Biology, asked by farizauraku3769, 10 months ago

A food and drug administration rule implemented in december 2000 mandates that any new drug that they intend to be used both by adults and children must undergo pediatric study and that its manufactures list childrens doses on the label.

Answers

Answered by ariaecarg389
0

it will need to undergo for further studies to obtain the best result. the issue here is the human health so it definitely need to be guided and undergo on a long journey of trial for a secure result to prevent conflicts

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