Agency Information Collection Activities: Submission for OMB Review; Comment Request, 28948-28950 [2020-10282]
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jbell on DSKJLSW7X2PROD with NOTICES
28948
Federal Register / Vol. 85, No. 94 / Thursday, May 14, 2020 / Notices
public on service delivery, the Federal
Trade Commission (‘‘FTC’’ or
‘‘Commission’’) is submitting a Generic
Information Collection Request (Generic
ICR): ‘‘Generic Clearance for the
Collection of Qualitative Feedback on
Agency Service Delivery’’ to OMB for
approval under the Paperwork
Reduction Act.
DATES: Comments must be submitted by
June 15, 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 30-day Review—Open
for Public Comments’’ or by using the
search function.
FOR FURTHER INFORMATION CONTACT:
Bridget Small, Federal Trade
Commission, 600 Pennsylvania Avenue
NW, CC–10402, Washington, DC 20580,
(202) 326–3266.
SUPPLEMENTARY INFORMATION:
Title: Generic Clearance for the
Collection of Qualitative Feedback on
Agency Service Delivery.
Abstract: The information collection
activity will 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
that can be generalized to the overall
population. This type of generic
clearance for qualitative information
will not be used for quantitative
information collections that are
designed to yield reliably actionable
results, such as monitoring trends over
time or documenting program
performance. Such data uses require
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more rigorous designs that address: the
target population to which
generalizations will be made, the
sampling frame, the sample design
(including stratification and clustering),
the precision requirements or power
calculations that justify the proposed
sample size, the expected response rate,
methods for assessing potential nonresponse bias, the protocols for data
collection, and any testing procedures
that were or will be undertaken prior
fielding the study. Depending on the
degree of influence the results are likely
to have, such collections may still be
eligible for submission for other generic
mechanisms that are designed to yield
quantitative results.
Type of Review: Extension of a
currently approved collection.
Affected Public: Individuals and
Households, Businesses and
Organizations, State, Local or Tribal
Government.
Average Expected Annual Number of
Activities: 35.
Estimated Number of Annual
Respondents: 5,764.1
Frequency of Response: Once per
request.
Annual Responses: 5,764.
Average Minutes Per Response: 18
(rounded to nearest whole minute).
Estimated Total Annual Burden
Hours: 1,759.
An agency may not conduct or
sponsor, and a person is not required to
respond to, a collection of information
unless it displays a currently valid OMB
control number. The control number for
the existing clearance (expiring May 31,
2020) is 3084–0159. The FTC seeks
renewed three-year clearance under this
control number for the prospective
collection of information and the
associated burden estimates.
Request for Comment:
On December 26, 2019, the
Commission sought comment on the
renewal of this generic clearance. 84 FR
70972. One relevant comment was
received from an interested person. The
commenter stated that he believed the
collection and analysis of these
qualitative statistics will be useful in
improving the delivery of the many
services of the FTC.
1 Projected
activities: (1) Eleven customer
satisfaction surveys per year of 500 respondents
each (surveys to get feedback about major
campaigns, publications, websites, branding and
other consumer and business education products to
test their appeal and effectiveness), 0.25 hours (i.e.
15 minutes) per response; (2) Twelve focus groups
per year, 10 respondents each (to test education
products and websites), 2 hours per response; and
(3) Twelve usability sessions per year, 12
respondents per website (to test the usability of FTC
websites by inviting people to complete common
tasks on those sites), 1 hour per response.
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Pursuant to the OMB regulations, 5
CFR part 1320, that implement the PRA,
44 U.S.C. 3501 et seq., the FTC is
providing this second opportunity for
public comment while seeking OMB
approval to renew the pre-existing
clearance for those information
collection requirements. An agency may
not conduct or sponsor, and a person is
not required to respond to a collection
of information unless it displays a valid
OMB control number.
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,
manufacturing processes, or customer
names.
Josephine Liu,
Assistant General Counsel for Legal Counsel.
[FR Doc. 2020–10307 Filed 5–13–20; 8:45 am]
BILLING CODE 6750–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifiers CMS–10275, CMS–R–
64, and CMS–10710]
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
SUMMARY:
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14MYN1
jbell on DSKJLSW7X2PROD with NOTICES
Federal Register / Vol. 85, No. 94 / Thursday, May 14, 2020 / Notices
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.
