Proposed Data Collection Submitted for Public Comment and Recommendations, 67544-67546 [2020-23454]
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Federal Register / Vol. 85, No. 206 / Friday, October 23, 2020 / Notices
These estimates include any time
spent by separately incorporated
subsidiaries and other entities affiliated
with the ultimate parent companies that
receive the information requests.
Estimated Average Burden per Year
Per Request: 196 hours.
(a) Information requests to the four
largest recipients 6 of the Commission’s
information request, at a per request
average each year of 400 hours = 2,400
hours, cumulatively, per year; and
(b) Information requests to nine
additional respondents, of smaller size,
at a per request average each year of 60
hours = 540 hours, cumulatively, per
year.
Estimated Annual Labor Cost:
$294,000.
Estimated Capital or Other Non-Labor
Cost: de minimis.
Request for Comment
Your comment—including your name
and your state—will be placed on the
public record of this proceeding.
Because your comment will be made
public, you are solely responsible for
making sure that your comment does
not include any sensitive personal
information, such as anyone’s Social
Security number; date of birth; driver’s
license number or other state
identification number, or foreign
country equivalent; passport number;
financial account number; or credit or
debit card number. You are also solely
responsible for making sure that your
comment does not include any sensitive
health information, such as medical
records or other individually
identifiable health information. In
addition, your comment should not
include any ‘‘trade secret or any
commercial or financial information
which . . . is privileged or
confidential’’—as provided by Section
6(f) of the FTC Act, 15 U.S.C. 46(f), and
FTC Rule 4.10(a)(2), 16 CFR 4.10(a)(2)—
including in particular competitively
sensitive information such as costs,
sales statistics, inventories, formulas,
patterns, devices, manufacturing
processes, or customer names.
Josephine Liu,
Assistant General Counsel for Legal Counsel.
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[FR Doc. 2020–23515 Filed 10–22–20; 8:45 am]
BILLING CODE 6750–01–P
collection of information during that period,
including . . . separately incorporated subsidiaries
or affiliates.’’).
6 There are two tobacco companies that receive
both a cigarette Order and a smokeless tobacco
Order. Thus, this would equate to six requests for
burden analysis.
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18:09 Oct 22, 2020
Jkt 253001
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–21–0728; Docket No. CDC–2020–
0096]
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 the opportunity to comment on
a proposed and/or continuing
information collection, as required by
the Paperwork Reduction Act of 1995.
This notice invites comment on a
proposed information collection project
titled National Notifiable Diseases
Surveillance System—Revision—Center
for Surveillance, Epidemiology and
Laboratory Services (CSELS), Centers for
Disease Control and Prevention (CDC).
The purpose of this data collection is to
provide the official source of statistics
in the United States for nationally
notifiable conditions. Data will be used
to monitor the occurrence and spread of
nationally notifiable conditions. Data
will be gathered through electronic
submissions of case notifications to CDC
from public health departments from 50
states, New York City, Washington DC,
five U.S. territories, and three freely
associated states.
DATES: CDC must receive written
comments on or before December 22,
2020.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2020–
0096 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–D74, Atlanta,
Georgia 30329.
Instructions: All submissions received
must include the agency name and
Docket Number. CDC will post, without
change, all relevant comments to
Regulations.gov.
Please note: Submit all comments
through the Federal eRulemaking portal
(regulations.gov) or by U.S. mail to the
address listed above.
SUMMARY:
PO 00000
Frm 00037
Fmt 4703
Sfmt 4703
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–
D74, Atlanta, Georgia 30329; phone:
404–639–7118; 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 the 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; and
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.
5. Assess information collection costs.
FOR FURTHER INFORMATION CONTACT:
Proposed Project
National Notifiable Diseases
Surveillance System (OMB Control No.
