Agency Information Collection Activities; Proposed Collection; Comment Request; Small Business Innovation Research Program-Phase II, 66538-66539 [2015-27512]
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Federal Register / Vol. 80, No. 209 / Thursday, October 29, 2015 / Notices
Prevention and the Agency for Toxic
Substances and Disease Registry.
Catherine Ramadei,
Acting Director, Management Analysis and
Services Office, Centers for Disease Control
and Prevention.
[FR Doc. 2015–27563 Filed 10–28–15; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration on Community Living
Proposed Information Collection
Activity; Comment Request; State
Developmental Disabilities Council—
Annual Program Performance Report
(PPR)
Administration on Intellectual
and Developmental Disabilities,
Administration for Community Living,
HHS.
ACTION: Notice.
AGENCY:
A Plan developed by the State
Council on Developmental Disabilities
is required by federal statute. Each State
Council on Developmental Disabilities
must develop the plan, provide for
public comments in the State, provide
for approval by the State’s Governor,
and finally submit the plan on a five-
SUMMARY:
year basis. On an annual basis, the
Council must submit a Program
Performance Report (PPR) to described
the extent to which annual progress is
being achieved on the 5 year state plan
goals. The PPR will be used by (1) the
Council as a planning document to track
progress made in meeting state plan
goals; (2) the citizenry of the State as a
mechanism for monitoring progress and
activities on the plans of the Council; (4)
the Department as a stewardship tool,
for ensuring compliance with the
Developmental Disabilities Assistance
and Bill of Rights Act, as one basis for
monitoring and providing technical
assistance (e.g., during site visits), and
as a support for management decision
making.
Submit written comments on the
collection of information by November
30, 2015.
ADDRESSES: Submit written comments
on the collection of information by fax
202.395.5806 or by email to OIRA_
submission@omb.eop.gov, Attn: OMB
Desk Officer for ACL.
FOR FURTHER INFORMATION CONTACT:
Allison Cruz, Administration on
Community Living, Administration on
Intellectual and Developmental
Disabilities, Office of Program Support,
One Massachusetts Avenue NW., Room
DATES:
4306, Washington, DC 20201, 202–357–
3439.
In
compliance with the requirements of
Section 506 (c)(2)(A) of the Paperwork
Reduction Act of 1995, the
Administration on Community Living is
soliciting public comment on the
specific aspects of the information
collection described above. The
Department specifically requests
comments on: (a) Whether the proposed
Collection of information is necessary
for the proper performance of the
function of the agency, including
whether the information shall have
practical utility; (b) the accuracy of the
agency’s estimate of the burden of the
proposed collection of information; (c)
the quality, utility, and clarity of the
information to be collected; (d) ways to
minimize the burden information to be
collected; and (e) ways to minimize the
burden of the collection of information
on respondents, including through the
use of automated collection technique
comments and or other forms of
information technology. Consideration
will be given to comments and
suggestions submitted within 30 days of
this publication.
Respondents: 56 State Developmental
Disabilities Councils.
SUPPLEMENTARY INFORMATION:
ANNUAL BURDEN ESTIMATES
Number of
respondents
Instrument
State Developmental Disabilities Program Performance Report (PPR) .........
Estimated Total Annual Burden
Hours: 7728.
ACTION:
Dated: October 23, 2015.
Kathy Greenlee,
Administrator and Assistant Secretary for
Aging.
SUMMARY:
[FR Doc. 2015–27511 Filed 10–28–15; 8:45 am]
BILLING CODE 4154–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
asabaliauskas on DSK5VPTVN1PROD with NOTICES
Administration for Community Living
Agency Information Collection
Activities; Proposed Collection;
Comment Request; Small Business
Innovation Research Program—Phase
II
National Institute on Disability,
Independent Living and Rehabilitation,
Administration for Community Living
(ACL), HHS.
AGENCY:
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1
Average
burden hours
per response
Total burden
hours
138
7728
Submit comments on the
collection of information by November
30, 2015.
DATES:
The Administration for
Community Living (ACL), National
Institute on Disability, Independent
Living, and Rehabilitation Research
(NIDLRR) is announcing that the
proposed collection of information
listed below has been submitted to the
Office of Management and Budget
(OMB) for review and clearance under
the Paperwork Reduction Act of 1995.
This notice solicits comments on the
information collection requirements
relating to the Small Business
Innovation Research Program (SBIR)—
Phase II. Specifically, the information
collection is the SBIR Application
package, which provides information on
requirements for the application
including mandatory information
provided via government- approved
forms.
PO 00000
Number of
responses per
respondent
Sfmt 4703
Submit comments on the
collection of information by fax
202.395.5806 or by email to OIRA_
submission@omb.eop.gov, Attn: OMB
Desk Officer for ACL.
