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

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.

This event is co-sponsored by the Korea Pharmaceutical Association (KPA) and the Korea Pharmaceuti...