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DMF re-notification system to take effect from July 1
The drug master file (DMF) system for re-notification of imported raw materials will be implemented from July 1, the Korea Food and Drug Administration said recently.
Under the current regulation, domestic manufacturers are obliged to submit to the KFDA a permit of the original DMF holder in regard to the corresponding raw materials they intend to use.
However, as for the items whose DMF ...
Under the current regulation, domestic manufacturers are obliged to submit to the KFDA a permit of the original DMF holder in regard to the corresponding raw materials they intend to use.
However, as for the items whose DMF ...
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