National Institutes of Health Training Grants, 42295-42296 [E6-11924]
Download as PDF
<![CDATA[
Federal Register / Vol. 71, No. 143 / Wednesday, July 26, 2006 / Rules and Regulations
rwilkins on PROD1PC63 with RULES_1
by State and local officials in the
development of regulatory policies that
have federalism implications.’’ ‘‘Policies
that have federalism implications’’ is
defined in the Executive order to
include regulations that have
‘‘substantial direct effects on the States,
on the relationship between the national
government and the States, or on the
distribution of power and
responsibilities among the various
levels of government.’’ This final rule
directly regulates growers, food
processors, food handlers and food
retailers, not States. This action does not
alter the relationships or distribution of
power and responsibilities established
by Congress in the preemption
provisions of section 408(n)(4) of the
FFDCA. For these same reasons, the
Agency has determined that this rule
does not have any ‘‘tribal implications’’
as described in Executive Order 13175,
entitled Consultation and Coordination
with Indian Tribal Governments (65 FR
67249, November 6, 2000). Executive
Order 13175, requires EPA to develop
an accountable process to ensure
‘‘meaningful and timely input by tribal
officials in the development of
regulatory policies that have tribal
implications.’’ ‘‘Policies that have tribal
implications’’ is defined in the
Executive order to include regulations
that have ‘‘substantial direct effects on
one or more Indian tribes, on the
relationship between the Federal
Government and the Indian tribes, or on
the distribution of power and
responsibilities between the Federal
Government and Indian tribes.’’ This
rule will not have substantial direct
effects on tribal governments, on the
relationship between the Federal
Government and Indian tribes, or on the
distribution of power and
responsibilities between the Federal
Government and Indian tribes, as
specified in Executive Order 13175.
Thus, Executive Order 13175 does not
apply to this rule.
XII. Congressional Review Act
The Congressional Review Act, 5
U.S.C. 801 et seq., as added by the Small
Business Regulatory Enforcement
Fairness Act of 1996, generally provides
that before a rule may take effect, the
agency promulgating the rule must
submit a rule report, which includes a
copy of the rule, to each House of the
Congress and to the Comptroller General
of the United States. EPA will submit a
report containing this rule and other
required information to the U.S. Senate,
the U.S. House of Representatives, and
the Comptroller General of the United
States prior to publication of this rule in
the Federal Register. This rule is not a
VerDate Aug<31>2005
16:29 Jul 25, 2006
Jkt 208001
‘‘major rule’’ as defined by 5 U.S.C.
804(2).
List of Subjects in 40 CFR Part 180
Environmental protection,
Administrative practice and procedure,
Agricultural commodities, Pesticides
and pests, Reporting and recordkeeping
requirements.
Dated: July 10, 2006.
Lois Rossi,
Director, Registration Division, Office of
Pesticide Programs.
Therefore, 40 CFR chapter I is
amended as follows:
I
PART 180—AMENDED
1. The authority citation for part 180
continues to read as follows:
I
Authority: 21 U.S.C. 321(q), 346a and 371.
2. Section 180.960 is amended by
adding alphabetically to the table a
polymer to read as follows:
I
§ 180.960 Polymers; exemptions from the
requirement of a tolerance.
*
*
*
*
*
Polymer
*
*
*
CAS No.
*
2-Propenoic Acid, 2-Methyl-,
Polymer with
Ethenylbenzene, 2-Ethylhexyl
2-Propenoate, 2-Hydroxyethyl
2-Propenoate, N(Hydroxymethyl) -2-Methyl-2Propenamide and Methyl 2Methyl-2-Propenoate, Ammonium Salt
*
*
*
*
*
146753–99–
3
*
[FR Doc. E6–11951 Filed 7–25–06; 8:45 am]
BILLING CODE 6560–50–S
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
42 CFR Part 63a
RIN 0925–AA28
National Institutes of Health Training
Grants
National Institutes of Health,
Department of Health and Human
Services.
ACTION: Final rule.
AGENCY:
SUMMARY: The National Institutes of
Health (NIH) is amending the current
regulations governing its training grants
to reflect applicability of the regulations
to institutional training grants
supporting pediatric research training.
