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
Don’t go off this answer wait for confirmation but maybe literacy rate
Answer:
Number 1 should be red because it is a cell
Explanation:
I hope that helped you a little
Answer:
ultra violet radiation (uv rays)
Explanation:
