Bulk drug registration to file first and review afterward.

Published: 2001-09-11 07:00:00

Updated: 2001-09-11 07:00:00

The registration system for bulk drugs so far required an authorization of their manufacturing license or report for local bulks and a self-product quality control for imported ones, but in the future all bulk drugs either locally producted or imported from overseas shall be registered.

Effective from Jan. 1 next year the KFDA plans to implement the bulk drug registration program initially a...

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