PO 00000
Frm 00055
Fmt 4700
Sfmt 4700
42295
Effective Date: This final rule is
effective August 25, 2006.
FOR FURTHER INFORMATION CONTACT: Jerry
Moore, NIH Regulations Officer, Office
of Management Assessment, National
Institutes of Health, 6011 Executive
Boulevard, Suite 601, MSC 7669,
Rockville, Maryland 20892, telephone
301–496–4607 (not a toll-free number).
SUPPLEMENTARY INFORMATION: On
October 17, 2000, Congress enacted the
Children’s Health Act of 2000, Public
Law 106–310. Title X, section 1002, of
this law amended the Public Health
Service (PHS) Act by adding section
452G (42 U.S.C. 285g–10). Section 452G
directs the Director of the National
Institute of Child Health and Human
Development, after consultation with
the Administrator of the Health
Resources and Services Administration,
to support activities to provide for an
increase in the number and size of
institutional training grants to
institutions supporting pediatric
training. We are amending the current
regulations codified at 42 CFR part 63a,
‘‘National Institutes of Health Training
Grants,’’ to implement this pediatric
research training grants authority. More
specifically, we are amending part 63a
to reference section 452G of the PHS Act
in the authority section and in
paragraph (a)(2) of § 63a.1 of the
regulations, and update information in
the 18th, 19th, and 20th undesignated
paragraphs of § 63a.11.
We announced our intention to
amend the training grants regulations by
publishing the notice of proposed
rulemaking (NPRM), ‘‘National
Institutes of Health Training Grants,’’ in
the Federal Register of January 28, 2005
(70 FR 4080–4081). The NPRM provided
for a 60-day public comment period.
The comment period expired on March
29, 2005. We received no comments.
Therefore, the amending action reflected
in this final rule is the same as what we
proposed in the NPRM.
We provide the following as public
information.
DATES:
Executive Order 12866
Executive Order 12866, Regulatory
Planning and Review, requires that all
regulatory actions reflect consideration
of the costs and benefits they generate,
and that they meet certain standards,
such as avoiding the imposition of
unnecessary burdens on the affected
public. If a regulatory action is deemed
to fall within the scope of the definition
of the term ‘‘significant regulatory
action’’ contained in section 3(f) of the
Order, prepublication review by the
Office of Management and Budget’s
Office of Information and Regulatory
E:\FR\FM\26JYR1.SGM
26JYR1
42296
Federal Register / Vol. 71, No. 143 / Wednesday, July 26, 2006 / Rules and Regulations
Affairs (OIRA) is necessary. The OIRA
reviewed this final rule under Executive
Order 12866 and deemed it not a
significant regulatory action as defined
by the Executive Order.
Regulatory Flexibility Act
The Regulatory Flexibility Act (5
U.S.C. chapter 6) requires that
regulatory proposals be analyzed to
determine whether they create a
significant impact on a substantial
number of small entities. The Secretary
of Health and Human Services
(Secretary) certifies that this final rule
does not have such impact.
Executive Order 13132
Executive Order 13132, Federalism,
requires that Federal agencies consult
with State and local government
officials in the development of
regulatory policies with federalism
implications. The Secretary reviewed
this final rule as required under the
Executive Order and determined that it
does not have federalism implications.
The Secretary certifies that this final
rule will not have an effect on the
States, or on the distribution of power
and responsibilities among the various
levels of government.
Paperwork Reduction Act
This final rule does not contain
information collection requirements
which are subject to Office of
Management and Budget (OMB)
approval under the Paperwork
Reduction Act of 1995, as amended (44
U.S.C. chapter 35).
Catalogue of Federal Domestic
Assistance
The Catalogue of Federal Domestic
Assistance numbered program affected
by the proposed regulation is: 93.865.
List of Subjects in 42 CFR Part 63a
Grant programs—health; Health—
medical research.
FEDERAL COMMUNICATIONS
COMMISSION
2. Section 63a.1 is amended by
revising paragraph (a)(2) to read as
follows:
47 CFR Part 1
§ 63a.1 To what programs do these
regulations apply?
