Proposed Data Collection Submitted for Public Comment and Recommendations, 58912-58913 [2021-23186]
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58912
Federal Register / Vol. 86, No. 203 / Monday, October 25, 2021 / Notices
Local Exchange Carriers, CC Docket No.
01–338 and WC Docket No. 04–313,
Order on Remand.
Form Number: N/A.
Type of Review: Extension of a
currently approved collection.
Respondents: Business or other forprofit entities, Not-for-profit institutions
and State, Local or Tribal government.
Number of Respondents and
Reponses: 645 respondents; 645
responses.
Estimated Time per Response: 8
hours.
Frequency of Response:
Recordkeeping requirement, third party
disclosure requirement and on occasion
reporting requirement.
Obligation to Respond: Required to
obtain or retain benefits. Statutory
authority for this information collection
is contained in 47 U.S.C. Section 251 of
the Communications Act of 1934, as
amended.
Total Annual Burden: 5,160 hours.
Total Annual Cost: No Cost.
Privacy Act Impact Assessment: No
impact(s).
Nature and Extent of Confidentiality:
The Commission is not requesting
respondents to submit or disclose
confidential information. However, in
certain circumstances, respondents may
voluntarily choose to submit
confidential information pursuant to
applicable confidentiality rules.
Needs and Uses: In the Order on
Remand, the Commission imposed
unbundling obligations in a more
targeted manner where requesting
carriers have undertaken their own
facilities-based investments and will be
using UNEs (unbundled network
elements) in conjunction with selfprovisioned facilities. The Commission
also eliminated the subdelegation of
authority to state commissions adopted
in the previous order. Prior to the
issuance of the Order, the Commission
sought comment on issues relating to
combinations of UNEs, called
‘‘enhanced extended links’’ (EELs), in
order to effectively tailor access to EELs
to those carriers seeking to provide
significant local usage to end users. In
the Order, the Commission adopted
three specific service eligibility criteria
for access to EELs in accordance with
Commission rules.
Federal Communications Commission.
Katura Jackson,
Federal Register Liaison Officer.
[FR Doc. 2021–23145 Filed 10–22–21; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–22–22AD; Docket No. CDC–2021–
0113]
Proposed Data Collection Submitted
for Public Comment and
Recommendations
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
ACTION: Notice with comment period.
AGENCY:
The Centers for Disease
Control and Prevention (CDC), as part of
its continuing effort to reduce public
burden and maximize the utility of
government information, invites the
general public and other Federal
agencies to take this opportunity to
comment on proposed information
collections, as required by the
Paperwork Reduction Act of 1995. This
notice invites comment on the Research
Data Center (RDC) Proposal for Access
to Confidential Data for the National
Center for Health Statistics (NCHS). The
proposed collection will be used to
assess researcher’s requests for access to
confidential NCHS data for their
research projects.
DATES: Written comments must be
received on or before December 27,
2021.
SUMMARY:
You may submit comments,
identified by Docket No. CDC–2021–
0113 by any of the following methods:
• Federal eRulemaking Portal:
Regulations.gov. Follow the instructions
for submitting comments.
• Mail: Jeffrey M. Zirger, Information
Collection Review Office, Centers for
Disease Control and Prevention, 1600
Clifton Road NE, MS H21–8, Atlanta,
Georgia 30329.
Instructions: All submissions received
must include the agency name and
Docket Number. All relevant comments
received will be posted without change
to Regulations.gov, including any
personal information provided. For
access to the docket to read background
documents or comments received, go to
Regulations.gov.
Please note: All public comment
should be submitted through the
Federal eRulemaking portal
(regulations.gov) or by U.S. mail to the
address listed above.
FOR FURTHER INFORMATION CONTACT: To
request more information on the
proposed project or to obtain a copy of
the information collection plan and
instruments, contact Jeffrey M. Zirger,
ADDRESSES:
PO 00000
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Information Collection Review Office,
Centers for Disease Control and
Prevention, 1600 Clifton Road NE, MS–
H21–8, Atlanta, Georgia 30329; phone:
404–639–7570; Email: omb@cdc.gov.
