To incentivize more outsourcing facilities to compound drugs that are in shortage, the US Food and Drug Administration needs to provide greater regulatory transparency by finalizing its bulk drug compounding list and issuing final good manufacturing practice regulations for these facilities, according to a recent report from the Pew Charitable Trusts.
While the coronavirus pandemic has prompted the agency to loosen restrictions against compounding some shortage-prone drugs for emergency use, what is less clear is what will happen after the
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