Payphone Line Rates; New Services
Test
(a) * * *
(2) Grants awarded by NIH for
research training with respect to the
human diseases, disorders, or other
aspects of human health or biomedical
research for which the institute or other
awarding component was established,
for which fellowship support is not
provided under section 487 of the Act
and which is not residency training of
physicians or other health professionals,
as authorized by sections 405(b)(1)(C),
452G, 485B(b), 2315(a)(1), and
2354(a)(3)(C) of the Act; and,
*
*
*
*
*
I 3. Section 63a.11 is amended by
revising the 18th, 19th, and 20th
undesignated paragraphs to read as
follows:
AGENCY:
I
§ 63a.11 Other HHS regulations and
policies that apply.
*
*
*
*
*
‘‘NIH Grants Policy Statement,’’
(December 1, 2003). This version is
located on the NIH Web site at: https://
grants./policy/nihgps_2003/index.htm.
[Note: this policy is subject to change, and
interested persons should contact the Office
of Policy for Extramural Research
Administration (OPERA), Office of
Extramural Research, NIH, 6701 Rockledge
Drive, Suite 350, MSC 7974, Bethesda,
Maryland 20892–7974, telephone 301–435–
0938 (or toll-free 800–518–4726), to obtain
references to the current version and any
amendments. Information may also be
obtained by contacting the OPERA Division
of Grants Policy via e-mail at https://
GrantsPolicy@mail.nih.gov. Previous
versions of the NIH Grants Policy Statement
are archived at https://grants.nih.gov/
grantspolicy/policy.htm.]
‘‘Public Health Service Policy on
Humane Care and Use of Laboratory
Animals,’’ Office of Laboratory Animal
Welfare (Amended August, 2002).
Dated: April 12, 2006.
Elias A. Zerhouni,
Director, National Institutes of Health.
PART 63a—NATIONAL INSTITUTES OF
HEALTH TRAINING GRANTS
[Note: this policy is subject to change, and
interested persons should contact the Office
of Laboratory Animal Welfare, 6705
Rockledge Drive, Suite 360, MSC 7982,
Bethesda, Maryland 20892–7982, telephone
301–594–2382 (not a toll-free number), to
obtain references to the current version and
any amendments. Information may also be
obtained by browsing the Office of
Laboratory Animal Welfare Home Page site
on the World Wide Web (https://
www.grants.nih.gov/grants/olaw/olaw.htm).]
1. The authority citation of part 63a is
revised to read as follows:
BILLING CODE 4140–01–P
Approved: July 18, 2006.
Michael O. Leavitt,
Secretary.
For the reasons set forth in the
preamble, we amend chapter 1 of title
42 of the Code of Federal Regulations as
set forth below.
I
rwilkins on PROD1PC63 with RULES_1
Authority: 42 U.S.C. 216, 2421(b)(3),
284(b)(1)(C), 285g–10, 287c(b), 300cc–
15(a)(1), 300cc–41(a)(3)(C), 7403(h)(2).
I
VerDate Aug<31>2005
17:27 Jul 25, 2006
Jkt 208001
[FR Doc. E6–11924 Filed 7–25–06; 8:45 am]
PO 00000
Frm 00056
Fmt 4700
Sfmt 4700
[File No. CCB/CPD No. 00–1; FCC 06–98]
Federal Communications
Commission.
ACTION: Final rule.
SUMMARY: The Commission issued this
document responding to a petition for
correction submitted by Verizon, Inc.
and a petition for reconsideration
submitted by the Wisconsin Pay
Telephone Association (WPTA). The
Commission granted Verizon’s petition
to correct the order by clarifying that
Verizon’s affiliate, Verizon North, is not
a Bell Operating Company (BOC) by
definition of the Act. The Commission
denied the WPTA’s petition for
reconsideration of the Commission’s
decision that the Wisconsin Public
Utility Commission should properly
determine BOC intrastate payphone line
rates in the State of Wisconsin to
determine compliance with the new
services test established by the
Commission.
DATES: Effective August 25, 2006.
