KFDA clarifies bioequivalence testing on transdermal drugs

Published: 2010-06-24 06:57:00

Updated: 2010-06-24 06:57:00

The Korea Food and Drug Administration has unveiled its policy on the bioequivalence testing of oral transdermal medicines in a form of question and answer (Q/A).

The Q/A describes comparative disintegration test and its validation, including precipitation in the comparative disintegration.

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