60-day Federal Register Notice

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ESTIMATED ANNUALIZED BURDEN HOURS—Continued

Total burden
(in hours)

Form name

Epidemiologist ........

Attachment G—U.S. Outpatient Influenza-like Illness
Surveillance Network (ILINet) Weekly—CDC 55.20.
Attachment H—U.S. Outpatient Influenza-like Illness
Surveillance Network (ILINet) Workfolder 55.20E.
Attachment J—Influenza-Associated Pediatric Mortality—Case Report Form.
Attachment K—Human Infection with Novel Influenza
A Virus Case Report Form.
Attachment M—Human Infection with Novel Influenza A Virus Severe Outcomes.
Attachment P—Novel Influenza A Virus Case
Screening Form.
Attachment T—Antiviral Resistant Influenza Infection
Case Report Form.
Attachment U—National Respiratory & Enteric Virus
Surveillance System (NREVSS) (55.83A, B, D)
(electronic).
Attachment V—National Enterovirus Surveillance
Report: (CDC 55.9) (electronic).
Attachment W—National Adenovirus Type Reporting
System (NATRS).
Attachment X—Middle East Respiratory Syndrome
(MERS) Patient Under Investigation (PUI) Short
Form.
Attachment Y—Viral Gastroenteritis Outbreak Submission Form.
Attachment AA—Influenza Virus (Electronic, Year
Round), PHLIP_HL7 messaging Data Elements.
Attachment BB—Influenza virus (electronic, year
round) (PHIN–MS).
Attachment CC—Suspect Respiratory Virus Patient
Form.

1,800

52

10/60

15,600

1,800

1

5/60

150

57

2

30/60

57

57

2

30/60

57

57

1

90/60

86

57

1

15/60

14

57

3

30/60

86

550

52

15/60

7,150

20

12

15/60

60

13

4

15/60

13

57

3

25/60

71

20

5

5/60

8

57

52

5/60

247

3

52

5/60

13

10

5

30/60

25

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

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

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

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

24,115

Epidemiologist ........
Epidemiologist ........
Epidemiologist ........
Epidemiologist ........
Epidemiologist ........
Epidemiologist ........
Epidemiologist ........
Epidemiologist ........
Epidemiologist ........
Epidemiologist ........
Epidemiologist ........
Epidemiologist ........
Epidemiologist ........
Epidemiologist ........
Total ................

Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2020–06019 Filed 3–20–20; 8:45 am]
BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day-FY–2020; Docket No. CDC–2020–
0032]

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:

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Average
burden per
response
(in hours)

Number of
responses per
respondent

Number of
respondents

Type of respondents

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

SUMMARY:

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17:26 Mar 20, 2020

Jkt 250001

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 the Customer Surveys
Generic Clearance for the National
Center for Health Statistics. This
collection is used to assess NCHS
customers’ satisfaction with the content,
quality and relevance of the information
it produces.
DATES: Written comments must be
received on or before May 22, 2020.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2020–
0032 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. All relevant comments

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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–
D74, 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

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Federal Register / Vol. 85, No. 56 / Monday, March 23, 2020 / Notices
focus groups, automated and electronic
technology (e.g., email, Web-based
surveys), and telephone surveys.
Systematic surveys of several groups
will be folded into the program. Among
these are Federal customers and policy
makers, state and local officials who
rely on NCHS data, the broader
educational, research, and public health
community, and other data users.
Respondents may include data users
who register for and/or attend NCHS
sponsored conferences; persons who
access the NCHS website and the
detailed data available through it;
consultants; and others. Respondent
data items may include (in broad
categories) information regarding
respondent’s gender, age, occupation,
affiliation, location, etc., to be used to
characterize responses only. Other
questions will attempt to obtain
information that will characterize the
respondents’ familiarity with and use of
NCHS data, their assessment of data
content and usefulness, general
satisfaction with available services and
products, and suggestions for
improvement of surveys, services and
products.
In order to capture anticipated
feedback opportunities, this extension
request allows a total estimated annual
burden total of 4,000 hours. There is no
cost to respondents other than their time
to participate in the survey. The
resulting information will be for NCHS
internal use.

Proposed Project

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; 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.

Customer Surveys Generic Clearance
for the National Center for Health
Statistics (OMB Control No. 0920–0729,
Exp. 09/30/2020)—Extension—National
Center for Health Statistics (NCHS),
Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
Section 306 of the Public Health
Service (PHS) Act (42 U.S.C. 242k), as
amended, authorizes that the Secretary
of Health and Human Services (DHHS),
acting through NCHS, shall collect
statistics on ‘‘the extent and nature of
illness and disability of the population
of the United States.’’ This is an
extension request for a generic approval
from OMB to conduct customer surveys
over the next three years at an overall
burden rate of 4000 hours.
As part of a comprehensive program,
the National Center for Health Statistics
(NCHS) plans to continue to assess its
customers’ satisfaction with the content,
quality and relevance of the information
it produces. NCHS will conduct
voluntary customer surveys to assess
strengths in agency products and
services and to evaluate how well it
addresses the emerging needs of its data
users. Results of these surveys will be
used in future planning initiatives.
The data will be collected using a
combination of methodologies
appropriate to each survey. These may
include: evaluation forms, mail surveys,

ESTIMATED ANNUALIZED BURDEN HOURS
Type of respondents

Questionnaire for conference
registrants/attendees.
Focus groups .............................
Web-based .................................
Other customer surveys .............
Total ....................................

Number of
respondents

Form name

Public/private
and others.
Public/private
and others.
Public/private
and others.
Public/private
and others.

6,000

1

15/60

1,500

researchers, Consultants,

500

1

1

500

researchers, Consultants,

6,000

1

15/60

1,500

researchers, Consultants,

2,000

1

15/60

500

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

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

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

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

4,000

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration

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[FR Doc. 2020–06023 Filed 3–20–20; 8:45 am]

[Docket No. FDA–2020–N–0008]

BILLING CODE 4163–18–P

Blood Products Advisory Committee;
Postponed
AGENCY:

Food and Drug Administration,

HHS.

17:26 Mar 20, 2020

Total burden
(in hrs.)

researchers, Consultants,

Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.

VerDate Sep<11>2014

Average
burden per
response
(in hrs.)

Number of
responses per
respondent

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ACTION:

Notice.

The meeting of the Blood
Products Advisory Committee (BPAC)
scheduled for April 2–3, 2020, is
postponed. The Food and Drug
Administration (FDA), like other
government agencies, is taking the
necessary steps to ensure the Agency is
prepared to continue our vital public
health mission in the event that our dayto-day operations are impacted by the

SUMMARY:

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