0920–0728, Exp. 04/30/2023)—
Revision—Center for Surveillance,
Epidemiology and Laboratory Services
(CSELS), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
The Public Health Services Act (42
U.S.C. 241) authorizes CDC to
E:\FR\FM\23OCN1.SGM
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Federal Register / Vol. 85, No. 206 / Friday, October 23, 2020 / Notices
disseminate nationally notifiable
condition information. The National
Notifiable Diseases Surveillance System
(NNDSS) is based on data collected at
the state, territorial and local levels as
a result of legislation and regulations in
those jurisdictions that require health
care providers, medical laboratories,
and other entities to submit healthrelated data on reportable conditions to
public health departments. These
reportable conditions, which include
infectious and non-infectious diseases,
vary by jurisdiction depending upon
each jurisdiction’s health priorities and
needs. Each year, the Council of State
and Territorial Epidemiologists (CSTE),
supported by CDC, determines which
reportable conditions should be
designated nationally notifiable or
under standardized surveillance.
CDC requests a three-year approval for
a Revision for the NNDSS (OMB Control
No. 0920–0728, Expiration Date 04/30/
2023). This Revision includes requests
for approval to: (1) Receive case
notification data for Multisystem
Inflammatory Syndrome (MIS)
associated with Coronavirus Disease
2019 (COVID–19); (2) receive new
disease-specific data elements for
Anthrax, Brucellosis,
Campylobacteriosis, Cholera,
Cryptosporidiosis, Hansen’s Disease,
Leptospirosis, Melioidosis, MIS
associated with COVID–19, COVID–19,
S. Paratyphi Infection, S. Typhi
Infection, Salmonellosis, STEC,
Shigellosis, and Vibriosis; and (3)
Receive new vaccine-related data
elements for all conditions.
The NNDSS currently facilitates the
submission and aggregation of case
notification data voluntarily submitted
to CDC from 60 jurisdictions: public
health departments in every U.S. state,
New York City, Washington DC, five
available through CDC WONDER and
data.cdc.gov. Annual summaries of
finalized nationally notifiable disease
data are published on CDC WONDER
and data.cdc.gov and disease-specific
data are published by individual CDC
programs.
The burden estimates include the
number of hours that the public health
department uses to process and send
case notification data from their
jurisdiction to CDC. Specifically, the
burden estimates include separate
burden hours incurred for automated
and non-automated transmissions,
separate weekly burden hours incurred
for modernizing surveillance systems as
part of NNDSS Modernization Initiative
(NMI) implementation, separate burden
hours incurred for annual data
reconciliation and submission, and
separate one-time burden hours
incurred for the addition of new
diseases and data elements. The burden
estimates for the one-time burden for
reporting jurisdictions are for the
addition of case notification data for
MIS associated with COVID–19; diseasespecific data elements for Anthrax,
Brucellosis, Campylobacteriosis,
Cholera, Cryptosporidiosis, Hansen’s
Disease, Leptospirosis, Melioidosis, MIS
associated with COVID–19, COVID–19,
S. Paratyphi Infection, S. Typhi
Infection, Salmonellosis, STEC,
Shigellosis, and Vibriosis; and vaccine
data elements for all diseases. The
estimated annual burden for the 257
respondents is 18,954 hours. The cost of
the information collection is $830,400.
The total burden hours increased from
18,414 to 18,954 since the last revision
because there were more diseasespecific data elements added in this
revision as compared to the last
revision.
U.S. territories (American Samoa, the
Commonwealth of Northern Mariana
Islands, Guam, Puerto Rico, and the U.S.
Virgin Islands), and three freely
associated states (Federated States of
Micronesia, the Republic of the
Marshall Islands, and the Republic of
Palau). This information is shared
across jurisdictional boundaries and
both surveillance and prevention and
control activities are coordinated at
regional and national levels.
Approximately 90% of case
notifications are encrypted and
submitted to NNDSS electronically from
already existing databases by automated
electronic messages. When automated
transmission is not possible, case
notifications are faxed, emailed,
uploaded to a secure network or entered
into a secure website. All case
notifications that are faxed or emailed
are done so in the form of an aggregate
weekly or annual report, not individual
cases. These different mechanisms used
to send case notifications to CDC vary
by the jurisdiction and the disease or
condition. Jurisdictions remove most
personally identifiable information (PII)
before data are submitted to CDC, but
some data elements (e.g., date of birth,
date of diagnosis, county of residence)
could potentially be combined with
other information to identify
individuals. Private information is not
disclosed unless otherwise compelled
by law. All data are treated in a secure
manner consistent with the technical,
administrative, and operational controls
required by the Federal Information
Security Management Act of 2002
(FISMA) and the 2010 National Institute
of Standards and Technology (NIST)
Recommended Security Controls for
Federal Information Systems and
Organizations. Weekly tables of
nationally notifiable diseases are
ESTIMATED ANNUALIZED BURDEN HOURS
Type of respondent
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States
States
States
States
States
................................................
