Бізнес · 08.09.20141 хв читання
Postmarketing Safety Reports for Human Drug and Biological Products; Electronic Submission Requirements; Corrections
Локальний автоматичний переклад · Оригінальна мова джерела
Короткий зміст
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.