DATES: Comments on the collection(s) of
information must be received by the
OMB desk officer by June 15, 2020.
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:
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 30-day Review—Open
for Public Comments’’ or by using the
search function.
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
website address at https://www.cms.gov/
Regulations-and-Guidance/Legislation/
PaperworkReductionActof1995/PRAListing.html.
1. Email your request, including your
address, phone number, OMB number,
and CMS document identifier, to
Paperwork@cms.hhs.gov.
2. 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
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18:29 May 13, 2020
Jkt 250001
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: Extension without change of a
currently approved collection; Title of
Information Collection: CAHPS Home
Health Care Survey; Use: The national
implementation of the Home Health
Care CAHPS Survey is designed to
collect ongoing data from samples of
home health care patients who receive
skilled services from Medicare-certified
home health agencies.
The survey is necessary because it
fulfills the goal of transparency with the
public about home health patient
experiences. The survey is used by
Medicare-certified home health agencies
to improve their internal quality
assurance in the care that they provide
in home health. The HHCAHPS survey
is also used in a Medicare payment
program. Medicare-certified home
health agencies (HHAs) must contract
with CMS-approved survey vendors that
conduct the HHCAHPS on behalf of the
HHAs to meet their requirements in the
Home Health Quality Reporting
Program. Form Number: CMS–10257
(OMB control number: 0938–1066);
Frequency: Yearly; Affected Public:
Individuals and Households; Number of
Respondents: 1,195,930; Total Annual
Responses: 1,294,820; Total Annual
Hours: 453,239. (For policy questions
regarding this collection contact Lori
Teichman at 410–786–6684.)
2. Type of Information Collection
Request: Extension without change of a
currently approved collection; Title of
Information Collection: Indirect Medical
Education and Direct Graduate Medical
Education; Use: Section 1886(d)(5)(B) of
the Social Security Act requires
additional payments to be made under
the Medicare Prospective Payment
System (PPS) for the indirect medical
educational costs a hospital incurs in
connection with interns and residents
(IRs) in approved teaching programs. In
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28949
addition, Title 42, Part 413, sections 75
through 83 implement section 1886(d)
of the Act by establishing the
methodology for Medicare payment for
the costs of direct graduate medical
educational activities. These payments,
which are adjustments (add-ons) to
other payments made to a hospital
under PPS, are largely determined by
the number of full-time equivalent (FTE)
IRs that work at a hospital during its
cost reporting period. In Federal fiscal
year (FY) 2018, the estimated Medicare
program payments for indirect medical
education (IME) costs was $6.4 billion.
Medicare program payment for direct
graduate medical education (GME) is
also based upon the number of FTE–IRs
that work at a hospital. In FY 2018, the
estimated Medicare program payments
for GME costs was $3.1 billion.
Since it is important to accurately
count the number of IRs FTEs working
at each hospital, original approval was
obtained from the Office of Management
and Budget (OMB) in 1985 to collect the
IR information required in 42 CFR
412.105(f) and timeframes for filing. All
Medicare health plans are required to
use these standardized notices. Form
Number: CMS–R–64 (OMB control
number: 0938–0456); Frequency: Yearly;
Affected Public: State, Local, or Tribal
Governments; Number of Respondents:
1,245; Total Annual Responses: 1,245;
Total Annual Hours: 2,490. (For policy
questions regarding this collection
contact Owen Osaghae at 410–786–
7550.)
3. Type of Information Collection
Request: New collection (Request for a
new OMB control number) collection;
Title of Information Collection: Generic
Clearance for Improving Customer
Experience (OMB Circular A–11,
Section 280 Implementation); Use:
Whether seeking a loan, Social Security
benefits, veterans benefits, or other
services provided by the Federal
Government, individuals and businesses
expect Government customer services to
be efficient and intuitive, just like
services from leading private-sector
organizations. Yet the 2016 American
Consumer Satisfaction Index and the
2017 Forrester Federal Customer
Experience Index show that, on average,
Government services lag nine
percentage points behind the private
sector.
