Submission for OMB Review; Comment Request, 17548-17549 [2014-06931]
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17548
Federal Register / Vol. 79, No. 60 / Friday, March 28, 2014 / Notices
ANNUAL BURDEN ESTIMATES—NEW INSTRUMENT
Instrument
Total
number of
respondents
Annual
number of
respondents
Number of
responses
per
respondent
Average
burden
hour per
response
Total
annual
burden
hours 1
Participant 30-month survey ................................................
11,840
3,947
1
.5
1,974
ANNUAL BURDEN ESTIMATES—CHANGES TO ESTIMATED NUMBER OF RESPONDENTS
[Instruments previously approved]
Previously approved instrument
Updates to total number
of respondents
Participant Contact Information Form (5 STED
sites).
Participant Baseline Information Form (5 STED
sites).
Participant STED tracking letters .........................
Updates to
annual
number
respondents
2800 additional respondents.
2800 additional respondents.
2178 additional respondents.
960 additional respondents.
960 fewer respondents
1440 additional respondents.
800 additional respondents.
Participant 6-month survey (Adult sites) ..............
Participant 6-month survey (Young Adult sites) ...
Participant 12-month survey (Adult sites) ............
Participant 12-month survey (Young Adult sites)
Number of
responses per
respondent
Average
burden
hour per
response
Updated
annual burden
hours 1
933
1
.08
75
933
1
.17
159
726
5
.05
182
320
1
.5
160
¥320
480
1
1
.5
.75
¥160
360
267
1
.75
200
mstockstill on DSK4VPTVN1PROD with NOTICES
Increase in Est. Annual Burden Hours for Previously Approved ICs: 976.
In compliance with the requirements
of Section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995, the
Administration for Children and
Families and the Employment and
Training Administration are soliciting
public comment on the specific aspects
of the information collection described
above. Copies of the proposed collection
of information can be obtained and
comments may be forwarded by writing
to the Administration for Children and
Families, Office of Planning, Research
and Evaluation, 370 L’Enfant
Promenade SW., Washington, DC 20447,
Attn: OPRE Reports Clearance Officer.
Email address: OPREinfocollection@
acf.hhs.gov. All requests should be
identified by the title of the information
collection.
The Department specifically requests
comments on (a) whether the proposed
collection of information is necessary
for the proper performance of the
functions of the agencies, including
whether the information shall have
practical utility; (b) the accuracy of the
agencies’ estimate of the burden of the
proposed collection of information; (c)
the quality, utility, and clarity of the
information to be collected; and (d)
ways to minimize the burden of the
collection of information on
respondents, including through the use
of automated collection techniques or
VerDate Mar<15>2010
18:57 Mar 27, 2014
Jkt 232001
other forms of information technology.
Consideration will be given to
comments and suggestions submitted
within 60 days of this publication.
Karl Koerper,
Reports Clearance Officer.
[FR Doc. 2014–06937 Filed 3–27–14; 8:45 am]
BILLING CODE 4184–09–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Submission for OMB Review;
Comment Request
Title: Request for Specific Consent to
Juvenile Court Jurisdiction.
OMB No.: 0970–0385.
Description: The William Wilberforce
Trafficking Victims Protection
Reauthorization Act of 2008 (TVPRA of
2008), Public Law 110–457 was enacted
into law December 23, 2008. Section
235(d) directs the Secretary of HHS to
grant or deny requests for specific
consent for unaccompanied alien
children in HHS custody who seek to
invoke the jurisdiction of a state court
for a dependency order and who also
seek to invoke the jurisdiction of a state
court to determine or alter his or her
PO 00000
Frm 00055
Fmt 4703
Sfmt 4703
custody status or release from ORR.
These requests can be extremely time
sensitive since a child must ask a state
court for dependency before turning 18
years old.
In developing procedures for
collecting the necessary information
from unaccompanied alien children,
their attorneys, or other representatives
to allow HHS to approve or deny
consent requests, ORR/DUCS devised a
form. Specifically, the form asks the
requestor for his/her identifying
information, basic identifying
information on the unaccompanied
alien child, the name of the HHS-funded
facility where the child is in HHS
custody and care, the name of the court
and its location, and the kind of request
(e.g., for a change in custody, etc.). The
form also asks that the unaccompanied
alien child’s attorney or authorized
representative attach a Notice of
Representation, which is an approved
federal government agency form used
for immigration procedures that
authorizes the attorney to act on behalf
of the child (i.e.,G–28, EOIR–28, EOIR–
29), or any other form of authorization
to act on behalf of the unaccompanied
alien child.
