Topics: CLPT, M.Pharmacy, Pharmaceutics; Regulatory Affairs Quiz
Generally, the ……………….. is responsible for ensuring that an up-to-date IB is made available to the investigator(s).
A. IRB
B. USFDA
C. sponsor
D. Trail subject
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‘IB’ do not contain Physical, Chemical, and Pharmaceutical Properties and Formulation, details.
A. TRUE
B. FALSE