Agency Forms Undergoing Paperwork Reduction Act Review, 38185-38186 [2016-13849]
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Federal Register / Vol. 81, No. 113 / Monday, June 13, 2016 / Notices
Leroy A. Richardson,
Chief, Information Collection Review Office,
Office of Scientific Integrity, Office of the
Associate Director for Science, Office of the
Director, Centers for Disease Control and
Prevention.
[FR Doc. 2016–13847 Filed 6–10–16; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
organizations. Champions were
recognized as HA–VTE Prevention
Champions and will receive a cash
award of $10,000. A maximum of
$80,000 will now be awarded in this
challenge, an increase of $10,000.
Additional honorable mention awards
were also made to deserving entries.
Federal and international winners
received non-monetary recognition but
no prize.
Authority: 15 U.S.C. 3719.
Centers for Disease Control and
Prevention (CDC)
Dated: June 7, 2016.
Sandra Cashman,
Executive Secretary, Centers for Disease
Control and Prevention.
Requirements and Registration for
Healthcare Associated Venous
Thromboembolism Prevention
Challenge; Amendment of Notice
[FR Doc. 2016–13850 Filed 6–10–16; 8:45 am]
BILLING CODE 4163–18–P
Authority: 15 U.S.C. 3719.
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
AWARD APPROVING OFFICIAL: Thomas R.
Frieden, MD, MPH, Director, Centers for
Disease Control and Prevention, and
Administrator, Agency for Toxic
Substances and Disease Registry.
ACTION: Notice.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
The Centers for Disease
Control and Prevention (CDC) located
within the Department of Health and
Human Services (HHS) announces an
amendment to its notice entitled,
Announcement of Requirements and
Registration for Healthcare Associated
Venous Thromboembolism Prevention
Challenge. This amendment is being
made to reflect an increase in the
number of Champions and change the
maximum total prize disbursement.
There are no other changes to the
September 22, 2015 notice.
FOR FURTHER INFORMATION CONTACT:
Michele Beckman, Division of Blood
Disorders, National Center on Birth
Defects and Developmental Disabilities,
Centers for Disease Control and
Prevention, 1600 Clifton Road NE.,
Mailstop E–64, Atlanta, GA 30329,
Telephone: 404–498–6474, Fax: 404–
498–6799, Attention: HA–VTE
Prevention Challenge, Email:
havtechallenge@cdc.gov.
SUPPLEMENTARY INFORMATION:
Subject of Challenge Competition: On
September 22, 2015 CDC announced the
Requirements and Registration for
Healthcare Associated Venous
Thromboembolism Prevention
Challenge (80 FR 57187). This notice
announces an increase in the number of
Champions, from 7 to 8. The Champions
were selected from the highest scoring
U.S. hospitals, multi-hospital systems,
hospital networks, and managed care
The Centers for Disease Control and
Prevention (CDC) has submitted the
following information collection request
to the Office of Management and Budget
(OMB) for review and approval in
accordance with the Paperwork
Reduction Act of 1995. The notice for
the proposed information collection is
published to obtain comments from the
public and affected agencies.
Written comments and suggestions
from the public and affected agencies
concerning the proposed collection of
information are encouraged. Your
comments should address any of the
following: (a) Evaluate whether the
proposed collection of information is
necessary for the proper performance of
the functions of the agency, including
whether the information will have
practical utility; (b) Evaluate the
accuracy of the agencies estimate of the
burden of the proposed collection of
information, including the validity of
the methodology and assumptions used;
(c) Enhance the quality, utility, and
clarity of the information to be
collected; (d) Minimize the burden of
the collection of information on those
who are to respond, including through
the use of appropriate automated,
electronic, mechanical, or other
technological collection techniques or
other forms of information technology,
e.g., permitting electronic submission of
responses; and (e) Assess information
collection costs.
AGENCY:
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To request additional information on
the proposed project or to obtain a copy
of the information collection plan and
instruments, call (404) 639–7570 or
send an email to omb@cdc.gov. Written
comments and/or suggestions regarding
the items contained in this notice
should be directed to the Attention:
CDC Desk Officer, Office of Management
and Budget, Washington, DC 20503 or
by fax to (202) 395–5806. Written
comments should be received within 30
days of this notice.
Proposed Project
Update seat belt fit recommendation
for children—New—National Center for
Injury Prevention and Control (NCIPC),
Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
The Centers for Disease Control and
Prevention (CDC) is seeking OMB
approval to conduct a new information
collection for a study entitled, ‘‘Update
Seat Belt Fit Recommendation for
Children,’’ over a period of three years.
CDC seeks to measure how seat belts
fit children in vehicles with and
without booster seats. The scientific
basis for the current height
recommendation for when children can
transition from using a booster seat to
just a seat belt is from a 1993 study that
is outdated (Durbin et al., 2011; Reed et
al., 2013). The goal of the new collection
is to use the latest technology among the
largest sample of children to date to
help inform when children can safely
transition from using a booster seat with
a seat belt to using only a seat belt.
