Expedited Safety Reporting Requirements for Human Drug and Biological Products; Correction
other · Food and Drug Administration · Rule · Published 1998-03-26 · Effective 1998-04-06 · 63 FR 14611
Document
Document number
98-7833
Federal Register citation
63 FR 14611
CFR reference
21 CFR 314
Type
Rule
Action
Final rule; correction.
Category
other
Sub-agency
Food and Drug Administration
Publication date
1998-03-26
Effective date
1998-04-06
HHS docket
Docket No. 93N-0181
Abstract
The Food and Drug Administration (FDA) is correcting a document that appeared in the Federal Register of October 7, 1997 (62 FR 52237), to include some conforming amendments that were inadvertently omitted. The final rule amended the expedited safety reporting regulations for human drug and biological products. This action is being taken to ensure the accuracy and consistency of the regulations.