Respondents: Attorneys, accredited
legal representatives, or others
authorized to act on behalf of a
unaccompanied alien child.
E:\FR\FM\28MRN1.SGM
28MRN1
17549
Federal Register / Vol. 79, No. 60 / Friday, March 28, 2014 / Notices
ANNUAL BURDEN ESTIMATES
Instrument
Number of
respondents
Number of
responses per
respondent
Average
burden hours
per response
Total
burden hours
Request for Specific Consent ........................................................
30
1
0.33
9.9
Estimated Total Annual Burden
Hours: 9.9
Additional Information: Copies of the
proposed collection may be obtained by
writing to the Administration for
Children and Families, Office of
Planning, Research and Evaluation, 370
L’Enfant Promenade SW., Washington,
DC 20447, Attn: ACF Reports Clearance
Officer. All requests should be
identified by the title of the information
collection. Email address:
infocollection@acf.hhs.gov.
OMB Comment: OMB is required to
make a decision concerning the
collection of information between 30
and 60 days after publication of this
document in the Federal Register.
Therefore, a comment is best assured of
having its full effect if OMB receives it
within 30 days of publication. Written
comments and recommendations for the
proposed information collection should
be sent directly to the following: Office
of Management and Budget,, Paperwork
Reduction Project, Fax: 202–395–7285,
Email: OIRA_SUBMISSION@
OMB.EOP.GOV.
Attn: Desk Officer for the
Administration for Children and
Families.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 2014–06931 Filed 3–27–14; 8:45 am]
BILLING CODE 4184–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2013–N–0723]
mstockstill on DSK4VPTVN1PROD with NOTICES
Agency Information Collection
Activities; Submission for Office of
Management and Budget Review;
Comment Request; Reports of
Corrections and Removals of Medical
Devices and Radiation Emitting
Products
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
The Food and Drug
Administration (FDA) is announcing
that a proposed collection of
information has been submitted to the
Office of Management and Budget
SUMMARY:
VerDate Mar<15>2010
20:05 Mar 27, 2014
Jkt 232001
(OMB) for review and clearance under
the Paperwork Reduction Act of 1995.
DATES: Fax written comments on the
collection of information by April 28,
2014.
ADDRESSES: To ensure that comments on
the information collection are received,
OMB recommends that written
comments be faxed to the Office of
Information and Regulatory Affairs,
OMB, Attn: FDA Desk Officer, FAX:
202–395–7285, or emailed to oira_
submission@omb.eop.gov. All
comments should be identified with the
OMB control number 0910–0359. Also
include the FDA docket number found
in brackets in the heading of this
document.
FOR FURTHER INFORMATION CONTACT: FDA
PRA Staff, Office of Operations, Food
and Drug Administration, 1350 Piccard
Dr., PI50–400B, Rockville, MD 20850,
PRAStaff@fda.hhs.gov.
SUPPLEMENTARY INFORMATION: In
compliance with 44 U.S.C. 3507, FDA
has submitted the following proposed
collection of information to OMB for
review and clearance.
Reports of Corrections and Removals of
Medical Devices and Radiation
Emitting Products—(OMB Control
Number 0910–0359)—Extension
I. Reports of Corrections and Removals
Under § 806.10 (21 CFR 806.10), each
device manufacturer or importer shall
submit a written report to FDA of any
action initiated to correct or remove a
device to reduce a risk to health posed
by the device or to remedy a violation
of the Federal Food, Drug, and Cosmetic
Act caused by the device, which may
present a risk to health within 10
working days of initiating the correction
or removal.
Under § 806.20(a) (21 CFR 806.20(a)),
each device manufacturer or importer of
a device who initiates a correction or
removal of a device that is not required
to be reported to FDA shall keep a
record of the correction or removal.
FDA currently accepts by mail reports
of corrections and removals (806
reports) associated with medical and
radiation emitting products regulated by
the Center for Devices and Radiological
Health (CDRH) under part 806.
For general information and
assistance with 806 reports, contact the
PO 00000
Frm 00056
Fmt 4703
Sfmt 4703
CDRH Division of Small Manufacturers,
International and Consumer Assistance
(DSMICA) by telephone: 1–800–638–
2041 or 301–796–7100, or by email:
dsmica@fda.hhs.gov.
