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KFDA to overhaul duplicate API management system
The Korea Food and Drug Administration is considering ameliorating the current double management system of active pharmaceutical ingredients (API).
The drug agency is attempting to integrate both the drug master file (DMF) management system and previous GMP inspection for raw materials into the one system for efficient management.
The KFDA also plan to expand the DMF coverage to all APIs ...
The drug agency is attempting to integrate both the drug master file (DMF) management system and previous GMP inspection for raw materials into the one system for efficient management.
The KFDA also plan to expand the DMF coverage to all APIs ...
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