
[Federal Register Volume 79, Number 175 (Wednesday, September 10, 2014)]
[Proposed Rules]
[Page 53670]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2014-21481]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

21 CFR Parts 610 and 680

[Docket No. FDA-2014-N-1110]


Revocation of General Safety Test Regulations That Are 
Duplicative of Requirements in Biologics License Applications; 
Correction

AGENCY: Food and Drug Administration, HHS.

ACTION: Proposed rule; correction.

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SUMMARY: The Food and Drug Administration is correcting a proposed rule 
entitled ``Revocation of General Safety Test Regulations That Are 
Duplicative of Requirements in Biological License Applications'' that 
appeared in the Federal Register of August, 22, 2014. The document 
proposed to amend the biologics regulations by removing the general 
safety test requirements for biological products. The document 
published with the incorrect title. This document corrects that error.

FOR FURTHER INFORMATION CONTACT: Lori J. Churchyard, Center for 
Biologics Evaluation and Research, Food and Drug Administration, 10903 
New Hampshire Ave., Bldg. 71, Rm. 7301, Silver Spring, MD 20993-0002, 
240-402-7911.

SUPPLEMENTARY INFORMATION: In the Federal Register of August 22, 2014, 
in FR Doc. 2014-19888, on page 49727, the following correction is made:
    1. On page 49727, in the third column, in the heading of the 
document, ``Revocation of General Safety Test Regulations That Are 
Duplicative of Requirements in Biological License Applications'' is 
corrected to read ``Revocation of General Safety Test Regulations That 
Are Duplicative of Requirements in Biologics License Applications''.

    Dated: September 3, 2014.
Leslie Kux,
Assistant Commissioner for Policy.
[FR Doc. 2014-21481 Filed 9-9-14; 8:45 am]
BILLING CODE 4164-01-P


