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KFDA to put human placenta drugs under DMF control.
A human placenta preparation, a popular drug for the treatment of climacteric symptoms, seems to be listed under the DMF (Data master file) control to reinforce its quality controls.
The KFDA announced to disclose "Revised bill for the guideline of bulk drug report" in advance, covering that from July 1 next year the finished placenta preparations should be manufactured with the bulk human ...
The KFDA announced to disclose "Revised bill for the guideline of bulk drug report" in advance, covering that from July 1 next year the finished placenta preparations should be manufactured with the bulk human ...
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