Exam (elaborations)
BCMAS QUESTIONS AND ANSWERS
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BCMAS QUESTIONS AND ANSWERS
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Name: Score:282 Multiple choice questions
Term 1 of 282
What best describes retrospective data?
it is used to estimate costs of the present year
it describes data that is gathered in real-time
it refers to data collected for future projections
it is information used solely for marketing strategies
Term 2 of 282
Most commonly used study design:
perpendicular
harmonization
cluster randomization
parallel
Term 3 of 282
What are the most common discount rates?
5-10%
3-5%
1-3%
1-2%
,Term 4 of 282
REMS are designed to address the _________ for different drugs and classes of drugs.
Safety strategies
Unique safety measures
Sales and distribution
Many safety measures
Term 5 of 282
What section of Title 21 of the Code of Federal Regulations (21 CFR) provides the procedures
for performance standards development?
21 CFR 861
21 Cfr 999
21 Cfr 632
21 Cfr 512
Term 6 of 282
21 CFR Part 56
IRB
A, B
ETHICS
FDA
Term 7 of 282
When looking for research opportunities, you can use some Internet resources, such as:
nspires
grants.gov
sam.gov
research.gov
,Term 8 of 282
What are bibliometrics designed to provide?
tools for tracking social media engagement
strategies for increasing publication frequency
methods for evaluating product sales
shortcuts for assessing impact through measuring citations
Term 9 of 282
T/F: The use of storytelling in the MSL/HCP interaction is outdated and should be avoided.
True
False
Term 10 of 282
T/F: Primary literature is original research.
True
False
Term 11 of 282
At what point in the drug development process can a product launch occur?
clinical trials
preclinical development
synergy
regulatory approval
, Term 12 of 282
Which statements about generic drugs are true? Select all that apply.
The quality must be the same as the comparable brand name drug.
They must demonstrate greater safety than the comparable brand name drug.
The dosage form must be the same as the comparable brand name drug.
The strength must be lower than the comparable brand name drug.
The intended use must be the same as the comparable brand name drug.
Term 13 of 282
In what year were the first GPP guidelines published?
1998
1993
2002
2003
Term 14 of 282
Individual board members are known as:
active members
future
consultants
advisors
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