodily functions (as opposed to
structures)? - ANSWER - Physiology.
Which of the following is not a type of stem cell
a) multipotent
b) pluripotent
c) semipotent
d) totipotent - ANSWER - Semipotent.
pg. 1
,2|Page
Traditional vaccines are prepared in a number of ways. Which of the
following is not one of them
a) attenuated
b) insulin
c) inactivated
d) toxoids - ANSWER - Insulin
which is not a basic transport mechanism: active transport, homeostasis,
passive diffusion, pinocytosis - ANSWER - homeostasis
the relationship between drug agonists and antagonists - ANSWER -
antagonist and agonists can be used together
the study of effects of movement of drugs in the human body -
ANSWER - clinical pharmacology
what is a common complaint that physicians have about traditional
sampling methods? - ANSWER - drug sample supply is too
unpredictable
what is an entity that is formed by two or more hospitals or other
healthcare entities to negotiate reduced rates with its aggregated
purchasing power? - ANSWER - GPO (Group Purchasing Organization)
another name for a drug derived from a biologic compound - ANSWER
- large molecule
pg. 2
,3|Page
most common policy regarding pharma reps dispensing drug samples in
hospitals? - ANSWER - drug sampling is often forbidden
Which of the following are not types of cytokines
a) interferons
b) interleukins
c) monokines
d) all of these are types of cytokines - ANSWER - All of these are types
of cytokines.
Which of the following is not a type of hormones
a) amino acid derivatives
b) blood glucose
c) polypeptides
d) steroids? - ANSWER - Blood glucose.
When designing and performing clinical trials, several ethical constraints
must be considered. Which one of the following is NOT one of these
ethical restraints
a) geographic variations
b) independent review
c) scientific validity
d) social value? - ANSWER - Geographic variations.
pg. 3
, 4|Page
Which of the following agencies is industry-based (i.e. run mainly by the
companies themselves)?
a) Drug Enforcement Administration
b) European Medicines Agency
c) Pharmaceutical Research and Manufacturers of America (PhRMA)
d) the FDA? - ANSWER - C) PhRMA.
What should be included in the description section of a drug's package
insert information? - ANSWER - The drug's proprietary name and the
established name.
Exclusivity gives exclusive ___________, is granted by the FDA, and
can run concurrently with a patent or not. - ANSWER - Marketing
rights.
What differentiates exclusivity from a patent? - ANSWER - Exclusivity
is only granted upon the drug's FDA approval.
What is required of an invention for it to be worthy of patent protection?
- ANSWER - It must be novel, useful, and not obvious.
A generic drug is ________ to the originator brand-name drug in dosage,
strength, safety, and equality. - ANSWER - bioequivalent
The FDA's Criteria for Equivalency requires the drugs contain identical
amounts of the same inactive ingredients. - ANSWER - True
pg. 4
