Exam (elaborations)
BCMAS STUDY QUESTIONS AND ANSWERS
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BCMAS STUDY QUESTIONS AND ANSWERS
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Name: Score:20 Multiple choice questions
Term 1 of 20
During the publication workflow, the medical director has analyzed the data to determine
informational gaps and has determined the scientific communication platform. The medical
director has determined they do not have enough data to support their scientific
communication points. What should happen next in the process?
Initiate A Publication plan
Conduct Phase IV studies
Document the agreement
Submit the data to a peer-reviewed journal
Term 2 of 20
Which statement is true about public pharmaceutical companies?
They can only sell products within their home country
They are prohibited from advertising their products to consumers
They are required to release information detailing how they will commercialize their
product
They must keep all product information confidential from the public
,Term 3 of 20
Which of the following are primary pharmaceutical regulators in the United States? Check all
that apply.
Sales and marketing strategies
Measurable
Specific
Relatable
· All authors and contributors should disclose any relationships or potential competing
interests relating to the research
Department of Justice (DoJ)
Food and Drug Administration (FDA)
Term 4 of 20
True/False Publications play a vital role in generating important information for HCPs.
True
False
Term 5 of 20
What type of manufacturers conduct research and manufacture drugs under licenses from
other companies?
CRAMS (Contract Research and Manufacturing Services)
Sales and marketing strategies
Harmonization
Conduct phase iv studies
, Term 6 of 20
What are bibliometrics designed to provide?
· surveys to gather patient feedback on medication effectiveness
· Shortcuts for assessing impact through measuring citations
· Comprehensive reviews of all published medical literature
· detailed analysis of drug pricing strategies
Term 7 of 20
When first working on a publication, what should authors do to identify their rights, roles, and
responsibilities?
The medical director
Document the agreement
Avoid disclosing the funding source
Harmonization
Term 8 of 20
The process of international cooperation, coordination, and common standards across the
global pharmaceutical industry is referred to as:
Formulation
Harmonization
The Medical Director
Pharmacovigilance
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