Proposed Data Collection Submitted for Public Comment and Recommendations, 53501-53503 [2017-24804]
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Federal Register / Vol. 82, No. 220 / Thursday, November 16, 2017 / Notices
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[FR Doc. 2017–24871 Filed 11–15–17; 8:45 am]
BILLING CODE 4163–19–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–17–17BAN; Docket No. CDC–2017–
0081]
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 and/or
continuing information collections, as
required by the Paperwork Reduction
Act of 1995. This notice invites
comment on ‘‘Strengthening United
States Response to Resistant Gonorrhea
(SURRG).’’ The goal of the study is to
strengthen the U.S response to resistant
asabaliauskas on DSKBBXCHB2PROD with NOTICES
SUMMARY:
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gonorrhea by enhancing state and local
public health surveillance and program
infrastructure, build capacity to support
rapid detection and public health
response to antibiotic-resistant
gonorrhea, and advance the
understanding of epidemiological
factors contributing to antibioticresistant gonorrhea.
DATES: Written comments must be
received on or before January 16, 2018.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2017–
0081 by any of the following methods:
• Federal eRulemaking Portal:
Regulations.gov. Follow the instructions
for submitting comments.
• Mail: Leroy A. Richardson,
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 Leroy A.
Richardson, 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: 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
PO 00000
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53501
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
Strengthening U.S. Response to
Resistant Gonorrhea (SURRG)—New—
National Center for HIV/AIDS, Viral
Hepatitis, STD, and TB Prevention
(NCHHSTP), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
The purposes of Strengthening U.S.
Response to Resistant Gonorrhea
(SURRG) are to: (1) Improve national
capacity to detect, monitor, and respond
to emerging antibiotic-resistant
gonorrhea; (2) understand trends in and
factors contributing to antibioticresistant gonorrhea; and (3) build a
robust evidence base for public health
action. This information collection is
important because: (1) Effective
treatment of gonorrhea is critical to
gonorrhea control and prevention; (2)
untreated or inadequately treated
gonorrhea can cause serious
reproductive health complications, such
as infertility; (3) Neisseria gonorrhoeae
(the bacterium that causes gonorrhea)
has consistently demonstrated the
ability to develop resistance to the
antibiotics used for treatment and may
be developing resistance to the last
remaining treatment option
recommended by the CDC; and (4)
antibiotic-resistant gonorrhea is
extremely difficult to detect without
enhanced surveillance and public
health activities, such as SURRG,
because healthcare providers rarely
perform or have access to resistance
testing for individual patients.
SURRG will support rapid detection
of resistant gonorrhea and get actionable
information into the hands of healthcare
providers (to support appropriate
treatment of individual patients) and
local health departments (to support
rapid public health response to slow the
spread of resistant infections).
E:\FR\FM\16NON1.SGM
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53502
Federal Register / Vol. 82, No. 220 / Thursday, November 16, 2017 / Notices
Jurisdictions participating in SURRG
applied as part of a competitive process
and will participate voluntarily. As an
overview of SURRG, healthcare
providers at participating clinics
(sexually transmitted disease [STD]
clinics affiliated with a single public
health department or other participating
non-STD clinic sites) will collect
specimens for N. gonorrhoeae culture
testing from men and women seeking
care for possible gonorrhea. Specimens
that demonstrate N. gonorrhoeae (called
‘‘isolates’’) will undergo antibiotic
resistance testing within several days at
the local public health laboratory.
Laboratory results demonstrating
resistance be rapidly communicated by
the laboratory to the healthcare provider
and designated health department staff
member, who will initiate a field
investigation.
Researchers will interview the patient
(from whom the resistant specimen was
collected) about risk factors and recent
contacts, and will re-test to ensure cure.
The health department will interview
recent contacts and test them for
gonorrhea. The participating health
departments will collect and transmit to
CDC, demographic and clinical data
about persons tested for and diagnosed
with gonorrhea in the participating
clinics, results of local antibiotic
resistance testing, and information
about field investigations.
None of the data transmitted to CDC
will contain any personally identifiable
information. CDC will use the data to
monitor resistance, understand risk
factors for resistance, and identify new
approaches to prevent the spread of
resistance. CDC will receive transmitted
data through its Secure Access
Management Services (SAMS).