Findings from this data collection will
inform CDC’s child passenger safety
recommendation regarding when
children can safely transition from using
a booster seat with the seat belt to using
only the seat belt. This study will also
provide information on ways to further
reduce motor vehicle-related injuries
and deaths among children.
Prospective study participants will be
children aged 6–12 years old in the
greater District of Columbia (DC) area.
Parents of prospective study
participants will answer a series of
screening questions to determine
eligibility. Children who meet the
screening criteria and are willing to
participate will complete an in-person
measurement session. Data will be
analyzed using descriptive statistics,
mean, standard deviation, and logistic
regression. Selected findings will
eventually be published in a peerreviewed journal.
The estimated annual burden hours
are 466. There are no costs to
respondents other than their time.
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Federal Register / Vol. 81, No. 113 / Monday, June 13, 2016 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Type of respondent
Form name
Parent/guardian of children aged 6–12 years
Child participants aged 6–12 years ................
Screener Script Guide ....................................
Seat Belt Fit Measurements ..........................
Leroy A. Richardson,
Chief, Information Collection Review Office,
Office of Scientific Integrity, Office of the
Associate Director for Science, Office of the
Director, Centers for Disease Control and
Prevention.
[FR Doc. 2016–13849 Filed 6–10–16; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifiers: CMS–R–142 and
CMS–588]
Agency Information Collection
Activities: Proposed Collection;
Comment Request
Centers for Medicare &
Medicaid Services, HHS.
ACTION: Notice.
AGENCY:
The Centers for Medicare &
Medicaid Services (CMS) is announcing
an opportunity for the public to
comment on CMS’ intention to collect
information from the public. Under the
Paperwork Reduction Act of 1995 (the
PRA), federal agencies are require; to
publish notice in the Federal Register
concerning each proposed collection of
information (including each proposed
extension or reinstatement of an existing
collection of information) and to allow
60 days for public comment on the
proposed action. Interested persons are
invited to send comments regarding our
burden estimates or any other aspect of
this collection of information, including
any of the following subjects: (1) The
necessity and utility of the proposed
information collection for the proper
performance of the agency’s functions;
(2) the accuracy of the estimated
burden; (3) ways to enhance the quality,
utility, and clarity of the information to
be collected; and (4) the use of
automated collection techniques or
other forms of information technology to
minimize the information collection
burden.
DATES: Comments must be received by
August 9, 2016.
ADDRESSES: When commenting, please
reference the document identifier or
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OMB control number. To be assured
consideration, comments and
recommendations must be submitted in
any one of the following ways:
1. Electronically. You may send your
comments electronically to https://
www.regulations.gov. Follow the
instructions for ‘‘Comment or
Submission’’ or ‘‘More Search Options’’
to find the information collection
document(s) that are accepting
comments.
2. By regular mail. You may mail
written comments to the following
address: CMS, Office of Strategic
Operations and Regulatory Affairs,
Division of Regulations Development,
Attention: Document Identifier/OMB
Control Number lll, Room C4–26–
05, 7500 Security Boulevard, Baltimore,
Maryland 21244–1850.
To obtain copies of a supporting
statement and any related forms for the
proposed collection(s) summarized in
this notice, you may make your request
using one of following:
1. Access CMS’ Web site address at
https://www.cms.hhs.gov/Paperwork
ReductionActof1995.
2. Email your request, including your
address, phone number, OMB number,
and CMS document identifier, to
Paperwork@cms.hhs.gov.
3. Call the Reports Clearance Office at
(410) 786–1326.
FOR FURTHER INFORMATION CONTACT:
Reports Clearance Office at (410) 786–
1326.
SUPPLEMENTARY INFORMATION:
Contents
This notice sets out a summary of the
use and burden associated with the
following information collections. More
detailed information can be found in
each collection’s supporting statement
and associated materials (see
ADDRESSES).
CMS–R–142 Examination and
Treatment for Emergency Medical
Conditions and Women in Labor;
CMS–588 Electronic Funds Transfer
Authorization Agreement
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
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142
Number of
responses per
respondent
1
1
Average
burden per
response
(in hours)
10/60
2.5
information they conduct or sponsor.
The term ‘‘collection of information’’ is
defined in 44 U.S.C. 3502(3) and 5 CFR
1320.3(c) and includes agency requests
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
requires federal agencies to publish a
60-day notice in the Federal Register
concerning each proposed collection of
information, including each proposed
extension or reinstatement of an existing
collection of information, before
submitting the collection to OMB for
approval. To comply with this
requirement, CMS is publishing this
notice.
