Agency Forms Undergoing Paperwork Reduction Act Review, 62740-62741 [2016-21885]
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62740
Federal Register / Vol. 81, No. 176 / Monday, September 12, 2016 / Notices
valid assumptions and methodology;
ways to enhance the quality, utility, and
clarity of the information to be
collected; and ways in which we can
minimize the burden of the collection of
information on those who are to
respond, through the use of appropriate
technological collection techniques or
other forms of information technology.
OBTAINING COPIES OF PROPOSALS:
Requesters may obtain a copy of the
information collection documents from
the General Services Administration
(GSA), Regulatory Secretariat Division
(MVCB), 1800 F Street NW.,
Washington, DC 20405, telephone 202–
501–4755. Please cite OMB Control No.
9000–0095, Commerce Patent
Regulations, in all correspondence.
Dated: September 6, 2016.
Lorin S. Curit,
Director, Federal Acquisition Policy Division,
Office of Governmentwide Acquisition Policy,
Office of Acquisition Policy, Office of
Governmentwide Policy.
[FR Doc. 2016–21790 Filed 9–9–16; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–16–0852]
Agency Forms Undergoing Paperwork
Reduction Act Review
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
ACTION: Notice with comment period;
withdrawal.
AGENCY:
The Centers for Disease
Control and Prevention (CDC) in the
Department of Health and Human
Services (HHS) announces the
withdrawal of the notice published
under the same title on August 25, 2016
for public comment.
DATES: Effective September 12, 2016.
FOR FURTHER INFORMATION CONTACT:
Information Collection Review Office,
Centers for Disease Control and
Prevention, 1600 Clifton Road NE., MS–
D74, Atlanta, Georgia 30329; phone:
404–639–7570; Email: omb@cdc.gov.
SUPPLEMENTARY INFORMATION: On August
25, 2016 CDC published a notice in the
Federal Register titled ‘‘Agency Forms
Undergoing Paperwork Reduction Act
Review’’ (Vol. 81, No. 165 FR Doc.
2016–20366, Pages 58513–58514). This
notice was published prematurely and
inadvertently. The notice is being
withdrawn immediately for public
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SUMMARY:
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comment. A new notice will be
published at a later date for public
comment.
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. 2016–21884 Filed 9–9–16; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–16–16ARH]
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. Direct
written comments and/or suggestions
regarding the items contained in this
notice to the Attention: CDC Desk
Officer, Office of Management and
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Budget, Washington, DC 20503 or by fax
to (202) 395–5806. Written comments
should be received within 30 days of
this notice.
Proposed Project
Poison Center Collaborations for
Public Health Emergencies—NEW—
National Center for Environmental
Health (NCEH), Centers for Disease
Control and Prevention (CDC).
Background and Brief Description
Centers for Disease Control and
Prevention (CDC) is requesting a threeyear approval for a new generic
information collection request (Generic
ICR) plan titled ‘‘Poison Center
Collaborations for Public Health
Emergencies.’’
CDC’s key partner, the American
Association of Poison Control Centers
(AAPCC), is a national network of 55
poison centers working to prevent and
treat poison exposures. The goal for this
new Generic ICR is to create a timely
mechanism to allow poison centers, in
collaboration with CDC, to obtain
critical exposure and health information
during public health emergencies. This
information is not captured during
initial poison center calls about triage
and treatment of potential poison
exposures. Additional data collections
are needed quickly to further
characterize exposures, risk factors, and
illnesses.
When a public health emergency of
interest to CDC and AAPCC occurs, the
CDC and AAPCC hold a meeting to
mutually decide whether the incident
needs further investigation. For a public
health emergency to be selected for callback, adverse health effects must have
occurred and a response is needed to
prevent further morbidity and mortality.
The event must meet the criteria below:
(1) The event is a public health
emergency causing adverse health
effects.
(2) Timely data are urgently needed to
inform rapid public health action to
prevent or reduce injury, disease, or
death.
(3) The event is characterized by a
natural or man-made disaster,
contaminated food or water, a new or
existing consumer product, or an
emerging public health threat.
(4) The event has resulted in calls to
a poison center, and the poison center
agrees to conduct the call-back data
collection.
(5) The event is domestic.
(6) Data collection will be completed
in 60 days or less.
Trained poison center staff will
conduct the call-back telephone survey,
after administering consent.
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62741
Federal Register / Vol. 81, No. 176 / Monday, September 12, 2016 / Notices
Respondents will include individuals
who call poison centers about exposures
related to the select public health
emergencies. These respondents include
adults, 18 years and older; adolescents,
15 to less than 18 years; and parents or
guardians on behalf of their children
less than 15 years of age.
The total estimate of 300 annual
respondents is based on poison center
experience which assumes two
incidents per year with approximately
150 respondents per event. The average
burden per respondent is approximately
40 minutes for the call-back
questionnaire. We anticipate a total
annualized burden of 200 hours.
There is no cost to the respondents
other than their time.
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Type of respondent
Form name
Adult Poison Center Callers ...........................
Adolescent Poison Center Callers ..................
Parent or Guardian Poison Center Callers .....
Sample Questionnaire—Adults ......................
Sample Questionnaire—Adolescent ..............
Sample Questionnaire—Parent or Guardian
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. 2016–21885 Filed 9–9–16; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifiers: CMS–588, CMS–
10146, CMS–10185, CMS–10261, and CMS–
10631]
Agency Information Collection
Activities: Submission for OMB
Review; 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
(PRA), federal agencies are required 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
a second opportunity for public
comment on the notice. Interested
persons are invited to send comments
regarding the burden estimate or any
other aspect of this collection of
information, including any of the
following subjects: The necessity and
utility of the proposed information
collection for the proper performance of
the agency’s functions; the accuracy of
the estimated burden; ways to enhance
the quality, utility, and clarity of the
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SUMMARY:
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18:40 Sep 09, 2016
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information to be collected; and the use
of automated collection techniques or
other forms of information technology to
minimize the information collection
burden.
