60 day FRN

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Federal Register / Vol. 85, No. 106 / Tuesday, June 2, 2020 / Notices
Abstract

Regulation under delegated authority,
May 27, 2020.
Ann Misback,
Secretary of the Board.
[FR Doc. 2020–11771 Filed 6–1–20; 8:45 am]
BILLING CODE P

FEDERAL TRADE COMMISSION
Agency Information Collection
Activities; Submission for OMB
Review; Comment Request; Extension
Federal Trade Commission.
ACTION: Notice.
AGENCY:

The Federal Trade
Commission (‘‘FTC’’ or ‘‘Commission’’)
requests that the Office of Management
and Budget (‘‘OMB’’) extend for an
additional three years the current
Paperwork Reduction Act (‘‘PRA’’)
clearance for information collection
requirements associated with its Funeral
Industry Practice Rule (‘‘Funeral Rule’’
or ‘‘Rule’’). That clearance expires on
June 30, 2020.
DATES: Comments must be filed by July
2, 2020.
ADDRESSES: Written comments and
recommendations for the proposed
information collection should be sent
within 30 days of publication of this
notice to www.reginfo.gov/public/do/
PRAMain. Find this particular
information collection by selecting
‘‘Currently under Review—Open for
Public Comments’’ or by using the
search function.
FOR FURTHER INFORMATION CONTACT:
Patricia H. Poss, Division of Marketing
Practices, Bureau of Consumer
Protection, Federal Trade Commission,
600 Pennsylvania Ave. NW,
Washington, DC 20580, [email protected],
(202) 326–2413.
SUPPLEMENTARY INFORMATION: Pursuant
to the Paperwork Reduction Act of 1995
(44 U.S.C. 3501 et seq.), the FTC has
submitted to the Office of Management
and Budget (‘‘OMB’’) this request for
extension of the previously approved
collection of information discussed
below.
Title of Collection: Funeral Industry
Practice Rule, 16 CFR 453.
OMB Control Number: 3084–0025.
Type of Review: Extension without
change of currently approved collection.
Affected Public: Private Sector:
Businesses and other for-profit entities.
Estimated Number of Annual
Respondents: 19,136.
Estimated Annual Burden Hours:
164,006.
Estimated Annual Labor Costs:
$5,429,859.

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SUMMARY:

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The Funeral Rule ensures that
consumers who are purchasing funeral
goods and services have access to
accurate itemized price information so
they can purchase only the funeral
goods and services they want or need.
Among other things, the Rule requires a
funeral provider to: (1) Provide
consumers a copy of the funeral
provider’s General Price List that
itemizes the goods and services it offers;
(2) show consumers a Casket Price List
and an Outer Burial Container Price List
at the outset of any discussion of those
items or their prices, and in any event
before showing consumers caskets or
vaults; (3) provide price information
from its price lists over the telephone;
and (4) give consumers a Statement of
Funeral Goods and Services Selected
after determining the funeral
arrangements with consumers. The Rule
requires that funeral providers disclose
this information to consumers and
maintain records documenting their
compliance with the Rule.
Request for Comment
On February 4, 2020, the FTC sought
public comment on the information
collection requirements in the Funeral
Rule. 85 FR 6185 (Feb. 4, 2020). No
relevant comments were received.
Pursuant to the OMB regulations, 5 CFR
part 1320, the FTC is providing this
second opportunity for public comment
while seeking OMB approval to renew
clearance for the Rule’s information
collection requirements.
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, like 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, like medical records or
other individually identifiable health
information. In addition, do not include
any ‘‘[t]rade secret or any commercial or
financial information which is . . .
privileged or confidential’’ as provided
in Section 6(f) of the FTC Act 15 U.S.C.
46(f), and FTC Rule 4.10(a)(2), 16CFR
4.10(a)(2). In particular, do not include
competitively sensitive information
such as costs, sales statistics,
inventories, formulas, patterns devices,

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manufacturing processes, or customer
names.
Josephine Liu,
Assistant General Counsel for Legal Counsel.
[FR Doc. 2020–11877 Filed 6–1–20; 8:45 am]
BILLING CODE 6750–01–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–20–1204; Docket No. CDC–2020–
0053]

