60 Day FRN

37880

Federal Register / Vol. 88, No. 111 / Friday, June 9, 2023 / Notices

IX. Paperwork Reduction Act
The information collection required
by this permit has been submitted to
OMB under the provisions of the
Paperwork Reduction Act, 44 U.S.C.
3501 et seq., in submission made for the
NPDES permit program and assigned
OMB control number 2040–0004
[(NPDES Discharge Monitoring Reports
(DMRs)].
Because this permit is very similar in
reporting and application requirements
and in discharges which are required to
be monitored as the previous Eastern
Gulf of Mexico OCS general permit
(GEG460000), the paperwork burdens
are expected to be nearly identical. The
only new requirement is entry of acute
5 ..............

Media .........................................

Federal Communications Commission.
Marlene Dortch,
Secretary.

Dated: June 2, 2023.
Denisse Diaz,
Acting Director, Water Division.
[FR Doc. 2023–12292 Filed 6–8–23; 8:45 am]

BILLING CODE 6712–01–P

DATES:

[60Day–23–1309; Docket No. CDC–2023–
0047]

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 continuing information collection, as
required by the Paperwork Reduction
Act of 1995. This notice invites
comment on a proposed information
collection project titled Enterprise
Laboratory Information Management
System (ELIMS). This data collection is
used by CDC to record specimen
metadata and patient data related to test
order requests submitted by external
partners (SPHLs, International

SUMMARY:

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[FR ID 147101]

Deletion of Item From June 8, 2023
Open Meeting
June 6, 2023.

The following item was adopted and
released by the Commission on June 5,
2023 and deleted from the list of items
scheduled for consideration at the
Thursday, June 8, 2023, Open Meeting.
The item was previously listed in the
Commission’s Sunshine Notice on
Thursday, June 1, 2023.

Title: Restricted Adjudicatory Matter.
Summary: The Commission will consider a restricted adjudicatory matter.

[FR Doc. 2023–12355 Filed 6–8–23; 8:45 am]

Centers for Disease Control and
Prevention

FEDERAL COMMUNICATIONS
COMMISSION

BILLING CODE 6560–50–P

organizations, Federal institutions,
hospitals, doctor’s offices, etc.) to the
CDC Infectious Diseases testing
laboratories.

DEPARTMENT OF HEALTH AND
HUMAN SERVICES

lotter on DSK11XQN23PROD with NOTICES1

WET tests results for well treatment,
completion and workover fluids
discharged separately than produced
wastewaters into the electronic system.
When it issued the previous OCS
general permit, EPA estimated it would
take an affected facility three hours to
prepare the request for coverage and 38
hours per year to prepare DMRs. It is
estimated that the time required to
prepare the request for coverage and
DMRs for the reissued permit will be
approximately the same.

CDC must receive written
comments on or before August 8, 2023.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2023–
0047 by either of the following methods:
• Federal eRulemaking Portal:
www.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. CDC will post, without
change, all relevant comments to
www.regulations.gov.
Please note: Submit all comments
through the Federal eRulemaking portal
(www.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;
Telephone: 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

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Fmt 4703

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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;
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.

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37881

Federal Register / Vol. 88, No. 111 / Friday, June 9, 2023 / Notices
Proposed Project
Enterprise Laboratory Information
Management System (ELIMS) (OMB
Control No. 0920–1309, Exp. 11/30/
2023)—Revision—National Center for
Emerging and Zoonotic Infectious
Diseases (NCEZID), Centers for Disease
Control and Prevention (CDC).
Background and Brief Description
The collection of specimen
information designated for testing by the
CDC occurs on a regular and recurring
basis (multiple times per day) using an
electronic PDF file called the CDC
Specimen Submission 50.34 Form or an
electronic XSLX file called the Global
File Accessioning Template. Hospitals,
doctor’s offices, medical clinics,
commercial testing labs, universities,
State public health laboratories, U.S.
Federal institutions, and foreign
institutions use the CDC Specimen
Submission Form 50.34 when
submitting a single specimen to CDC
Infectious Diseases laboratories for
testing. The CDC Specimen Submission
50.34 Form consists of over 200 data

entry fields (of which five are
mandatory fields that must be
completed by the submitter) that
captures information about the
specimen being sent to the CDC for
testing. The type of data captured on the
50.34 Form identifies the origin of the
specimen (human, animal, food,
environmental, medical device or
biologic), CDC test order name/code,
specimen information, patient
information (as applicable), animal
information (as applicable) information
about the submitting organization
requesting the testing, patient history (as
applicable), owner information and
animal history (as applicable), and
epidemiological information. The
collection of this type of data is
pertinent to ensuring a specimen’s
testing results are linked to the correct
patient and the final test reports are
delivered to the appropriate submitting
organization to aid in making proper
health-related decisions related to the
patient. Furthermore, the data provided
on this form may be used by the CDC
to identify sources of potential
outbreaks and other public-health

related events. When the form is filled
out, a user in the submitting
organization prints a hard copy of it that
will be included in the specimen’s
shipping package sent to the CDC. The
printed form has barcodes on it that
allow the CDC testing laboratory to scan
its data directly into ELIMS where the
specimen’s testing lifecycle is tracked
and managed.
Likewise, the Global File
Accessioning Template records the
same data as the 50.34 Form but
provides the capability to submit
information for a batch of specimens
(typically 50–1,000 specimens per
batch) to a specific CDC laboratory for
testing. The CDC testing laboratory
electronically uploads the Global File
Accessioning Template into ELIMS
where the batch of specimens are then
logged and are ready to be tracked
through their respective testing and
reporting workflow.
CDC requests OMB approval for an
estimated 2,153 annual burden hours.
There is no cost to respondents other
than their time for participation.

ESTIMATED ANNUALIZED BURDEN HOURS
Form name

Medical Scientists, Except Epidemiologists, State Public Health
Lab, Medical Assistant, Doctor’s
Office/Hospital.
Medical Assistant, Doctor’s Office/
Hospital.

CDC Specimen Submission 50.34
Form.

Total ...........................................

...........................................................

[FR Doc. 2023–12360 Filed 6–8–23; 8:45 am]
BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–23–1333; Docket No. CDC–2023–
0045]

Proposed Data Collection Submitted
for Public Comment and
Recommendations
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).

AGENCY:

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ACTION:

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15

11

20/60

55

........................

........................

........................

2,153

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 Feeding My Baby and Me: Infant
Feeding Practices Study III (FMB&M–
IFPS III). This study is designed to
understand the current state of mothers’
intentions, behaviors, feeding decisions,
and practices from pregnancy through
their child’s first two years of life.
DATES: CDC must receive written
comments on or before August 8, 2023.

Fmt 4703

Total burden
(in hours)

5/60

Notice with comment period.

Frm 00036

Average
burden per
response
(in hours)

12

SUMMARY:

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Number of
responses per
respondent

2,098

Global File Accessioning Template

Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Public Health Ethics and
Regulations, Office of Science, Centers for
Disease Control and Prevention.

lotter on DSK11XQN23PROD with NOTICES1

Number of
respondents

Type of respondents

Sfmt 4703

You may submit comments,
identified by Docket No. CDC–2023–
0045 by either of the following methods:
• Federal eRulemaking Portal:
www.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. CDC will post, without
change, all relevant comments to
www.regulations.gov.
Please note: Submit all comments
through the Federal eRulemaking portal
(www.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
ADDRESSES:

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