II. Proposed Electronic Submission
Process
FDA is now proposing to make
available, as a voluntary alternative to
paper submissions, an electronic
process for submitting 806 reports. The
electronic process is expected to
enhance consistency of submission data
and to speed submission processing.
Submission by mail will remain
available and will be augmented by the
new electronic submission process.
Establishing a process for using
electronic submissions does necessitate
some preparation by reporters, which
includes obtaining both: (1) A
WebTrader account and (2) a digital
verification certificate. Many other FDA
applications also utilize WebTrader. If
an applicant already has an account
with the WebTrader Electronic
Submission Gateway (ESG) and a digital
verification certificate (certificate must
be valid for 1 to 3 years), no additional
burden or cost will be incurred outside
of the time it takes to make the
submission of corrections and removals.
However, for calculating the burden for
this collection, FDA is assuming that all
respondents will be establishing a new
WebTrader account and purchasing a
digital verification certificate.
Establishing a new account for
sending electronic submissions may
take up to 2 weeks. During that time,
new reporters are advised to submit
paper reports to avoid inadvertently
missing the 10-day timeframes
associated with submission of reports
under part 806.
Upon approval of the information
collection, a submitter would go to
https://www.fda.gov/ForIndustry/
FDAeSubmitter/default.htm to submit
an 806 report via the electronic portal.
Additional information about FDA’s
ESG is posted online at https://
www.fda.gov/ForIndustry/
ElectronicSubmissionsGateway/
default.htm. You can also email
E:\FR\FM\28MRN1.SGM
28MRN1
]]>Agencies
[Federal Register Volume 79, Number 60 (Friday, March 28, 2014)]
[Notices]
[Pages 17548-17549]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2014-06931]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families
Submission for OMB Review; Comment Request
Title: Request for Specific Consent to Juvenile Court Jurisdiction.
OMB No.: 0970-0385.
Description: The William Wilberforce Trafficking Victims Protection
Reauthorization Act of 2008 (TVPRA of 2008), Public Law 110-457 was
enacted into law December 23, 2008. Section 235(d) directs the
Secretary of HHS to grant or deny requests for specific consent for
unaccompanied alien children in HHS custody who seek to invoke the
jurisdiction of a state court for a dependency order and who also seek
to invoke the jurisdiction of a state court to determine or alter his
or her custody status or release from ORR. These requests can be
extremely time sensitive since a child must ask a state court for
dependency before turning 18 years old.
In developing procedures for collecting the necessary information
from unaccompanied alien children, their attorneys, or other
representatives to allow HHS to approve or deny consent requests, ORR/
DUCS devised a form. Specifically, the form asks the requestor for his/
her identifying information, basic identifying information on the
unaccompanied alien child, the name of the HHS-funded facility where
the child is in HHS custody and care, the name of the court and its
location, and the kind of request (e.g., for a change in custody,
etc.). The form also asks that the unaccompanied alien child's attorney
or authorized representative attach a Notice of Representation, which
is an approved federal government agency form used for immigration
procedures that authorizes the attorney to act on behalf of the child
(i.e.,G-28, EOIR-28, EOIR-29), or any other form of authorization to
act on behalf of the unaccompanied alien child.
Respondents: Attorneys, accredited legal representatives, or others
authorized to act on behalf of a unaccompanied alien child.
[[Page 17549]]
Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Instrument Number of responses per hours per Total burden hours
respondents respondent response
----------------------------------------------------------------------------------------------------------------
Request for Specific Consent...... 30 1 0.33 9.9
----------------------------------------------------------------------------------------------------------------
Estimated Total Annual Burden Hours: 9.9
Additional Information: Copies of the proposed collection may be
obtained by writing to the Administration for Children and Families,
Office of Planning, Research and Evaluation, 370 L'Enfant Promenade
SW., Washington, DC 20447, Attn: ACF Reports Clearance Officer. All
requests should be identified by the title of the information
collection. Email address: infocollection@acf.hhs.gov.
OMB Comment: OMB is required to make a decision concerning the
collection of information between 30 and 60 days after publication of
this document in the Federal Register. Therefore, a comment is best
assured of having its full effect if OMB receives it within 30 days of
publication. Written comments and recommendations for the proposed
information collection should be sent directly to the following: Office
of Management and Budget,, Paperwork Reduction Project, Fax: 202-395-
7285, Email: OIRA_SUBMISSION@OMB.EOP.GOV.
Attn: Desk Officer for the Administration for Children and
Families.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 2014-06931 Filed 3-27-14; 8:45 am]
BILLING CODE 4184-01-P
