Viruses, Serums, Toxins, and Analogous Products; Single Label Claim for Veterinary Biological Products, 47005 [2016-17073]

Download as PDF Federal Register / Vol. 81, No. 139 / Wednesday, July 20, 2016 / Rules and Regulations Lists of Subjects in 9 CFR Part 112 DEPARTMENT OF AGRICULTURE Animal biologics, Exports, Imports, Labeling, packaging and containers, Reporting and recordkeeping requirements. Accordingly, we are amending 9 CFR part 112 as follows: Animal and Plant Health Inspection Service 9 CFR Part 112 [Docket No. APHIS–2011–0049] PART 112—PACKAGING AND LABELING RIN 0579–AD64 1. The authority citation for part 112 continues to read as follows: Viruses, Serums, Toxins, and Analogous Products; Single Label Claim for Veterinary Biological Products ■ Animal and Plant Health Inspection Service, USDA. ACTION: Final rule; technical amendment. § 112.5 Authority: 21 U.S.C. 151–159; 7 CFR 2.22, 2.80, and 371.4. AGENCY: In a final rule published in the Federal Register on July 10, 2015, and effective on September 8, 2015, we amended the Virus-Serum-Toxin Act regulations to provide for the use of a simpler labeling format that would better communicate product performance to the user. Among other things, we provided the address of a Web site for accessing transmittal forms to be used with each submission of sketches and labels. However, the Web site address provided is incorrect. Therefore, we are amending the regulations to provide the correct address. SUMMARY: DATES: Effective July 20, 2016. rmajette on DSK2TPTVN1PROD with RULES FOR FURTHER INFORMATION CONTACT: VerDate Sep<11>2014 14:53 Jul 19, 2016 Jkt 238001 Done in Washington, DC, this 14th day of July 2016. Jere L. Dick, Acting Administrator, Animal and Plant Health Inspection Service. [FR Doc. 2016–17073 Filed 7–19–16; 8:45 am] BILLING CODE 3410–34–P NUCLEAR REGULATORY COMMISSION 10 CFR Part 2 [NRC–2016–0117] Dr. Donna Malloy, Operational Support Section, Center for Veterinary Biologics, Policy, Evaluation, and Licensing, VS, APHIS, 4700 River Road, Unit 148, Riverdale, MD 20737; (301) 851–2352. SUPPLEMENTARY INFORMATION: In a final rule 1 that was published in the Federal Register on July 10, 2015 (80 FR 39669– 39675, Docket No. APHIS–2011–0049), and effective on September 8, 2015, we amended the Virus-Serum-Toxin Act regulations to provide for the use of a simpler labeling format that would better communicate product performance to the user. Among other things, we provided the address of a Web site in § 112.5(a) for accessing transmittal forms to be used with each submission of sketches (including proofs) and labels. However, the Web site address provided is for accessing product licensing data and not transmittal forms. Therefore, we are amending § 112.5(a) to correct the address. 1 To view the final rule and supporting documents, go to http://www.regulations.gov/ #!docketDetail;D=APHIS-2011-0049. [Amended] 2. In § 112.5, paragraph (a) is amended by removing the words ‘‘(productdata.aphis.usda.gov)’’ and adding the words ‘‘(http:// www.aphis.usda.gov/animalhealth/cvb/ forms)’’ in their place. ■ RIN 3150–AJ76 Update to Transcript Correction Procedures Nuclear Regulatory Commission. ACTION: Final rule. AGENCY: The U.S. Nuclear Regulatory Commission (NRC) is amending its regulation that governs the correction of official transcripts for agency adjudicatory proceedings. The current regulation has not been substantively updated since it was adopted in 1962 and the NRC’s internal procedures have evolved since that time to incorporate technological development. The NRC is not soliciting public comment on this change because the change is limited to an agency rule of procedure and practice that does not affect the rights and responsibilities of outside parties. DATES: This final rule is effective on July 20, 2016. ADDRESSES: Please refer to Docket ID NRC–2016–0117 when contacting the NRC about the availability of information for this action. You may SUMMARY: PO 00000 Frm 00005 Fmt 4700 Sfmt 4700 47005 obtain publicly-available information related to this action by any of the following methods: • Federal Rulemaking Web site: Go to http://www.regulations.gov and search for Docket ID NRC–2016–0117. Address questions about NRC dockets to Carol Gallagher; telephone: 301–415–3463; email: Carol.Gallagher@nrc.gov. For other questions, contact the individual listed in the FOR FURTHER INFORMATION CONTACT section of this document. • NRC’s Public Document Room (PDR): You may examine and purchase copies of public documents at the NRC’s PDR, Room O1–F21, One White Flint North, 11555 Rockville Pike, Rockville, Maryland 20852. FOR FURTHER INFORMATION CONTACT: Tison Campbell, Office of the General Counsel, telephone: 301–287–9290, email: Tison.Campbell@nrc.gov, U.S. Nuclear Regulatory Commission, Washington DC 20555–0001. SUPPLEMENTARY INFORMATION: I. Summary of Changes In 1962, the Atomic Energy Commission (the NRC’s predecessor agency) adopted revised rules of practice and procedure to govern the conduct of adjudicatory proceedings before the agency (27 FR 377; January 13, 1962). As part of those regulations, the Commission adopted a paragraph governing the correction of hearing transcripts. That provision, originally at § 2.750(b) of title 10 of the Code of Federal Regulations (10 CFR), provided specific, prescriptive direction to the Commission’s staff regarding the method for recording and showing corrections to transcripts. For example, the Secretary was directed to make any physical corrections to the official transcript, not by replacing pages, but by drawing a line through the text to be changed in the original transcript and writing the correct text immediately above. The current agency practice varies. In Commission proceedings, an appendix listing the transcript corrections and a clean version of the transcript are attached to the order adopting the parties’ proposed transcript corrections. In Atomic Safety and Licensing Board Panel proceedings, the boards generally issue an order adopting the parties’ joint proposed transcript corrections, with or without an appendix listing the corrections. The Secretary does not prepare transcripts of board proceedings. The NRC is, therefore, updating the regulation that governs the correction of official transcripts for agency adjudicatory proceedings, currently at E:\FR\FM\20JYR1.SGM 20JYR1