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. In addition, the PRA also
requires Federal agencies to provide a
60-day notice in the Federal Register
concerning each proposed collection of
information, including each new
proposed collection, each proposed
extension of existing collection of
information, and each reinstatement of
previously approved information
collection before submitting the
collection to OMB for approval. To
comply with this requirement, we are
publishing this notice of a proposed
data collection as described below.
The OMB is particularly interested in
comments that will help:
1. 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;
2. Evaluate the accuracy of the
agency’s estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used;
3. Enhance the quality, utility, and
clarity of the information to be
collected;
4. 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 submissions
of responses; and
5. Assess information collection costs.
Proposed Project
Research Data Center (RDC) Proposal
for Access to Confidential Data for the
National Center for Health Statistics—
Existing Collection in use without an
OMB Control Number—National Center
for Health Statistics (NCHS), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
Section 306(b)(4) of the Public Health
Service (PHS) Act (42 U.S.C. 242k(b)(4)),
as amended, authorizes that the
Secretary of Health and Human Services
(DHHS), acting through NCHS, receive
requests for providing data and statistics
to the public. NCHS receives requests
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58913
Federal Register / Vol. 86, No. 203 / Monday, October 25, 2021 / Notices
for confidential data from the public
through the Research Data Center (RDC)
Proposal for Access to Confidential
Data. This is a request for approval from
OMB to collect information via the RDC
proposal over the next three years.
As part of a comprehensive data
dissemination program, the Research
Data Center (RDC), National Center for
Health Statistics (NCHS), Centers for
Disease Control and Prevention (CDC),
requires prospective researchers who
need access to confidential data to
adjudication on whether the proposed
research is possible.
To capture the information needed to
adjudicate researchers’ need for access
to confidential NCHS data, CDC
requests OMB approval for a total
estimated annual burden total of 330
hours (990 hours for a three-year
clearance period). The resulting
information will be for NCHS internal
use. There is no cost to respondents
other than their time to complete the
proposal.
complete a research proposal.
Researchers self-select whether they
need access to confidential data to
answer their research questions. The
RDC requires the researcher to complete
a research proposal so NCHS
understands the research proposed,
whether confidential data are available
to address the research questions, how
the confidential data will be used, and
what data outputs the researcher needs
to satisfy their project. The completed
proposal is sent to NCHS for
ESTIMATED ANNUALIZED BURDEN HOURS
Avg. burden
per response
(in hrs.)
Total burden
(in hrs.)
Form name
Researcher ........................................
Research Data Center proposal ......
110
1
3
330
Total ...........................................
...........................................................
........................
........................
........................
330
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2021–23186 Filed 10–22–21; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
Advisory Board on Radiation and
Worker Health (ABRWH), National
Institute for Occupational Safety and
Health (NIOSH)
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
AGENCY:
Notice of meeting and request
for comment.
ACTION:
In accordance with the
Federal Advisory Committee Act, the
CDC announces the following meeting
of the Advisory Board on Radiation and
Worker Health (ABRWH or the Advisory
Board). This meeting is open to the
public, limited only by the number of
audio conference lines and internet
conference accesses available, which is
200 combined. The public is welcome to
submit written comments in advance of
the meeting, to the contact person
below. Written comments received in
advance of the meeting will be included
in the official record of the meeting. The
public is also welcomed to listen to the
meeting by joining a teleconference line
and/or computer connection
(information below).
SUMMARY:
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Number of
responses per
respondent
Number of
respondents
Type of respondents
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18:00 Oct 22, 2021
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The meeting will be held on
December 8, 2021, from 1:00 p.m. to
6:00 p.m., EST, and December 9, 2021,
from 1:00 p.m. to 4:00 p.m., EST. A
public comment session will be held on
December 8, 2021 at 5:00 p.m., EST, and
will conclude at 6:00 p.m., EST, or
following the final call for public
comment, whichever comes first.