FOR FURTHER INFORMATION CONTACT: Ana
Janckson-Curtis, Wireline Competition
Bureau, Pricing Policy Division, (202)
418–1530.
SUPPLEMENTARY INFORMATION: This is a
summary of the Commission’s order on
reconsideration in File No. CCB/CPD
No. 00–01 released on July 7, 2006. The
full text of this document is available on
the Commission’s Web site and for
public inspection during regular
business hours in the FCC Reference
Center, Room CY–A257, 445 Twelfth
Street, SW., Washington, DC 20554.
Procedural Matters
Paperwork Reduction Act Analysis
This document does not contain new
or modified information collection
requirements subject to the Paperwork
Reduction Act of 1995 (PRA), Public
Law 104–13. In addition, therefore, it
does not contain any new or modified
‘‘information collection burden for
small business concerns with fewer than
25 employees,’’ pursuant to the Small
Business Paperwork Relief Act of 2002,
Public Law 107–198, 44 U.S.C.
3506(c)(4).
Report to Congress
The Commission will not send a copy
of this order on reconsideration
pursuant to the Congressional Review
E:\FR\FM\26JYR1.SGM
26JYR1
]]>Agencies
[Federal Register Volume 71, Number 143 (Wednesday, July 26, 2006)]
[Rules and Regulations]
[Pages 42295-42296]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E6-11924]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
42 CFR Part 63a
RIN 0925-AA28
National Institutes of Health Training Grants
AGENCY: National Institutes of Health, Department of Health and Human
Services.
ACTION: Final rule.
-----------------------------------------------------------------------
SUMMARY: The National Institutes of Health (NIH) is amending the
current regulations governing its training grants to reflect
applicability of the regulations to institutional training grants
supporting pediatric research training.
DATES: Effective Date: This final rule is effective August 25, 2006.
FOR FURTHER INFORMATION CONTACT: Jerry Moore, NIH Regulations Officer,
Office of Management Assessment, National Institutes of Health, 6011
Executive Boulevard, Suite 601, MSC 7669, Rockville, Maryland 20892,
telephone 301-496-4607 (not a toll-free number).
SUPPLEMENTARY INFORMATION: On October 17, 2000, Congress enacted the
Children's Health Act of 2000, Public Law 106-310. Title X, section
1002, of this law amended the Public Health Service (PHS) Act by adding
section 452G (42 U.S.C. 285g-10). Section 452G directs the Director of
the National Institute of Child Health and Human Development, after
consultation with the Administrator of the Health Resources and
Services Administration, to support activities to provide for an
increase in the number and size of institutional training grants to
institutions supporting pediatric training. We are amending the current
regulations codified at 42 CFR part 63a, ``National Institutes of
Health Training Grants,'' to implement this pediatric research training
grants authority. More specifically, we are amending part 63a to
reference section 452G of the PHS Act in the authority section and in
paragraph (a)(2) of Sec. 63a.1 of the regulations, and update
information in the 18th, 19th, and 20th undesignated paragraphs of
Sec. 63a.11.
We announced our intention to amend the training grants regulations
by publishing the notice of proposed rulemaking (NPRM), ``National
Institutes of Health Training Grants,'' in the Federal Register of
January 28, 2005 (70 FR 4080-4081). The NPRM provided for a 60-day
public comment period. The comment period expired on March 29, 2005. We
received no comments. Therefore, the amending action reflected in this
final rule is the same as what we proposed in the NPRM.
We provide the following as public information.
Executive Order 12866
Executive Order 12866, Regulatory Planning and Review, requires
that all regulatory actions reflect consideration of the costs and
benefits they generate, and that they meet certain standards, such as
avoiding the imposition of unnecessary burdens on the affected public.
If a regulatory action is deemed to fall within the scope of the
definition of the term ``significant regulatory action'' contained in
section 3(f) of the Order, prepublication review by the Office of
Management and Budget's Office of Information and Regulatory
[[Page 42296]]
Affairs (OIRA) is necessary. The OIRA reviewed this final rule under
Executive Order 12866 and deemed it not a significant regulatory action
as defined by the Executive Order.
