Study online at https://quizlet.com/_cjoj9y
1. Clinical trials designed to meet regulatory approval criteria are conducted to
do all of the following. Choose all that apply: -guarantee that the drug/device is tolerated, safe,
and effective
-ensure the safety and efficacy of a medical strategy
-explore how a drug or device interacts with the physiology of the human body
2. Which type of study can determine a cause-effect relationship?: Randomized con-
trolled trials
3. What is the integration of best research evidence with clinical expertise and
patient values?: Evidence-based medicine
4. TRUE/FALSE Medical writers should have a strong understanding of literature
searching.: True
5. What are individual board members also known as?: Advisors
6. Larger companies may split the role of the MSL to account for different
functions related to how the organization interacts with KOLs.: TRUE
7. A Pharma company is looking to begin the development of a new drug. Why
would the company consult an advisory board?: To provide their opinion on the research and
development of the drug
8. TRUE/FALSE Standard Response Documents (SRDs) are prepared only for
HCPs in response to questions about product(s): FALSE
9. What type of FDA-mandated studies are most common? Select the best an-
swer: Randomized Controlled Trials (RCTs)
10. Dr. Simpson, a neurologist, occasionally participates on an advisory board
for Lightning Pharmaceuticals. Dr. Simpson has also just become a member of
a national committee that makes recommendations for clinical guidelines and
formulary decisions. Is Dr. Simpson required to disclose her relationship with
Lightning Pharmaceuticals to the national committee she is a member of?: Yes,
it would be unethical and potentially a conflict of interest if she does not disclose the relationship
11. TRUE/FALSE Post-Marketing studies are only conducted on newly-approved
drugs.: FALSE
12. Which of the following provides best practice and ethical standards for
reporting research published in medical journals?: ICMJE
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