On the recordNovember 13, 2012
I would like to know what kind of due diligence the FDA has the authority to do?
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congress.govEditor's note · Context
Griffith questions the FDA's oversight and authority regarding compounding practices.
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More from H. Griffith
May 10, 2023
We are also far too dependent on foreign countries for generic drugs and active pharmaceutical ingredients, or API, especially China and India.
Apr 17, 2023
We will focus on three critical areas that are plagued with issues and concerns that we must address moving forward.
Apr 25, 2023
It stands to reason, does it not, that when you limit the number of plans, you create an incentive for price increases.
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