Regulatory Flexibility Act
The Regulatory Flexibility Act (5 U.S.C. chapter 6) requires that
regulatory proposals be analyzed to determine whether they create a
significant impact on a substantial number of small entities. The
Secretary of Health and Human Services (Secretary) certifies that this
final rule does not have such impact.
Executive Order 13132
Executive Order 13132, Federalism, requires that Federal agencies
consult with State and local government officials in the development of
regulatory policies with federalism implications. The Secretary
reviewed this final rule as required under the Executive Order and
determined that it does not have federalism implications. The Secretary
certifies that this final rule will not have an effect on the States,
or on the distribution of power and responsibilities among the various
levels of government.
Paperwork Reduction Act
This final rule does not contain information collection
requirements which are subject to Office of Management and Budget (OMB)
approval under the Paperwork Reduction Act of 1995, as amended (44
U.S.C. chapter 35).
Catalogue of Federal Domestic Assistance
The Catalogue of Federal Domestic Assistance numbered program
affected by the proposed regulation is: 93.865.
List of Subjects in 42 CFR Part 63a
Grant programs--health; Health--medical research.
Dated: April 12, 2006.
Elias A. Zerhouni,
Director, National Institutes of Health.
Approved: July 18, 2006.
Michael O. Leavitt,
Secretary.
0
For the reasons set forth in the preamble, we amend chapter 1 of title
42 of the Code of Federal Regulations as set forth below.
PART 63a--NATIONAL INSTITUTES OF HEALTH TRAINING GRANTS
0
1. The authority citation of part 63a is revised to read as follows:
Authority: 42 U.S.C. 216, 2421(b)(3), 284(b)(1)(C), 285g-10,
287c(b), 300cc-15(a)(1), 300cc-41(a)(3)(C), 7403(h)(2).
0
2. Section 63a.1 is amended by revising paragraph (a)(2) to read as
follows:
Sec. 63a.1 To what programs do these regulations apply?
(a) * * *
(2) Grants awarded by NIH for research training with respect to the
human diseases, disorders, or other aspects of human health or
biomedical research for which the institute or other awarding component
was established, for which fellowship support is not provided under
section 487 of the Act and which is not residency training of
physicians or other health professionals, as authorized by sections
405(b)(1)(C), 452G, 485B(b), 2315(a)(1), and 2354(a)(3)(C) of the Act;
and,
* * * * *
0
3. Section 63a.11 is amended by revising the 18th, 19th, and 20th
undesignated paragraphs to read as follows:
Sec. 63a.11 Other HHS regulations and policies that apply.
* * * * *
``NIH Grants Policy Statement,'' (December 1, 2003). This version
is located on the NIH Web site at: https://grants./policy/nihgps--2003/
index.htm.
[Note:
this policy is subject to change, and interested persons should
contact the Office of Policy for Extramural Research Administration
(OPERA), Office of Extramural Research, NIH, 6701 Rockledge Drive,
Suite 350, MSC 7974, Bethesda, Maryland 20892-7974, telephone 301-
435-0938 (or toll-free 800-518-4726), to obtain references to the
current version and any amendments. Information may also be obtained
by contacting the OPERA Division of Grants Policy via e-mail at
https://GrantsPolicy@mail.nih.gov. Previous versions of the NIH
Grants Policy Statement are archived at https://grants.nih.gov/
grantspolicy/policy.htm.]
``Public Health Service Policy on Humane Care and Use of Laboratory
Animals,'' Office of Laboratory Animal Welfare (Amended August, 2002).
[Note:
this policy is subject to change, and interested persons should
contact the Office of Laboratory Animal Welfare, 6705 Rockledge
Drive, Suite 360, MSC 7982, Bethesda, Maryland 20892-7982, telephone
301-594-2382 (not a toll-free number), to obtain references to the
current version and any amendments. Information may also be obtained
by browsing the Office of Laboratory Animal Welfare Home Page site
on the World Wide Web (https://www.grants.nih.gov/grants/olaw/
olaw.htm).]
[FR Doc. E6-11924 Filed 7-25-06; 8:45 am]
BILLING CODE 4140-01-P
