Evaluation of unanticipated adverse device effects (UADDEs) must be reported to the FDA by the IRB and all investigators participating in the test of the product within ten working days.
<h3>What is IRB and FDA?</h3>
The full meaning of IRB is Institutional Review Board, while the full meaning of FDA is the United States Food and Drugs Administration - a Federal Agency.
The above bodies are responsible for protecting American citizens from harmful products.
Learn more about FDA and IRB at;
brainly.com/question/17432443
#SPJ11
The answer should be William R king
Answer:
C
Explanation:
Because I know this answer bc i legit just had it
Answer:
B
Explanation:
the journalistic approach
A journalistic approach to content marketing gives people what they want by recognising this need, and capitalising on it without cynicism.
