Postmarketing Safety Reports for Human Drug and Biological Products; Electronic Submission Requirements; Corrections

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The Food and Drug Administration (FDA) is correcting a document entitled "Postmarketing Safety Reports for Human Drug and Biological Products; Electronic Submission Requirements; Correction" that appeared in the Federal Register of August 14, 2014 (79 FR 47655). The document published without the required RIN number and in the Notice category. This document corrects those errors.