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;
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Leanne may have Category-specific deficit if she cannot respond to a picture of a spider, a flower, a cat, or her mother.
<h3>What is category-specific deficit?</h3>
Category-specific deficit serves as a deficit whereby one cannot recognize some visual object.
This objects could be animate objects, inanimate and artefacts object.
Learn more about deficit at,:
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