Topics: CLPT, M.Pharmacy, Pharmaceutics; Regulatory Affairs Quiz
An IMPD should not include summaries of information related to the quality, manufacture, and control of the IMP.
A. TRUE
B. FALSE
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The IB also provides insight to support the clinical management of the trial ……………… during the course of the clinical trial.
A. Applicant
B. Sponsor
C. Investigator
D. Subjects