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A registrant who also relabels or repacks a drug that it salvages should record the drug it relabels or repacks in accordance with § 207.fifty three rather than in accordance with this section. A registrant who performs only salvaging with regard to your drug need to deliver the next listing data for that drug.On top of that, GRAS uses need to ful
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(a) All facts submitted underneath this aspect need to be transmitted to FDA electronically in accordance with § 207.61(a) unless FDA has granted a ask for for waiver of this need before the date on which submission of this kind of information and facts is due. Submission of the request for waiver doesn't justification well timed compliance Along
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