QQuestion
Question
The investigator must report adverse events to the:
A. Subject
B. Sponsor
C. FDA
D. IRB only
6 months agoReport content
Answer
Full Solution Locked
Sign in to view the complete step-by-step solution and unlock all study resources.
Step 1Let me solve this research ethics problem systematically:
Step 2: Understand the Context
This question relates to reporting adverse events in clinical research, which involves understanding the responsibilities of an investigator when unexpected or harmful events occur during a research study.
Final Answer
IRB only The IRB is the primary oversight body responsible for protecting human subjects and must be immediately informed of any adverse events that could impact participant safety or study integrity.
Need Help with Homework?
Stuck on a difficult problem? We've got you covered:
- Post your question or upload an image
- Get instant step-by-step solutions
- Learn from our AI and community of students
Related Questions
No related questions found