Written comments must be received
on or before December 1, 2021.
ADDRESSES: You may submit comments
by mail to: Sherri Diana, National
Institute for Occupational Safety and
Health, 1090 Tusculum Avenue, MS C–
34, Cincinnati, Ohio 45226.
Meeting Information: The USA tollfree dial-in numbers are: +1 669 254
5252 US (San Jose); +1 646 828 7666 US
(New York); +1 551 285 1373 US; +1
669 216 1590 US (San Jose); The
Meeting ID is: 161 731 2093 and the
Passcode is: 45481965; Web conference
by Zoom meeting connection: https://
cdc.zoomgov.com/j/1617312093?pwd=
eDREUG5JaGl6Y1Z2YUVyNnJmYll
HUT09.
FOR FURTHER INFORMATION CONTACT:
Rashaun Roberts, Ph.D., Designated
Federal Officer, NIOSH, CDC, 1090
Tusculum Avenue, Mailstop C–24,
Cincinnati, Ohio 45226, Telephone:
(513) 533–6800, Toll Free: 1(800) CDC–
INFO, Email: ocas@cdc.gov.
SUPPLEMENTARY INFORMATION:
Background: The Advisory Board was
established under the Energy Employees
Occupational Illness Compensation
Program Act of 2000 to advise the
President on a variety of policy and
technical functions required to
implement and effectively manage the
new compensation program. Key
functions of the Advisory Board include
DATES:
PO 00000
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providing advice on the development of
probability of causation guidelines
which have been promulgated by the
Department of Health and Human
Services (HHS) as a final rule, advice on
methods of dose reconstruction which
have also been promulgated by HHS as
a final rule, advice on the scientific
validity and quality of dose estimation
and reconstruction efforts being
performed for purposes of the
compensation program, and advice on
petitions to add classes of workers to the
Special Exposure Cohort (SEC). In
December 2000, the President delegated
responsibility for funding, staffing, and
operating the Advisory Board to HHS,
which subsequently delegated this
authority to the CDC. NIOSH
implements this responsibility for CDC.
The Advisory Board’s charter was
issued on August 3, 2001, renewed at
appropriate intervals, rechartered on
March 22, 2020, and will terminate on
March 22, 2022.
Purpose: The Advisory Board is
charged with (a) providing advice to the
Secretary, HHS, on the development of
guidelines under Executive Order
13179; (b) providing advice to the
Secretary, HHS, on the scientific
validity and quality of dose
reconstruction efforts performed for this
program; and (c) upon request by the
Secretary, HHS, advising the Secretary
on whether there is a class of employees
at any Department of Energy facility
who were exposed to radiation but for
whom it is not feasible to estimate their
radiation dose, and on whether there is
reasonable likelihood that such
radiation doses may have endangered
the health of members of this class.
E:\FR\FM\25OCN1.SGM
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[Federal Register Volume 86, Number 203 (Monday, October 25, 2021)]
[Notices]
[Pages 58912-58913]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2021-23186]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-22-22AD; Docket No. CDC-2021-0113]
Proposed Data Collection Submitted for Public Comment and
Recommendations
AGENCY: Centers for Disease Control and Prevention (CDC), Department of
Health and Human Services (HHS).
ACTION: Notice with comment period.
-----------------------------------------------------------------------
SUMMARY: The Centers for Disease Control and Prevention (CDC), as part
of its continuing effort to reduce public burden and maximize the
utility of government information, invites the general public and other
Federal agencies to take this opportunity to comment on proposed
information collections, as required by the Paperwork Reduction Act of
1995. This notice invites comment on the Research Data Center (RDC)
Proposal for Access to Confidential Data for the National Center for
Health Statistics (NCHS). The proposed collection will be used to
assess researcher's requests for access to confidential NCHS data for
their research projects.
DATES: Written comments must be received on or before December 27,
2021.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2021-
0113 by any of the following methods:
Federal eRulemaking Portal: Regulations.gov. Follow the
instructions for submitting comments.
