Proposed Rules. Proposed rule; correction
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/register/2014/09/10/2014-21481A research copy — for the controlling text, always check the official state or federal source. Not legal advice.
BILLING CODE 4910-13-P 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. 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]