................................................
................................................
................................................
................................................
Territories
Territories
Territories
Territories
Territories
..........................................
..........................................
..........................................
..........................................
..........................................
Freely Associated States ..................
Freely Associated States ..................
Freely Associated States ..................
VerDate Sep<11>2014
18:09 Oct 22, 2020
Weekly (Automated) .........................
Weekly (Non-automated) .................
Weekly (NMI Implementation) ..........
Annual ..............................................
One-time Addition of Diseases and
Data Elements.
Weekly (Automated) .........................
Weekly, Quarterly (Non-automated)
Weekly (NMI Implementation) ..........
Annual ..............................................
One-time Addition of Diseases and
Data Elements.
Weekly (Automated) .........................
Weekly, Quarterly (Non-automated)
Annual ..............................................
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PO 00000
Frm 00038
Number of
responses per
respondent
Number of
respondents
Form name
Fmt 4703
Sfmt 4703
Average
burden per
response
(in hr)
Total burden
(in hr)
50
10
50
50
50
52
52
52
1
1
20/60
2
4
75
12
867
1,040
10,400
3,750
600
5
5
5
5
5
52
56
52
1
1
20/60
20/60
4
5
12
87
93
1,040
25
60
3
3
3
52
56
1
20/60
20/60
5
52
56
15
E:\FR\FM\23OCN1.SGM
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Federal Register / Vol. 85, No. 206 / Friday, October 23, 2020 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS—Continued
Average
burden per
response
(in hr)
Total burden
(in hr)
Form name
Freely Associated States ..................
One-time Addition of Diseases and
Data Elements.
Weekly (Automated) .........................
Weekly (Non-automated) .................
Weekly (NMI Implementation) ..........
Annual ..............................................
One-time Addition of Diseases and
Data Elements.
3
1
12
36
2
2
2
2
2
52
52
52
1
1
20/60
2
4
75
12
35
208
416
150
24
...........................................................
........................
........................
........................
18,954
Cities
Cities
Cities
Cities
Cities
.................................................
.................................................
.................................................
.................................................
.................................................
Total ...........................................
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2020–23454 Filed 10–22–20; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier: CMS–R–148]
Agency Information Collection
Activities: Proposed Collection;
Comment Request
Centers for Medicare &
Medicaid Services, Health and Human
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 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
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
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 information to be
collected, and the use of automated
collection techniques or other forms of
information technology to minimize the
information collection burden.
SUMMARY:
khammond on DSKJM1Z7X2PROD with NOTICES
Number of
responses per
respondent
Number of
respondents
Type of respondent
VerDate Sep<11>2014
18:09 Oct 22, 2020
Jkt 253001
Comments must be received by
December 22, 2020.
DATES:
When commenting, please
reference the document identifier or
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 ___, 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’ website address at
https://www.cms.gov/Regulations-andGuidance/Legislation/Paperwork
ReductionActof1995/PRA-Listing.html.
2. Call the Reports Clearance Office at
(410) 786–1326.
ADDRESSES:
FOR FURTHER INFORMATION CONTACT:
William N. Parham at (410) 786–4669.
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).
PO 00000
Frm 00039
Fmt 4703
Sfmt 4703
CMS–R–148 Limitations on Provider
Related Donations and Health Care
Related Taxes, Medicaid and
Supporting Regulations in 42 CFR
433.68 Through 433.74
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.
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.
Information Collection
1. Type of Information Collection
Request: Extension of a currently
approved collection; Title of
Information Collection: Limitations on
Provider Related Donations and Health
Care Related Taxes, Medicaid and
Supporting Regulations in 42 CFR
433.68 through 433.74; Use: States may
elect to submit a waiver to CMS for the
broad based and/or uniformity
requirements for any health care related
tax program which does not conform to
the broad based and uniformity
requirements. It is also the
responsibility of each State to
demonstrate that their tax program(s) do
not violate the hold harmless provision.
