In event of the evaluation of unanticipated adverse device effects, they must be reported to the FDA by the sponsor.
What is the FDA?
The FDA is the acronym for the Food and Drug Administration. This agency is in charge of the process of production and approval of foods and drugs in the United States.
In event of the evaluation of unanticipated adverse device effects, they must be reported to the FDA by the sponsor.
Learn more about FDA:https://brainly.com/question/9072310
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