KFDA Attempts to Bring Out Industry-Wide Understanding on DMF Requirements

Published: 2005-01-10 07:00:00

Updated: 2005-01-10 07:00:00

Reflecting the government's effort to implement the Pharmaceutical Bulk Report System scheduled by September of this year, the Korea Food and Drug Administration (KFDA) will host a meeting on January 12th to provide discussion and explanation sessions on the Drug Master File (DMF) requirements.
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