Challenge: ICH GCP General Questions
Question Number 1

According to ICH GCP when planning trials the sponsor should ensure that sufficient safety and efficacy data from nonclinical studies and/or clinical trials are available to support human exposure to which of the following

  1. the route [of administration]
  2. the dosages
  3. the duration
  4. the trial population

 
A
1 and 2 only
B
2 and 3 only
C
2, 3 and 4 only
D
All of them

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