For a waiver to be approved and a
determination that the hold harmless
provision is not violated, States must
submit written documentation which
satisfies the regulatory requirements.
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]]>Agencies
[Federal Register Volume 85, Number 206 (Friday, October 23, 2020)]
[Notices]
[Pages 67544-67546]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-23454]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-21-0728; Docket No. CDC-2020-0096]
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 the opportunity to comment on a proposed and/or
continuing information collection, as required by the Paperwork
Reduction Act of 1995. This notice invites comment on a proposed
information collection project titled National Notifiable Diseases
Surveillance System--Revision--Center for Surveillance, Epidemiology
and Laboratory Services (CSELS), Centers for Disease Control and
Prevention (CDC). The purpose of this data collection is to provide the
official source of statistics in the United States for nationally
notifiable conditions. Data will be used to monitor the occurrence and
spread of nationally notifiable conditions. Data will be gathered
through electronic submissions of case notifications to CDC from public
health departments from 50 states, New York City, Washington DC, five
U.S. territories, and three freely associated states.
DATES: CDC must receive written comments on or before December 22,
2020.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2020-
0096 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-D74, Atlanta, Georgia 30329.
Instructions: All submissions received must include the agency name
and Docket Number. CDC will post, without change, all relevant comments
to Regulations.gov.
Please note: Submit all comments 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-D74, Atlanta, Georgia 30329; phone: 404-639-7118; 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 the 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; and
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.
5. Assess information collection costs.
Proposed Project
National Notifiable Diseases Surveillance System (OMB Control No.
0920-0728, Exp. 04/30/2023)--Revision--Center for Surveillance,
Epidemiology and Laboratory Services (CSELS), Centers for Disease
Control and Prevention (CDC).
Background and Brief Description
The Public Health Services Act (42 U.S.C. 241) authorizes CDC to
[[Page 67545]]
disseminate nationally notifiable condition information. The National
Notifiable Diseases Surveillance System (NNDSS) is based on data
collected at the state, territorial and local levels as a result of
legislation and regulations in those jurisdictions that require health
care providers, medical laboratories, and other entities to submit
health-related data on reportable conditions to public health
departments. These reportable conditions, which include infectious and
non-infectious diseases, vary by jurisdiction depending upon each
jurisdiction's health priorities and needs. Each year, the Council of
State and Territorial Epidemiologists (CSTE), supported by CDC,
determines which reportable conditions should be designated nationally
notifiable or under standardized surveillance.
CDC requests a three-year approval for a Revision for the NNDSS
(OMB Control No. 0920-0728, Expiration Date 04/30/2023). This Revision
includes requests for approval to: (1) Receive case notification data
for Multisystem Inflammatory Syndrome (MIS) associated with Coronavirus
Disease 2019 (COVID-19); (2) receive new disease-specific data elements
for Anthrax, Brucellosis, Campylobacteriosis, Cholera,
Cryptosporidiosis, Hansen's Disease, Leptospirosis, Melioidosis, MIS
associated with COVID-19, COVID-19, S. Paratyphi Infection, S. Typhi
Infection, Salmonellosis, STEC, Shigellosis, and Vibriosis; and (3)
Receive new vaccine-related data elements for all conditions.
The NNDSS currently facilitates the submission and aggregation of
case notification data voluntarily submitted to CDC from 60
jurisdictions: public health departments in every U.S. state, New York
City, Washington DC, five U.S. territories (American Samoa, the
Commonwealth of Northern Mariana Islands, Guam, Puerto Rico, and the
U.S. Virgin Islands), and three freely associated states (Federated
States of Micronesia, the Republic of the Marshall Islands, and the
Republic of Palau). This information is shared across jurisdictional
boundaries and both surveillance and prevention and control activities
are coordinated at regional and national levels.
