The descriptions of 2,940 active ingredients will be standardized to avoid that they are misunderstood as other chemical substances in the screening process for approval, according to the Korea Food and Drug Administration.
Under the proposed guideline, ‘diisopropylethylamine (DIPEA) may be described as 'diisopropylethylamine’ only in Korean.
The names of in vitro diagnostics may be used ...
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