SURRG funded jurisdictions will
conduct antibiotic resistance testing on
all N. gonorrhoeae isolates from all STD
clinic sites and non-STD clinic sites
participating in SURRG. Each test takes
approximately 10 minutes of staff time,
and testing of control strains will also be
conducted approximately twice per
week at each laboratory. On average,
each jurisdiction will conduct
approximately 600 resistance tests per
year for patient care, plus 100 control
strains per year for quality assurance.
Thus, each grantee will perform
approximately 700 tests per year. Every
two months, a laboratory data manager
will abstract test results and securely
send the data file to the local SURRG
data manager. We estimate that
laboratory data managers will spend
approximately one hour each time they
abstract, clean, and transmit project
data.
Health department staff will interview
any person diagnosed with antibioticresistant gonorrhea or have a case of
gonorrhea of public health significance
index case, a diagnosed person’s social
and sexual contacts, and the sexual
contacts of the index case’s sexual
contacts.
On average, each jurisdiction will
identify four drug-resistant isolates each
month. These isolates will spur field
investigations, which will result in six
additional interviews each month. We
estimate 120 interviews will occur
annually at each site (annual 1,080
interviews for the 9 sites). Each
interview will take 30 minutes.
The total estimated annual burden
hours are 2,976. Respondents receive
federal funds to participate in this
project. There are no additional costs to
respondents other than their time.
SAMS is an approved federal
information technology system that
provides authorized and validated users
secure and encrypted access to CDC file
transfer applications. The encrypted
data will be stored in a secure CDC
server with strictly controlled and
restricted access rights.
Researchers will ship isolates each
month to one of four Antibiotic
Resistance Regional Laboratory Network
(ARLN) laboratories for confirmatory
antibiotic susceptibility testing and
molecular characterization.
Under the SURRG protocol, the local
SURRG data managers from each of the
funded jurisdictions will abstract STD
clinic data for patients tested for
gonorrhea, receive data from non-STD
clinic healthcare sites about persons
tested for gonorrhea, receive resistance
testing laboratory results from local
public health laboratories, abstract data
about field investigations, and will
merge the data. Every two months, the
local SURRG data manager will clean
the data, remove personally identifiable
information, and transmit the data to
CDC. We estimate these data processes
will take 16 hours every two months.
Annually, the local SURRG data
manager will send a final cumulative
data file. Seven data transmissions/
responses will occur.
Every two months, data managers at
each of the participating non-STD clinic
health centers will abstract and clean
data and securely transmit the data to
the local SURRG data manager. We
estimate that it will take three hours
each time data managers at each nonSTD SURRG location abstract, clean,
and transmit SURRG data.
Microbiologists at public health
laboratories from each of the nine
ESTIMATE OF ANNUALIZED BURDEN HOURS
Average
burden per
response
(hours)
Number of
responses per
respondent
Form name
Local SURRG data manager ............
asabaliauskas on DSKBBXCHB2PROD with NOTICES
Type of
respondent
Facility, Laboratory and field Elements.
Non-STD clinic Elements .................
9
7
16
1,008
18
6
3
324
Laboratory Testing ...........................
9
700
10/60
1,050
Laboratory Elements ........................
9
6
1
54
Field Investigation Elements ............
1,080
1
30/60
540
..........................................................
........................
........................
........................
2,976
Data manager at non-STD clinic
health centers.
Public Health Laboratory Microbiologist.
Public Health Laboratory Data Manager.
Gonorrhea Patients, Social and Sexual Contacts.
Total ...........................................
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Number of
respondents
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Total burden
hours
Federal Register / Vol. 82, No. 220 / Thursday, November 16, 2017 / 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. 2017–24804 Filed 11–15–17; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier: CMS–10237]
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 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:
Comments on the collection(s) of
information must be received by the
OMB desk officer by December 18, 2017.
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.
asabaliauskas on DSKBBXCHB2PROD with NOTICES
DATES:
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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
Web site address at https://
www.cms.gov/Regulations-andGuidance/Legislation/Paperwork
ReductionActof1995/PRA-Listing.html.
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:
William Parham at (410) 786–4669.
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
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: Applications for
Part C Medicare Advantage, 1876 Cost
Plans, and Employer Group Waiver
Plans to Provide Part C Benefits; Use:
This information collection includes the
process for organizations wishing to
provide healthcare services under MA
and/or MA–PD plans must complete an
application annually, file a bid, and
receive final approval from CMS. The
application process has two options for
applicants that include: Request for new
MA product or request for expanding
the service area of an existing product.