Mail: Jeffrey M. Zirger, Information Collection Review
Office, Centers for Disease Control and Prevention, 1600 Clifton Road
NE, MS H21-8, Atlanta, Georgia 30329.
Instructions: All submissions received must include the agency name
and Docket Number. All relevant comments received will be posted
without change to Regulations.gov, including any personal information
provided. For access to the docket to read background documents or
comments received, go to Regulations.gov.
Please note: All public comment should be submitted through the
Federal eRulemaking portal (regulations.gov) or by U.S. mail to the
address listed above.
FOR FURTHER INFORMATION CONTACT: To request more information on the
proposed project or to obtain a copy of the information collection plan
and instruments, contact Jeffrey M. Zirger, Information Collection
Review Office, Centers for Disease Control and Prevention, 1600 Clifton
Road NE, MS-H21-8, Atlanta, Georgia 30329; phone: 404-639-7570; Email:
[email protected].
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. In addition, the PRA also requires
Federal agencies to provide a 60-day notice in the Federal Register
concerning each proposed collection of information, including each new
proposed collection, each proposed extension of existing collection of
information, and each reinstatement of previously approved information
collection before submitting the collection to OMB for approval. To
comply with this requirement, we are publishing this notice of a
proposed data collection as described below.
The OMB is particularly interested in comments that will help:
1. 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;
2. Evaluate the accuracy of the agency's estimate of the burden of
the proposed collection of information, including the validity of the
methodology and assumptions used;
3. Enhance the quality, utility, and clarity of the information to
be collected;
4. 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
submissions of responses; and
5. Assess information collection costs.
Proposed Project
Research Data Center (RDC) Proposal for Access to Confidential Data
for the National Center for Health Statistics--Existing Collection in
use without an OMB Control Number--National Center for Health
Statistics (NCHS), Centers for Disease Control and Prevention (CDC).
Background and Brief Description
Section 306(b)(4) of the Public Health Service (PHS) Act (42 U.S.C.
242k(b)(4)), as amended, authorizes that the Secretary of Health and
Human Services (DHHS), acting through NCHS, receive requests for
providing data and statistics to the public. NCHS receives requests
[[Page 58913]]
for confidential data from the public through the Research Data Center
(RDC) Proposal for Access to Confidential Data. This is a request for
approval from OMB to collect information via the RDC proposal over the
next three years.
As part of a comprehensive data dissemination program, the Research
Data Center (RDC), National Center for Health Statistics (NCHS),
Centers for Disease Control and Prevention (CDC), requires prospective
researchers who need access to confidential data to complete a research
proposal. Researchers self-select whether they need access to
confidential data to answer their research questions. The RDC requires
the researcher to complete a research proposal so NCHS understands the
research proposed, whether confidential data are available to address
the research questions, how the confidential data will be used, and
what data outputs the researcher needs to satisfy their project. The
completed proposal is sent to NCHS for adjudication on whether the
proposed research is possible.
To capture the information needed to adjudicate researchers' need
for access to confidential NCHS data, CDC requests OMB approval for a
total estimated annual burden total of 330 hours (990 hours for a
three-year clearance period). The resulting information will be for
NCHS internal use. There is no cost to respondents other than their
time to complete the proposal.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Avg. burden
Type of respondents Form name Number of responses per per response Total burden
respondents respondent (in hrs.) (in hrs.)
----------------------------------------------------------------------------------------------------------------
Researcher.................... Research Data 110 1 3 330
Center proposal.
---------------------------------------------------------------
Total..................... ................ .............. .............. .............. 330
----------------------------------------------------------------------------------------------------------------
Jeffrey M. Zirger,
Lead, Information Collection Review Office, Office of Scientific
Integrity, Office of Science, Centers for Disease Control and
Prevention.
[FR Doc. 2021-23186 Filed 10-22-21; 8:45 am]
BILLING CODE 4163-18-P
