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UPS Healthcare November Lexicon Quiz

A visually engaging image depicting pharmaceutical and medical device compliance, featuring symbols of law, healthcare, and research.

UPS Healthcare November Lexicon Quiz

Test your knowledge on key terms and regulations within the pharmaceutical and medical device industry with our engaging quiz!

Challenge yourself and learn more about:

Consent Decree
Form 483
Institutional Review Boards

4 Questions1 MinutesCreated by RegulatoryEagle42

A Consent Decree is the ultimate legal action which may be taken by FDA on pharma and med device companies who have not heeded warning letters. It is the ultimate failure on the part of manufacturers to uphold quality and compliance with GMP. True or false?

True

False

Form 483 is issued when an investigator has observed any conditions that in their judgment may constitute violations of the Food Drug and Cosmetic (FD&C) Act. True or false?

True

False

An IRB is any board, committee or other groups formally designated by the government to review, to approve the initiation of, and to conduct periodic review of, biomedical research involving human subjects. True or false?

True

False

What does IRB stand for?

Institutional Referral Board

Intentional Revenue Body

Institutional Review Board

Institutional Review Body

Intentional Referral Body

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