This collection process is the only
mechanism for MA and/or MA–PD
organizations to complete the required
application process. CMS utilizes the
application process as the means to
review, assess and determine if
applicants are compliant with the
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53503
current requirements for participation in
the Medicare Advantage program and to
make a decision related to contract
award. Form Number: CMS–10237
(OMB control number: 0938–0935);
Frequency: Yearly; Affected Public:
Private sector (Business or other Forprofits and Not-for-profit institutions);
Number of Respondents: 380; Total
Annual Responses: 380; Total Annual
Hours: 6,246. (For policy questions
regarding this collection contact Stacy
Davis at 410–786–7813.)
Dated: November 13, 2017.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office
of Strategic Operations and Regulatory
Affairs.
[FR Doc. 2017–24816 Filed 11–15–17; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifiers: CMS–10401]
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 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:
Comments on the collection(s) of
information must be received by the
OMB desk officer by December 18, 2017.
DATES:
E:\FR\FM\16NON1.SGM
16NON1
]]>Agencies
[Federal Register Volume 82, Number 220 (Thursday, November 16, 2017)]
[Notices]
[Pages 53501-53503]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2017-24804]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-17-17BAN; Docket No. CDC-2017-0081]
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 and/or
continuing information collections, as required by the Paperwork
Reduction Act of 1995. This notice invites comment on ``Strengthening
United States Response to Resistant Gonorrhea (SURRG).'' The goal of
the study is to strengthen the U.S response to resistant gonorrhea by
enhancing state and local public health surveillance and program
infrastructure, build capacity to support rapid detection and public
health response to antibiotic-resistant gonorrhea, and advance the
understanding of epidemiological factors contributing to antibiotic-
resistant gonorrhea.
DATES: Written comments must be received on or before January 16, 2018.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2017-
0081 by any of the following methods:
Federal eRulemaking Portal: Regulations.gov. Follow the
instructions for submitting comments.
Mail: Leroy A. Richardson, 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 Leroy A. Richardson, 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: 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
Strengthening U.S. Response to Resistant Gonorrhea (SURRG)--New--
National Center for HIV/AIDS, Viral Hepatitis, STD, and TB Prevention
(NCHHSTP), Centers for Disease Control and Prevention (CDC).
Background and Brief Description
The purposes of Strengthening U.S. Response to Resistant Gonorrhea
(SURRG) are to: (1) Improve national capacity to detect, monitor, and
respond to emerging antibiotic-resistant gonorrhea; (2) understand
trends in and factors contributing to antibiotic-resistant gonorrhea;
and (3) build a robust evidence base for public health action. This
information collection is important because: (1) Effective treatment of
gonorrhea is critical to gonorrhea control and prevention; (2)
untreated or inadequately treated gonorrhea can cause serious
reproductive health complications, such as infertility; (3) Neisseria
gonorrhoeae (the bacterium that causes gonorrhea) has consistently
demonstrated the ability to develop resistance to the antibiotics used
for treatment and may be developing resistance to the last remaining
treatment option recommended by the CDC; and (4) antibiotic-resistant
gonorrhea is extremely difficult to detect without enhanced
surveillance and public health activities, such as SURRG, because
healthcare providers rarely perform or have access to resistance
testing for individual patients.
SURRG will support rapid detection of resistant gonorrhea and get
actionable information into the hands of healthcare providers (to
support appropriate treatment of individual patients) and local health
departments (to support rapid public health response to slow the spread
of resistant infections).
[[Page 53502]]
Jurisdictions participating in SURRG applied as part of a
competitive process and will participate voluntarily. As an overview of
SURRG, healthcare providers at participating clinics (sexually
transmitted disease [STD] clinics affiliated with a single public
health department or other participating non-STD clinic sites) will
collect specimens for N. gonorrhoeae culture testing from men and women
seeking care for possible gonorrhea. Specimens that demonstrate N.
gonorrhoeae (called ``isolates'') will undergo antibiotic resistance
testing within several days at the local public health laboratory.
Laboratory results demonstrating resistance be rapidly communicated by
the laboratory to the healthcare provider and designated health
department staff member, who will initiate a field investigation.