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 efforts 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 the ‘‘Behavioral Risk Factor
Surveillance System (BRFSS) Asthma
Call-back Survey (ACBS)’’ (OMB
Control No. 0920–1204, expiration date
11/30/2020). The ACBS is an in-depth
asthma survey conducted on a subset of
BRFSS respondents with an asthma
diagnosis. The goal of this survey is to
strengthen the existing body of asthma
data and to address critical questions
surrounding the health and experiences
of persons with asthma.
DATES: Written comments must be
received on or before August 3, 2020.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2020–
0053 by any of the following methods:
• Federal eRulemaking Portal:
Regulation.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.
SUMMARY:

Please note: Submit all comments through
the Federal eRulemaking portal

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Federal Register / Vol. 85, No. 106 / Tuesday, June 2, 2020 / Notices
(regulations.gov) or by U.S. mail to the
address listed above.
FOR FURTHER INFORMATION CONTACT:

Proposed Project
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].
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;

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SUPPLEMENTARY INFORMATION:

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.

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Behavioral Risk Factor Surveillance
System (BRFSS) Asthma Call-back
Survey (ACBS)—Revision—National
Center for Environmental Health
(NCEH), Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
The CDC’s National Center for
Environmental Health (NCEH) is
requesting a three-year Paperwork
Reduction Act (PRA) clearance to revise
and continue to collect information
under the ‘‘Behavioral Risk Factor
Surveillance System (BRFSS) Asthma
Call-back Survey (ACBS)’’ (OMB
Control No. 0920–1204, expiration date
11/30/2020). The ACBS is funded by the
NCEH National Asthma Control
Program (NACP) in the Asthma and
Community Health Branch (ACHB). The
NACP provides its 40 participating
states with technical and
methodological assistance.
The ACBS is a follow-up survey on
asthma and is administered on behalf of
NCEH by the CDC’s National Center for
Chronic Disease Prevention and Health
Promotion (NCCDPHP) BRFSS Program.
The BRFSS (OMB Control No. 0920–
1061, expiration date 3/31/2021) is a
nationwide system of customized, crosssectional telephone health surveys. The
BRFSS information collection is
conducted in a continuous, three-part
telephone interview process: screening,
participation in a common BRFSS core
survey, and participation in optional
question modules that states use to
customize survey content. BRFSS
coordinators in the health departments
in U.S. states, territories, and the
District of Columbia (collectively
referred to as ‘‘states’’ and
‘‘jurisdictions’’) are responsible for both
the BRFSS and the ACBS
administration. The ACBS is conducted
within two days after the BRFSS survey.
The purpose of ACBS is to gather
state-level asthma data and to make
them available to track the burden of the
disease, to monitor adherence to asthma
guidelines, and to direct and evaluate
interventions undertaken by asthma
control programs located in state health
departments. Beyond asthma prevalence
estimates, for most states, the ACBS
provides the only sources of adult and
child asthma data on the state and local
level.

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Data collection for ACBS involves
screening, obtaining permission,
consenting, and telephone interviewing
on a subset of the BRFSS respondents
from participating states. The ACBS
eligible respondents are BRFSS adults,
18 years and older, who report ever
being diagnosed with asthma. In
addition, some states include children,
below 18 years of age, who are
randomly selected subjects in the
BRFSS household. Parents or guardians
serve as ACBS proxy respondents for
their children ever diagnosed with
asthma. If both the BRFSS adult
respondent and the selected child in the
household have asthma, then only one
or the other is eligible for the ACBS.
State BRFSS Coordinators submit deidentified data files to CDC on a
monthly or quarterly basis for cleaning
and weighting. The CDC BRFSS ACBS
operation team returns clean, weighted
data files to the state of origin for its use.
The ACBS adds considerable state-level
depth to the existing body of asthma
data. It addresses critical questions
surrounding the health and experiences
of persons with asthma. Health data
include symptoms, environmental
factors, and medication use among
persons with asthma. Data on their
experiences include activity limitation,
health system use, and self-management
education. These asthma data are
needed to direct and evaluate
interventions undertaken by asthma
control programs located in state health
departments. Federal agencies and other
entities also rely on this critical
information for planning and evaluating
efforts and to reduce the burden from
this disease. The CDC makes annual
ACBS datasets available for public use
and provides guidance on statistically
appropriate uses of the data.
The time burden estimates are based
on the 2016 ACBS data collection,
which is the most recent data released.
The burden table reflects the landline
and cell phone data collection methods
used in 2016 and later years.
Additionally, the time burden accounts
for reporting burden incurred by the
states for the monthly or quarterly adult
and child ACBS data submissions to
CDC. The total estimated annualized
time burden for all respondents is 6,615
hours. Participation in the ACBS is
voluntary and there are no costs to
respondents other than their time.