ADDRESSES:
FOR FURTHER INFORMATION CONTACT:
Brian Bard 202–254–7345 or
Brian.Bard@acl.hhs.gov.
Under the
PRA (44 U.S.C. 3501–3520), Federal
agencies must obtain approval from the
Office of Management and Budget
(OMB) for each collection of
information they conduct or sponsor.
‘‘Collection of information’’ is defined
in 44 U.S.C. 3502(3) and 5 CFR
1320.3(c) and includes agency request
or requirements that members of the
public submit reports, keep records, or
provide information to a third party.
Section 3506(c)(2)(A) of the PRA (44
SUPPLEMENTARY INFORMATION:
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Federal Register / Vol. 80, No. 209 / Thursday, October 29, 2015 / Notices
U.S.C. 3506(c)(2)(A)) requires Federal
agencies to provide a 60-day notice in
the Federal Register concerning each
proposed collection of information,
including each proposed extension of an
existing collection of information,
before submitting the collection to OMB
for approval. This information
collection is the SBIR Application
Package. To comply with this
requirement, ACL/NIDILRR published a
notice of the proposed collection of
information set forth in this document,
inviting comment on: (1) Whether the
proposed collection of information is
necessary for the proper performance of
ACL/NIDILRR’s functions, including
whether the information will have
practical utility; (2) the accuracy of
ACL/NIDILRR’s estimate of the burden
of the proposed collection of
information, including the validity of
the methodology and assumptions used;
(3) ways to enhance the quality, utility,
and clarity of the information to be
collected; and (4) ways to minimize the
burden of the collection of information
on respondents, including through the
use of automated collection techniques
when appropriate, and other forms of
information technology. NIDILRR
received one comment asking for more
information on the method by which it
calculated burden. The Application
Package, including instructions and
forms, has been in continuous use with
minor modifications since it was first
approved by OMB in FY2012. This
request is for approval to extent the
current form and instructions, with
minor modifications to change the
sponsoring agency from Department of
Education to Department of Health and
Human Services (per requirement of the
Workforce Innovation Opportunity Act)
for three years, covering the FY 2015–
2017 reporting periods.
Dated: October 23, 2015.
Kathy Greenlee,
Administrator and Assistant Secretary for
Aging.
[FR Doc. 2015–27512 Filed 10–28–15; 8:45 am]
asabaliauskas on DSK5VPTVN1PROD with NOTICES
BILLING CODE 4154–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2009–D–0268]
Agency Information Collection
Activities; Submission for Office of
Management and Budget Review;
Comment Request; Labeling of Certain
Beers Subject to the Labeling
Jurisdiction of the Food and Drug
Administration
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice of availability.
The Food and Drug
Administration (FDA) is announcing
that a proposed collection of
information has been submitted to the
Office of Management and Budget
(OMB) for review and clearance under
the Paperwork Reduction Act of 1995.
DATES: Fax written comments on the
collection of information by November
30, 2015.
ADDRESSES: You may submit comments
as follows:
SUMMARY:
Electronic Submissions
Submit electronic comments in the
following way:
• Federal eRulemaking Portal: https://
www.regulations.gov. Follow the
instructions for submitting comments.
Comments submitted electronically,
including attachments, to https://
www.regulations.gov will be posted to
the docket unchanged. Because your
comment will be made public, you are
solely responsible for ensuring that your
comment does not include any
confidential information that you or a
third party may not wish to be posted,
such as medical information, your or
anyone else’s Social Security number, or
confidential business information, such
as a manufacturing process. Please note
that if you include your name, contact
information, or other information that
identifies you in the body of your
comments, that information will be
posted on https://www.regulations.gov.
• If you want to submit a comment
with confidential information that you
do not wish to be made available to the
public, submit the comment as a
written/paper submission and in the
manner detailed (see ‘‘Written/Paper
Submissions’’ and ‘‘Instructions’’).
Written/Paper Submissions
Submit written/paper submissions as
follows:
• Mail/Hand delivery/Courier (for
written/paper submissions): Division of
Dockets Management (HFA–305), Food
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66539
and Drug Administration, 5630 Fishers
Lane, Rm. 1061, Rockville, MD 20852.
• For written/paper comments
submitted to the Division of Dockets
Management, FDA will post your
comment, as well as any attachments,
except for information submitted,
marked and identified, as confidential,
if submitted as detailed in
‘‘Instructions.’’
Instructions: All submissions received
must include the Docket No. FDA–
2009–D–0268. Received comments will
be placed in the docket and, except for
those submitted as ‘‘Confidential
Submissions,’’ publicly viewable at
https://www.regulations.gov or at the
Division of Dockets Management
between 9 a.m. and 4 p.m., Monday
through Friday.
