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SOCRA Certified Clinical Research Professional (CCRP) CCRP Question # 38 Topic 4 Discussion

SOCRA Certified Clinical Research Professional (CCRP) CCRP Question # 38 Topic 4 Discussion

CCRP Exam Topic 4 Question 38 Discussion:
Question #: 38
Topic #: 4

An investigator reports a serious adverse event suspected to be drug-related. By CFR, the sponsor must notify FDA no later than:


A.

1 day


B.

7 days


C.

10 days


D.

15 days


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