1. Type of Information Collection
Request: Extension of a currently
approved collection; Title of
Information Collection: Examination
and Treatment for Emergency Medical
Conditions and Women in Labor; Use:
In accordance with to regulation
sections 488.18, 489.20 and 489.24,
during Medicare surveys of hospitals
and State agencies CMS will review
hospital records for lists of on-call
physicians, and will review and obtain
the information which must be recorded
on hospital medical records for
individuals with emergency medical
conditions and women in labor, and the
emergency department reporting
information Medicare participating
hospitals and Medicare State survey
agencies must pass on to CMS.
Additionally, CMS will use the QIO
Report assessing whether an individual
had an emergency condition and
whether the individual was stabilized to
determine whether to impose a CMP or
physician exclusion sanctions. Without
such information, CMS will be unable to
make the hospital emergency services
compliance determinations that
Congress expects CMS to make under
sections 1154, 1866 and 1867 of the Act.
Form Number: CMS–R–142 (OMB
control number: 0938–0667); Frequency:
Occasionally; Affected Public: Private
Sector; Number of Respondents: 6,149;
Total Annual Responses: 6,149; Total
Annual Hours: 1. (For policy questions
regarding this collection contact Renate
Dombrowski at 410–786–4645.)
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]]>Agencies
[Federal Register Volume 81, Number 113 (Monday, June 13, 2016)]
[Notices]
[Pages 38185-38186]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-13849]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30-Day-16-16CA]
Agency Forms Undergoing Paperwork Reduction Act Review
The Centers for Disease Control and Prevention (CDC) has submitted
the following information collection request to the Office of
Management and Budget (OMB) for review and approval in accordance with
the Paperwork Reduction Act of 1995. The notice for the proposed
information collection is published to obtain comments from the public
and affected agencies.
Written comments and suggestions from the public and affected
agencies concerning the proposed collection of information are
encouraged. Your comments should address any of the following: (a)
Evaluate whether the proposed collection of information is necessary
for the proper performance of the functions of the agency, including
whether the information will have practical utility; (b) Evaluate the
accuracy of the agencies estimate of the burden of the proposed
collection of information, including the validity of the methodology
and assumptions used; (c) Enhance the quality, utility, and clarity of
the information to be collected; (d) Minimize the burden of the
collection of information on those who are to respond, including
through the use of appropriate automated, electronic, mechanical, or
other technological collection techniques or other forms of information
technology, e.g., permitting electronic submission of responses; and
(e) Assess information collection costs.
To request additional information on the proposed project or to
obtain a copy of the information collection plan and instruments, call
(404) 639-7570 or send an email to omb@cdc.gov. Written comments and/or
suggestions regarding the items contained in this notice should be
directed to the Attention: CDC Desk Officer, Office of Management and
Budget, Washington, DC 20503 or by fax to (202) 395-5806. Written
comments should be received within 30 days of this notice.
Proposed Project
Update seat belt fit recommendation for children--New--National
Center for Injury Prevention and Control (NCIPC), Centers for Disease
Control and Prevention (CDC).
Background and Brief Description
The Centers for Disease Control and Prevention (CDC) is seeking OMB
approval to conduct a new information collection for a study entitled,
``Update Seat Belt Fit Recommendation for Children,'' over a period of
three years.
CDC seeks to measure how seat belts fit children in vehicles with
and without booster seats. The scientific basis for the current height
recommendation for when children can transition from using a booster
seat to just a seat belt is from a 1993 study that is outdated (Durbin
et al., 2011; Reed et al., 2013). The goal of the new collection is to
use the latest technology among the largest sample of children to date
to help inform when children can safely transition from using a booster
seat with a seat belt to using only a seat belt.
Findings from this data collection will inform CDC's child
passenger safety recommendation regarding when children can safely
transition from using a booster seat with the seat belt to using only
the seat belt. This study will also provide information on ways to
further reduce motor vehicle-related injuries and deaths among
children.
Prospective study participants will be children aged 6-12 years old
in the greater District of Columbia (DC) area. Parents of prospective
study participants will answer a series of screening questions to
determine eligibility. Children who meet the screening criteria and are
willing to participate will complete an in-person measurement session.
Data will be analyzed using descriptive statistics, mean, standard
deviation, and logistic regression. Selected findings will eventually
be published in a peer-reviewed journal.
The estimated annual burden hours are 466. There are no costs to
respondents other than their time.
[[Page 38186]]
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Type of respondent Form name Number of responses per per response
respondents respondent (in hours)
----------------------------------------------------------------------------------------------------------------
Parent/guardian of children aged 6-12 Screener Script Guide... 667 1 10/60
years.
Child participants aged 6-12 years.... Seat Belt Fit 142 1 2.5
Measurements.
----------------------------------------------------------------------------------------------------------------
Leroy A. Richardson,
Chief, Information Collection Review Office, Office of Scientific
Integrity, Office of the Associate Director for Science, Office of the
Director, Centers for Disease Control and Prevention.
[FR Doc. 2016-13849 Filed 6-10-16; 8:45 am]
BILLING CODE 4163-18-P