• Confidential Submissions—To
submit a comment with confidential
information that you do not wish to be
made publicly available, submit your
comments only as a written/paper
submission. You should submit two
copies total. One copy will include the
information you claim to be confidential
with a heading or cover note that states
‘‘THIS DOCUMENT CONTAINS
CONFIDENTIAL INFORMATION.’’ The
Agency will review this copy, including
the claimed confidential information, in
its consideration of comments. The
second copy, which will have the
claimed confidential information
redacted/blacked out, will be available
for public viewing and posted on
https://www.regulations.gov. Submit
both copies to the Division of Dockets
Management. If you do not wish your
name and contact information to be
made publicly available, you can
provide this information on the cover
sheet and not in the body of your
comments and you must identify this
information as ‘‘confidential.’’ Any
information marked as ‘‘confidential’’
will not be disclosed except in
accordance with 21 CFR 10.20 and other
applicable disclosure law. For more
information about FDA’s posting of
comments to public dockets, see 80 FR
56469, September 18, 2015, or access
the information at: https://www.fda.gov/
regulatoryinformation/dockets/
default.htm.
Docket: For access to the docket to
read background documents or the
electronic and written/paper comments
received, go to https://
www.regulations.gov and insert the
docket number, found in brackets in the
heading of this document, into the
‘‘Search’’ box and follow the prompts
and/or go to the Division of Dockets
Management, 5630 Fishers Lane, rm.
1061, Rockville, MD 20852.
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]]>Agencies
[Federal Register Volume 80, Number 209 (Thursday, October 29, 2015)]
[Notices]
[Pages 66538-66539]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2015-27512]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Community Living
Agency Information Collection Activities; Proposed Collection;
Comment Request; Small Business Innovation Research Program--Phase II
AGENCY: National Institute on Disability, Independent Living and
Rehabilitation, Administration for Community Living (ACL), HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Administration for Community Living (ACL), National
Institute on Disability, Independent Living, and Rehabilitation
Research (NIDLRR) is announcing that the proposed collection of
information listed below has been submitted to the Office of Management
and Budget (OMB) for review and clearance under the Paperwork Reduction
Act of 1995. This notice solicits comments on the information
collection requirements relating to the Small Business Innovation
Research Program (SBIR)--Phase II. Specifically, the information
collection is the SBIR Application package, which provides information
on requirements for the application including mandatory information
provided via government- approved forms.
DATES: Submit comments on the collection of information by November 30,
2015.
ADDRESSES: Submit comments on the collection of information by fax
202.395.5806 or by email to OIRA_submission@omb.eop.gov, Attn: OMB Desk
Officer for ACL.
FOR FURTHER INFORMATION CONTACT: Brian Bard 202-254-7345 or
Brian.Bard@acl.hhs.gov.
SUPPLEMENTARY INFORMATION: Under the PRA (44 U.S.C. 3501-3520), Federal
agencies must obtain approval from the Office of Management and Budget
(OMB) for each collection of information they conduct or sponsor.
``Collection of information'' is defined in 44 U.S.C. 3502(3) and 5 CFR
1320.3(c) and includes agency request or requirements that members of
the public submit reports, keep records, or provide information to a
third party. Section 3506(c)(2)(A) of the PRA (44
[[Page 66539]]
U.S.C. 3506(c)(2)(A)) requires Federal agencies to provide a 60-day
notice in the Federal Register concerning each proposed collection of
information, including each proposed extension of an existing
collection of information, before submitting the collection to OMB for
approval. This information collection is the SBIR Application Package.
To comply with this requirement, ACL/NIDILRR published a notice of the
proposed collection of information set forth in this document, inviting
comment on: (1) Whether the proposed collection of information is
necessary for the proper performance of ACL/NIDILRR's functions,
including whether the information will have practical utility; (2) the
accuracy of ACL/NIDILRR's estimate of the burden of the proposed
collection of information, including the validity of the methodology
and assumptions used; (3) ways to enhance the quality, utility, and
clarity of the information to be collected; and (4) ways to minimize
the burden of the collection of information on respondents, including
through the use of automated collection techniques when appropriate,
and other forms of information technology. NIDILRR received one comment
asking for more information on the method by which it calculated
burden. The Application Package, including instructions and forms, has
been in continuous use with minor modifications since it was first
approved by OMB in FY2012. This request is for approval to extent the
current form and instructions, with minor modifications to change the
sponsoring agency from Department of Education to Department of Health
and Human Services (per requirement of the Workforce Innovation
Opportunity Act) for three years, covering the FY 2015-2017 reporting
periods.
Dated: October 23, 2015.
Kathy Greenlee,
Administrator and Assistant Secretary for Aging.
[FR Doc. 2015-27512 Filed 10-28-15; 8:45 am]
BILLING CODE 4154-01-P