DATES: Comments on the collection(s) of
information must be received by the
OMB desk officer by October 12, 2016.
ADDRESSES: When commenting on the
proposed information collections,
please reference the document identifier
or OMB control number. To be assured
consideration, comments and
recommendations must be received by
the OMB desk officer via one of the
following transmissions: OMB, Office of
Information and Regulatory Affairs,
Attention: CMS Desk Officer, Fax
Number: (202) 395–5806, OR, Email:
OIRA_submission@omb.eop.gov.
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/
PaperworkReductionActof1995.
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: Under the
Paperwork Reduction Act of 1995 (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. 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
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210
30
60
Number of
responses per
respondent
1
1
1
Average
burden per
response
(in hours)
40/60
40/60
40/60
information to a third party. Section
3506(c)(2)(A) of the PRA (44 U.S.C.
3506(c)(2)(A)) requires federal agencies
to publish a 30-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 that summarizes
the following proposed collection(s) of
information for public comment:
1. Type of Information Collection
Request: Revision of a currently
approved collection; Title of
Information Collection: Electronic
Funds Transfer Authorization
Agreement; Use: The information is
needed to allow providers to receive
funds electronically in their bank
accounts. Form Number: CMS–588
(OMB control number: 0938–0626);
Frequency: On occasion; Affected
Public: Business or other for-profit, Notfor-profit institutions; Number of
Respondents: 45,807; Total Annual
Responses: 45,807; Total Annual Hours:
22,906. (For policy questions regarding
this collection contact Kimberly
McPhillips at 410–786–4645.)
2. Type of Information Collection
Request: Revision of a currently
approved collection; Title of
Information Collection: Medicare Part D
Reporting Requirements and Supporting
Regulations; Use: Data collected via
Medicare Part D Reporting
Requirements will be an integral
resource for oversight, monitoring,
compliance and auditing activities
necessary to ensure quality provision of
the Medicare Prescription Drug Benefit
to beneficiaries. For all reporting
sections, data are reported electronically
to CMS. Each reporting section is
reported at one of the following levels:
Contract (data should be entered at the
H#, S#, R#, or E# level) or Plan (data
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]]>Agencies
[Federal Register Volume 81, Number 176 (Monday, September 12, 2016)]
[Notices]
[Pages 62740-62741]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-21885]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30Day-16-16ARH]
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. Direct written comments
and/or suggestions regarding the items contained in this notice 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
Poison Center Collaborations for Public Health Emergencies--NEW--
National Center for Environmental Health (NCEH), Centers for Disease
Control and Prevention (CDC).
Background and Brief Description
Centers for Disease Control and Prevention (CDC) is requesting a
three-year approval for a new generic information collection request
(Generic ICR) plan titled ``Poison Center Collaborations for Public
Health Emergencies.''
CDC's key partner, the American Association of Poison Control
Centers (AAPCC), is a national network of 55 poison centers working to
prevent and treat poison exposures. The goal for this new Generic ICR
is to create a timely mechanism to allow poison centers, in
collaboration with CDC, to obtain critical exposure and health
information during public health emergencies. This information is not
captured during initial poison center calls about triage and treatment
of potential poison exposures. Additional data collections are needed
quickly to further characterize exposures, risk factors, and illnesses.
When a public health emergency of interest to CDC and AAPCC occurs,
the CDC and AAPCC hold a meeting to mutually decide whether the
incident needs further investigation. For a public health emergency to
be selected for call-back, adverse health effects must have occurred
and a response is needed to prevent further morbidity and mortality.
The event must meet the criteria below:
(1) The event is a public health emergency causing adverse health
effects.
(2) Timely data are urgently needed to inform rapid public health
action to prevent or reduce injury, disease, or death.
(3) The event is characterized by a natural or man-made disaster,
contaminated food or water, a new or existing consumer product, or an
emerging public health threat.
(4) The event has resulted in calls to a poison center, and the
poison center agrees to conduct the call-back data collection.
(5) The event is domestic.
(6) Data collection will be completed in 60 days or less.
Trained poison center staff will conduct the call-back telephone
survey, after administering consent.
[[Page 62741]]
Respondents will include individuals who call poison centers about
exposures related to the select public health emergencies. These
respondents include adults, 18 years and older; adolescents, 15 to less
than 18 years; and parents or guardians on behalf of their children
less than 15 years of age.
The total estimate of 300 annual respondents is based on poison
center experience which assumes two incidents per year with
approximately 150 respondents per event. The average burden per
respondent is approximately 40 minutes for the call-back questionnaire.
We anticipate a total annualized burden of 200 hours.
There is no cost to the respondents other than their time.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Type of respondent Form name Number of responses per per response
respondents respondent (in hours)
----------------------------------------------------------------------------------------------------------------
Adult Poison Center Callers........... Sample Questionnaire-- 210 1 40/60
Adults.
Adolescent Poison Center Callers...... Sample Questionnaire-- 30 1 40/60
Adolescent.
Parent or Guardian Poison Center Sample Questionnaire-- 60 1 40/60
Callers. Parent or Guardian.
----------------------------------------------------------------------------------------------------------------
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. 2016-21885 Filed 9-9-16; 8:45 am]
BILLING CODE 4163-18-P
