just look it up it will save you time and points Explanation:
Answer:
back in black
ABC by jackson 5
Explanation:
by ACDC that's a good one imo
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
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The information that you have to send to the designated disposal authority is the explanation of the circumstances and regulatory status statement.
<h3>What is the designated disposal authority?</h3>
This is the body that is in charge of disposing obsolete and unserviceable government owned weapons and ammunitions.
An authorized military personnel is the one that can say the state of a waste military material.
Read more on ammunitions here: brainly.com/question/7773692
DDAs provide disposition instructions for excess, obsolete, and unserviceable government-owned ammunition items and components that need to be
Answer:
here
Explanation:
Specialization can help a countries economy by allowing the said country to focus on one low part in the countries economy and improve on that to close in hole allowing its economy to crumble