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33672

Federal Register / Vol. 85, No. 106 / Tuesday, June 2, 2020 / Notices
ESTIMATED ANNUALIZED BURDEN TO RESPONDENTS
Average
burden per
response
(in hrs.)

Total burden
hours

Form name

BRFSS Adults ...................................

ACBS Landline Screener—Adult .....
ACBS Cell Phone Screener—Adult
ACBS Landline Screener—Child .....

17,800
16,733
2,576

1
1
1

1/60
1/60
1/60

297
279
43

ACBS Cell Phone Screener—Child
ACBS Adult Consent and Questionnaire.
ACBS Child Consent and Questionnaire.
ACBS Adult Data Submission Layout.
ACBS Child Data Submission Layout.

3,824
23,166

1
1

1/60
10/60

64
3,861

3,787

1

10/60

631

40

12

155/60

1,240

40

12

25/60

200

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

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

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

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

6,615

BRFSS Parents or Guardians of
Children.
ACBS Adults .....................................
ACBS Parents or Guardians of Children.
State BRFSS Coordinators ...............

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

Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2020–11803 Filed 6–1–20; 8:45 am]
BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–20–1027]

Agency Forms Undergoing Paperwork
Reduction Act Review

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Number of
responses per
respondent

Number of
respondents

Type of respondents

In accordance with the Paperwork
Reduction Act of 1995, the Centers for
Disease Control and Prevention (CDC)
has submitted the information
collection request titled ‘‘Generic
Clearance for the Collection of
Qualitative Feedback on Agency Service
Delivery’’ to the Office of Management
and Budget (OMB) for review and
approval. CDC previously published a
‘‘Proposed Data Collection Submitted
for Public Comment and
Recommendations’’ notice on March 9,
2020 to obtain comments from the
public and affected agencies. CDC
received one comment related to the
previous notice. This notice serves to
allow an additional 30 days for public
and affected agency comments.
CDC will accept all comments for this
proposed information collection project.
The Office of Management and Budget
is particularly interested in comments
that:
(a) Evaluate whether the proposed
collection of information is necessary
for the proper performance of the
functions of the agency, including

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whether the information will have
practical utility;
(b) Evaluate the accuracy of the
agencies estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used;
(c) Enhance the quality, utility, and
clarity of the information to be
collected;
(d) 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 submission of
responses; and
(e) Assess information collection
costs.
To request additional information on
the proposed project or to obtain a copy
of the information collection plan and
instruments, call (404) 639–7570.
Comments and recommendations for the
proposed information collection should
be sent within 30 days of publication of
this notice to www.reginfo.gov/public/
do/PRAMain. Find this particular
information collection by selecting
‘‘Currently under 30-day Review—Open
for Public Comments’’ or by using the
search function. Direct written
comments and/or suggestions regarding
the items contained in this notice to the
Attention: CDC Desk Officer, Office of
Management and Budget, 725 17th
Street NW, Washington, DC 20503 or by
fax to (202) 395–5806. Provide written
comments within 30 days of notice
publication.
Proposed Project
Generic Clearance for the Collection
of Qualitative Feedback on Agency
Service Delivery (OMB Control No.

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0920–1027, Exp. 7/31/2020)—
Extension—National Center for HIV/
AIDS, Viral Hepatitis, STD, and TB
Prevention (NCHHSTP), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
CDC is requesting a three-year
extension of this generic information
collection request. During the past
three-year approval period, the generic
clearance facilitated the approval of
seven projects (‘‘GenICs’’) involving
13,574 respondents. The projects
included web-based surveys, focus
groups, and assessments. The
information collection activities
conducted under this extension will
continue to garner qualitative customer
and stakeholder feedback in an efficient,
timely manner, in accordance with the
Administration’s commitment to
improving service delivery. By
qualitative feedback, we mean
information that provides useful
insights on perceptions and opinions,
but are not statistical surveys that yield
quantitative results that can be
generalized to the population of study.
This feedback will provide insights into
customer or stakeholder perceptions,
experiences and expectations, provide
an early warning of issues with service,
or focus attention on areas where
communication, training, or changes in
operations might improve delivery of
products or services. These collections
will allow for ongoing, collaborative,
and actionable communications
between the Agency and its customers
and stakeholders. It will also allow
feedback to contribute directly to the
improvement of program management.
Feedback collected under this generic
clearance will provide useful
information, but it will not yield data

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