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KFDA to mull over how to treat unacceptable bulk drugs
The KFDA seems to be in anguish how to treat an unacceptable bulk drug with reference to the DMF, a bulk drug master file report system, which is still being reviewed on ongoing receit of its submission from the bulk suppliers.
The KFDA said that about 40% of the DMF was completed to review, facing difficulties how to handle some unacceptable bulk drugs. These bulk drugs showed quality prob...
The KFDA said that about 40% of the DMF was completed to review, facing difficulties how to handle some unacceptable bulk drugs. These bulk drugs showed quality prob...
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약업닷컴의 모든 컨텐츠는 저작권법의 보호를 받습니다. 무단 전재⋅복사⋅배포 등을 금합니다.