Approximately 90% of case notifications are encrypted and submitted
to NNDSS electronically from already existing databases by automated
electronic messages. When automated transmission is not possible, case
notifications are faxed, emailed, uploaded to a secure network or
entered into a secure website. All case notifications that are faxed or
emailed are done so in the form of an aggregate weekly or annual
report, not individual cases. These different mechanisms used to send
case notifications to CDC vary by the jurisdiction and the disease or
condition. Jurisdictions remove most personally identifiable
information (PII) before data are submitted to CDC, but some data
elements (e.g., date of birth, date of diagnosis, county of residence)
could potentially be combined with other information to identify
individuals. Private information is not disclosed unless otherwise
compelled by law. All data are treated in a secure manner consistent
with the technical, administrative, and operational controls required
by the Federal Information Security Management Act of 2002 (FISMA) and
the 2010 National Institute of Standards and Technology (NIST)
Recommended Security Controls for Federal Information Systems and
Organizations. Weekly tables of nationally notifiable diseases are
available through CDC WONDER and data.cdc.gov. Annual summaries of
finalized nationally notifiable disease data are published on CDC
WONDER and data.cdc.gov and disease-specific data are published by
individual CDC programs.
The burden estimates include the number of hours that the public
health department uses to process and send case notification data from
their jurisdiction to CDC. Specifically, the burden estimates include
separate burden hours incurred for automated and non-automated
transmissions, separate weekly burden hours incurred for modernizing
surveillance systems as part of NNDSS Modernization Initiative (NMI)
implementation, separate burden hours incurred for annual data
reconciliation and submission, and separate one-time burden hours
incurred for the addition of new diseases and data elements. The burden
estimates for the one-time burden for reporting jurisdictions are for
the addition of case notification data for MIS associated with COVID-
19; disease-specific data elements for Anthrax, Brucellosis,
Campylobacteriosis, Cholera, Cryptosporidiosis, Hansen's Disease,
Leptospirosis, Melioidosis, MIS associated with COVID-19, COVID-19, S.
Paratyphi Infection, S. Typhi Infection, Salmonellosis, STEC,
Shigellosis, and Vibriosis; and vaccine data elements for all diseases.
The estimated annual burden for the 257 respondents is 18,954 hours.
The cost of the information collection is $830,400. The total burden
hours increased from 18,414 to 18,954 since the last revision because
there were more disease-specific data elements added in this revision
as compared to the last revision.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Type of respondent Form name Number of responses per per response Total burden
respondents respondent (in hr) (in hr)
----------------------------------------------------------------------------------------------------------------
States........................ Weekly 50 52 20/60 867
(Automated).
States........................ Weekly (Non- 10 52 2 1,040
automated).
States........................ Weekly (NMI 50 52 4 10,400
Implementation).
States........................ Annual.......... 50 1 75 3,750
States........................ One-time 50 1 12 600
Addition of
Diseases and
Data Elements.
Territories................... Weekly 5 52 20/60 87
(Automated).
Territories................... Weekly, 5 56 20/60 93
Quarterly (Non-
automated).
Territories................... Weekly (NMI 5 52 4 1,040
Implementation).
Territories................... Annual.......... 5 1 5 25
Territories................... One-time 5 1 12 60
Addition of
Diseases and
Data Elements.
Freely Associated States...... Weekly 3 52 20/60 52
(Automated).
Freely Associated States...... Weekly, 3 56 20/60 56
Quarterly (Non-
automated).
Freely Associated States...... Annual.......... 3 1 5 15
[[Page 67546]]
Freely Associated States...... One-time 3 1 12 36
Addition of
Diseases and
Data Elements.
Cities........................ Weekly 2 52 20/60 35
(Automated).
Cities........................ Weekly (Non- 2 52 2 208
automated).
Cities........................ Weekly (NMI 2 52 4 416
Implementation).
Cities........................ Annual.......... 2 1 75 150
Cities........................ One-time 2 1 12 24
Addition of
Diseases and
Data Elements.
---------------------------------------------------------------------------------
Total..................... ................ .............. .............. .............. 18,954
----------------------------------------------------------------------------------------------------------------
Jeffrey M. Zirger,
Lead, Information Collection Review Office, Office of Scientific
Integrity, Office of Science, Centers for Disease Control and
Prevention.
[FR Doc. 2020-23454 Filed 10-22-20; 8:45 am]
BILLING CODE 4163-18-P
