What Is The Process For Submitting A DMF In Korea?

To submit a Drug Master File (DMF) in Korea, prepare the required documentation, including detailed information on Active Pharmaceutical Ingredients (APIs), Excipients, or Packaging Materials. Submit the DMF to the Ministry of Food and Drug Safety (MFDS) through their electronic submission system. Ensure compliance with Korean regulations and respond promptly to any MFDS queries or requests.

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