Agencies

[Federal Register Volume 81, Number 139 (Wednesday, July 20, 2016)]
[Rules and Regulations]
[Page 47005]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-17073]



[[Page 47005]]

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DEPARTMENT OF AGRICULTURE

Animal and Plant Health Inspection Service

9 CFR Part 112

[Docket No. APHIS-2011-0049]
RIN 0579-AD64


Viruses, Serums, Toxins, and Analogous Products; Single Label 
Claim for Veterinary Biological Products

AGENCY: Animal and Plant Health Inspection Service, USDA.

ACTION: Final rule; technical amendment.

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SUMMARY: In a final rule published in the Federal Register on July 10, 
2015, and effective on September 8, 2015, we amended the Virus-Serum-
Toxin Act regulations to provide for the use of a simpler labeling 
format that would better communicate product performance to the user. 
Among other things, we provided the address of a Web site for accessing 
transmittal forms to be used with each submission of sketches and 
labels. However, the Web site address provided is incorrect. Therefore, 
we are amending the regulations to provide the correct address.

DATES: Effective July 20, 2016.

FOR FURTHER INFORMATION CONTACT: Dr. Donna Malloy, Operational Support 
Section, Center for Veterinary Biologics, Policy, Evaluation, and 
Licensing, VS, APHIS, 4700 River Road, Unit 148, Riverdale, MD 20737; 
(301) 851-2352.

SUPPLEMENTARY INFORMATION: In a final rule \1\ that was published in 
the Federal Register on July 10, 2015 (80 FR 39669-39675, Docket No. 
APHIS-2011-0049), and effective on September 8, 2015, we amended the 
Virus-Serum-Toxin Act regulations to provide for the use of a simpler 
labeling format that would better communicate product performance to 
the user. Among other things, we provided the address of a Web site in 
Sec.  112.5(a) for accessing transmittal forms to be used with each 
submission of sketches (including proofs) and labels. However, the Web 
site address provided is for accessing product licensing data and not 
transmittal forms. Therefore, we are amending Sec.  112.5(a) to correct 
the address.
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    \1\ To view the final rule and supporting documents, go to 
http://www.regulations.gov/#!docketDetail;D=APHIS-2011-0049.
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Lists of Subjects in 9 CFR Part 112

    Animal biologics, Exports, Imports, Labeling, packaging and 
containers, Reporting and recordkeeping requirements.

    Accordingly, we are amending 9 CFR part 112 as follows:

PART 112--PACKAGING AND LABELING

0
1. The authority citation for part 112 continues to read as follows:

    Authority:  21 U.S.C. 151-159; 7 CFR 2.22, 2.80, and 371.4.


Sec.  112.5  [Amended]

0
2. In Sec.  112.5, paragraph (a) is amended by removing the words 
``(productdata.aphis.usda.gov)'' and adding the words ``(http://www.aphis.usda.gov/animalhealth/cvb/forms)'' in their place.

    Done in Washington, DC, this 14th day of July 2016.
Jere L. Dick,
Acting Administrator, Animal and Plant Health Inspection Service.
[FR Doc. 2016-17073 Filed 7-19-16; 8:45 am]
 BILLING CODE 3410-34-P