Researchers will interview the patient (from whom the resistant
specimen was collected) about risk factors and recent contacts, and
will re-test to ensure cure. The health department will interview
recent contacts and test them for gonorrhea. The participating health
departments will collect and transmit to CDC, demographic and clinical
data about persons tested for and diagnosed with gonorrhea in the
participating clinics, results of local antibiotic resistance testing,
and information about field investigations.
None of the data transmitted to CDC will contain any personally
identifiable information. CDC will use the data to monitor resistance,
understand risk factors for resistance, and identify new approaches to
prevent the spread of resistance. CDC will receive transmitted data
through its Secure Access Management Services (SAMS).
SAMS is an approved federal information technology system that
provides authorized and validated users secure and encrypted access to
CDC file transfer applications. The encrypted data will be stored in a
secure CDC server with strictly controlled and restricted access
rights.
Researchers will ship isolates each month to one of four Antibiotic
Resistance Regional Laboratory Network (ARLN) laboratories for
confirmatory antibiotic susceptibility testing and molecular
characterization.
Under the SURRG protocol, the local SURRG data managers from each
of the funded jurisdictions will abstract STD clinic data for patients
tested for gonorrhea, receive data from non-STD clinic healthcare sites
about persons tested for gonorrhea, receive resistance testing
laboratory results from local public health laboratories, abstract data
about field investigations, and will merge the data. Every two months,
the local SURRG data manager will clean the data, remove personally
identifiable information, and transmit the data to CDC. We estimate
these data processes will take 16 hours every two months. Annually, the
local SURRG data manager will send a final cumulative data file. Seven
data transmissions/responses will occur.
Every two months, data managers at each of the participating non-
STD clinic health centers will abstract and clean data and securely
transmit the data to the local SURRG data manager. We estimate that it
will take three hours each time data managers at each non-STD SURRG
location abstract, clean, and transmit SURRG data.
Microbiologists at public health laboratories from each of the nine
SURRG funded jurisdictions will conduct antibiotic resistance testing
on all N. gonorrhoeae isolates from all STD clinic sites and non-STD
clinic sites participating in SURRG. Each test takes approximately 10
minutes of staff time, and testing of control strains will also be
conducted approximately twice per week at each laboratory. On average,
each jurisdiction will conduct approximately 600 resistance tests per
year for patient care, plus 100 control strains per year for quality
assurance. Thus, each grantee will perform approximately 700 tests per
year. Every two months, a laboratory data manager will abstract test
results and securely send the data file to the local SURRG data
manager. We estimate that laboratory data managers will spend
approximately one hour each time they abstract, clean, and transmit
project data.
Health department staff will interview any person diagnosed with
antibiotic-resistant gonorrhea or have a case of gonorrhea of public
health significance index case, a diagnosed person's social and sexual
contacts, and the sexual contacts of the index case's sexual contacts.
On average, each jurisdiction will identify four drug-resistant
isolates each month. These isolates will spur field investigations,
which will result in six additional interviews each month. We estimate
120 interviews will occur annually at each site (annual 1,080
interviews for the 9 sites). Each interview will take 30 minutes.
The total estimated annual burden hours are 2,976. Respondents
receive federal funds to participate in this project. There are no
additional costs to respondents other than their time.
Estimate of Annualized Burden Hours
--------------------------------------------------------------------------------------------------------------------------------------------------------
Average
Number of Number of burden per Total burden
Type of respondent Form name respondents responses per response hours
respondent (hours)
--------------------------------------------------------------------------------------------------------------------------------------------------------
Local SURRG data manager....................... Facility, Laboratory and field Elements 9 7 16 1,008
Data manager at non-STD clinic health centers.. Non-STD clinic Elements................ 18 6 3 324
Public Health Laboratory Microbiologist........ Laboratory Testing..................... 9 700 10/60 1,050
Public Health Laboratory Data Manager.......... Laboratory Elements.................... 9 6 1 54
Gonorrhea Patients, Social and Sexual Contacts. Field Investigation Elements........... 1,080 1 30/60 540
---------------------------------------------------------------
Total...................................... ....................................... .............. .............. .............. 2,976
--------------------------------------------------------------------------------------------------------------------------------------------------------
[[Page 53503]]
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. 2017-24804 Filed 11-15-17; 8:45 am]
BILLING CODE 4163-18-P