A modern, streamlined and
responsive customer experience means:
Raising government-wide customer
experience to the average of the private
sector service industry; developing
indicators for high-impact Federal
programs to monitor progress towards
excellent customer experience and
mature digital services; and providing
E:\FR\FM\14MYN1.SGM
14MYN1
28950
Federal Register / Vol. 85, No. 94 / Thursday, May 14, 2020 / Notices
the structure (including increasing
transparency) and resources to ensure
customer experience is a focal point for
agency leadership. To support this,
OMB Circular A–11 Section 280
established government-wide standards
for mature customer experience
organizations in government and
measurement. To enable Federal
programs to deliver the experience
taxpayers deserve, they must undertake
three general categories of activities:
Conduct ongoing customer research,
gather and share customer feedback, and
test services and digital products.
These data collection efforts may be
either qualitative or quantitative in
nature or may consist of mixed
methods. Additionally, data may be
collected via a variety of means,
including but not limited to electronic
or social media, direct or indirect
observation (i.e., in person, video and
audio collections), interviews,
questionnaires, surveys, and focus
groups. The Centers for Medicare and
Medicaid Services (CMS) will limit its
inquiries to data collections that solicit
strictly voluntary opinions or responses.
Steps will be taken to ensure anonymity
of respondents in each activity covered
by this request.
The results of the data collected will
be used to improve the delivery of
Federal services and programs. It will
include the creation of personas,
customer journey maps, and reports and
summaries of customer feedback data
and user insights. It will also provide
government-wide data on customer
experience that can be displayed on
performance.gov to help build
transparency and accountability of
Federal programs to the customers they
serve.
Dated: May 8, 2020.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office
of Strategic Operations and Regulatory
Affairs.
[FR Doc. 2020–10282 Filed 5–13–20; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
ACTION:
Notice.
The Food and Drug
Administration (FDA or Agency) is
withdrawing approval of 16 new drug
applications (NDAs) from multiple
applicants. The applicants notified the
Agency in writing that the drug
products were no longer marketed and
requested that the approval of the
applications be withdrawn.
SUMMARY:
Approval is withdrawn as of
June 15, 2020.
DATES:
FOR FURTHER INFORMATION CONTACT:
Kimberly Lehrfeld, Center for Drug
Evaluation and Research, Food and
Drug Administration, 10903 New
Hampshire Ave., Bldg. 51, Rm. 6226,
Silver Spring, MD 20993–0002, 301–
796–3137.
The
applicants listed in the table have
informed FDA that these drug products
are no longer marketed and have
requested that FDA withdraw approval
of the applications under the process in
§ 314.150(c) (21 CFR 314.150(c)). The
applicants have also, by their requests,
waived their opportunity for a hearing.
Withdrawal of approval of an
application or abbreviated application
under § 314.150(c) is without prejudice
to refiling.
SUPPLEMENTARY INFORMATION:
Food and Drug Administration
[Docket No. FDA–2020–N–1117]
Janssen Pharmaceuticals, Inc., et al.;
Withdrawal of Approval of 16 New
Drug Applications
AGENCY:
Food and Drug Administration,
HHS.
Application No.
Drug
Applicant
NDA 011529 ..........
NDA 019579 ..........
Parafon Forte DSC (chlorzoxazone), Caplets, 500 milligrams (mg).
Ritalin-SR (methylphenidate hydrochloride (HCl)) ExtendedRelease Tablets, 20 mg.
Depakene (valproic acid) Oral Solution, 250 mg/5 milliliter
(mL).
Terazol 7 (terconazole) Vaginal Cream, 0.4% .......................
NDA 020119 ..........
Vumon (teniposide) Injection, 10 mg/mL ...............................
NDA 020388 ..........
NDA 020741 ..........
Navelbine (vinorelbine tartrate) Injection, Equivalent to (EQ)
10 mg/mL base.
Prandin (repaglinide) Tablets, 0.5 mg, 1.0 mg, and 2.0 mg ..
NDA 020920 ..........
Natrecor (nesiritide) Injection, 1.5 mg/vial .............................
NDA 021001 ..........
Axert (almotriptan malate) Tablets, EQ 6.25 mg base and
EQ 12.5 mg base.
Tricor (fenofibrate) Tablets, 54 mg and 160 mg ....................
Striant (testosterone buccal system) Extended-Release Tablets, 30 mg.
Children’s ElixSure IB (ibuprofen) Oral Suspension, 100mg/
5 mL.
Janssen Pharmaceuticals, Inc., 1000 Route 202 South, P.O.
Box 300, Raritan, NJ 08869.
