Viruses, Serums, Toxins, and Analogous Products; Single Label Claim for Veterinary Biological Products, 47005 [2016-17073]
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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 https://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 ‘‘(https://
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
https://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.
-----------------------------------------------------------------------
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.
---------------------------------------------------------------------------
\1\ To view the final rule and supporting documents, go to
https://www.regulations.gov/#!docketDetail;D=APHIS-2011-0049.
---------------------------------------------------------------------------
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 ``(https://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
