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KFDA publish Site Master File
The Korea Food and Drug Administration said it has published Site Master File, a GMP (Good Manufacturing Practice) related manual of individual medicines on manufacturing site.
The drug agency said the manual covers a format for site master file, review and approval of GMP report, production and test control and in-house inspections.
KFDA said the manual will standardize GMP documents int...
The drug agency said the manual covers a format for site master file, review and approval of GMP report, production and test control and in-house inspections.
KFDA said the manual will standardize GMP documents int...
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