Novartis Pharmaceuticals Corp., 1 Health Plaza, East Hanover, NJ 07936.
AbbVie Inc., 1 North Waukegan Rd., North Chicago, IL
60064.
Janssen Pharmaceuticals, Inc., 1125 Trenton-Harbourton
Rd., Titusville, NJ 08560.
HQ Specialty Pharma, 120 Route 17 North, Paramus, NJ
07652.
Pierre Fabre Medicament c/o Pierre Fabre Pharmaceuticals,
Inc., 8 Campus Dr., Suite 202, Parsippany, NJ 07054.
Gemini Laboratories, LLC, 400 Crossing Blvd., 5th Floor,
Bridgewater, NJ 08807.
Scios, LLC, 1125 Trenton-Harbourton Rd., Titusville, NJ
08560.
Janssen Pharmaceuticals, Inc.
NDA 018029 ..........
NDA 018082 ..........
jbell on DSKJLSW7X2PROD with NOTICES
CMS will collect this information by
electronic means when possible, as well
as by mail, fax, telephone, technical
discussions, and in-person interviews.
CMS may also utilize observational
techniques to collect this information.
Form Number: CMS–10710 (OMB
control number: 0938-New); Frequency:
Occasionally; Affected Public:
Individuals or Households; Private
Sector (business or other for-profits, notfor-profit institutions), State, Local or
Tribal governments; Federal
government; and Universities; Number
of Respondents: 1,001,750; Number of
Responses: Varied, dependent upon the
data collection method used. The
possible response time to complete a
questionnaire or survey may be 3
minutes or up to 2 hours to participate
in an interview.; Total Annual Hours:
51,175. (For questions regarding this
collection contact Aaron Lartey at 410–
786–7866).
NDA 021203 ..........
NDA 021543 ..........
NDA 021604 ..........
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18:29 May 13, 2020
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AbbVie Inc.
Auxilium Pharmaceuticals, Inc., 1400 Atwater Dr., Malvern,
PA 19355.
Moberg Pharma North America LLC, 7 East Frederick
Place, Suite 100, Cedar Knolls, NJ 07927.
E:\FR\FM\14MYN1.SGM
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Agencies
[Federal Register Volume 85, Number 94 (Thursday, May 14, 2020)]
[Notices]
[Pages 28948-28950]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-10282]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifiers CMS-10275, CMS-R-64, and CMS-10710]
Agency Information Collection Activities: Submission for OMB
Review; Comment Request
AGENCY: Centers for Medicare & Medicaid Services, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Centers for Medicare & Medicaid Services (CMS) is
announcing an opportunity for the public to comment on CMS' intention
to collect
[[Page 28949]]
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.
DATES: Comments on the collection(s) of information must be received by
the OMB desk officer by June 15, 2020.
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:
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 30-day Review--Open for
Public Comments'' or by using the search function.
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 website address at https://www.cms.gov/Regulations-and-Guidance/Legislation/PaperworkReductionActof1995/PRA-Listing.html.
1. Email your request, including your address, phone number, OMB
number, and CMS document identifier, to [email protected].
2. 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: Extension without change
of a currently approved collection; Title of Information Collection:
CAHPS Home Health Care Survey; Use: The national implementation of the
Home Health Care CAHPS Survey is designed to collect ongoing data from
samples of home health care patients who receive skilled services from
Medicare-certified home health agencies.
The survey is necessary because it fulfills the goal of
transparency with the public about home health patient experiences. The
survey is used by Medicare-certified home health agencies to improve
their internal quality assurance in the care that they provide in home
health. The HHCAHPS survey is also used in a Medicare payment program.
Medicare-certified home health agencies (HHAs) must contract with CMS-
approved survey vendors that conduct the HHCAHPS on behalf of the HHAs
to meet their requirements in the Home Health Quality Reporting
Program. Form Number: CMS-10257 (OMB control number: 0938-1066);
Frequency: Yearly; Affected Public: Individuals and Households; Number
of Respondents: 1,195,930; Total Annual Responses: 1,294,820; Total
Annual Hours: 453,239. (For policy questions regarding this collection
contact Lori Teichman at 410-786-6684.)
