(a) All information and facts submitted underneath this aspect has to be transmitted to FDA electronically in accordance with § 207.sixty one(a) Except if FDA has granted a ask for for waiver of the need just before the day on which submission of this sort of data is owing. Submission of a request for waiver doesn't excuse well timed compliance To
A registrant who also relabels or repacks a drug that it salvages should checklist the drug it relabels or repacks in accordance with § 207.fifty three rather than in accordance with this portion. A registrant who performs only salvaging with regard to the drug should supply the next listing information and facts for that drug.Glyphosate use is li
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