2. Type of Information Collection Request: Extension without change
of a currently approved collection; Title of Information Collection:
Indirect Medical Education and Direct Graduate Medical Education; Use:
Section 1886(d)(5)(B) of the Social Security Act requires additional
payments to be made under the Medicare Prospective Payment System (PPS)
for the indirect medical educational costs a hospital incurs in
connection with interns and residents (IRs) in approved teaching
programs. In addition, Title 42, Part 413, sections 75 through 83
implement section 1886(d) of the Act by establishing the methodology
for Medicare payment for the costs of direct graduate medical
educational activities. These payments, which are adjustments (add-ons)
to other payments made to a hospital under PPS, are largely determined
by the number of full-time equivalent (FTE) IRs that work at a hospital
during its cost reporting period. In Federal fiscal year (FY) 2018, the
estimated Medicare program payments for indirect medical education
(IME) costs was $6.4 billion. Medicare program payment for direct
graduate medical education (GME) is also based upon the number of FTE-
IRs that work at a hospital. In FY 2018, the estimated Medicare program
payments for GME costs was $3.1 billion.
Since it is important to accurately count the number of IRs FTEs
working at each hospital, original approval was obtained from the
Office of Management and Budget (OMB) in 1985 to collect the IR
information required in 42 CFR 412.105(f) and timeframes for filing.
All Medicare health plans are required to use these standardized
notices. Form Number: CMS-R-64 (OMB control number: 0938-0456);
Frequency: Yearly; Affected Public: State, Local, or Tribal
Governments; Number of Respondents: 1,245; Total Annual Responses:
1,245; Total Annual Hours: 2,490. (For policy questions regarding this
collection contact Owen Osaghae at 410-786-7550.)
3. Type of Information Collection Request: New collection (Request
for a new OMB control number) collection; Title of Information
Collection: Generic Clearance for Improving Customer Experience (OMB
Circular A-11, Section 280 Implementation); Use: Whether seeking a
loan, Social Security benefits, veterans benefits, or other services
provided by the Federal Government, individuals and businesses expect
Government customer services to be efficient and intuitive, just like
services from leading private-sector organizations. Yet the 2016
American Consumer Satisfaction Index and the 2017 Forrester Federal
Customer Experience Index show that, on average, Government services
lag nine percentage points behind the private sector.
A modern, streamlined and responsive customer experience means:
Raising government-wide customer experience to the average of the
private sector service industry; developing indicators for high-impact
Federal programs to monitor progress towards excellent customer
experience and mature digital services; and providing
[[Page 28950]]
the structure (including increasing transparency) and resources to
ensure customer experience is a focal point for agency leadership. To
support this, OMB Circular A-11 Section 280 established government-wide
standards for mature customer experience organizations in government
and measurement. To enable Federal programs to deliver the experience
taxpayers deserve, they must undertake three general categories of
activities: Conduct ongoing customer research, gather and share
customer feedback, and test services and digital products.
These data collection efforts may be either qualitative or
quantitative in nature or may consist of mixed methods. Additionally,
data may be collected via a variety of means, including but not limited
to electronic or social media, direct or indirect observation (i.e., in
person, video and audio collections), interviews, questionnaires,
surveys, and focus groups. The Centers for Medicare and Medicaid
Services (CMS) will limit its inquiries to data collections that
solicit strictly voluntary opinions or responses. Steps will be taken
to ensure anonymity of respondents in each activity covered by this
request.
The results of the data collected will be used to improve the
delivery of Federal services and programs. It will include the creation
of personas, customer journey maps, and reports and summaries of
customer feedback data and user insights. It will also provide
government-wide data on customer experience that can be displayed on
performance.gov to help build transparency and accountability of
Federal programs to the customers they serve.
CMS will collect this information by electronic means when
possible, as well as by mail, fax, telephone, technical discussions,
and in-person interviews. CMS may also utilize observational techniques
to collect this information.
Form Number: CMS-10710 (OMB control number: 0938-New); Frequency:
Occasionally; Affected Public: Individuals or Households; Private
Sector (business or other for-profits, not-for-profit institutions),
State, Local or Tribal governments; Federal government; and
Universities; Number of Respondents: 1,001,750; Number of Responses:
Varied, dependent upon the data collection method used. The possible
response time to complete a questionnaire or survey may be 3 minutes or
up to 2 hours to participate in an interview.; Total Annual Hours:
51,175. (For questions regarding this collection contact Aaron Lartey
at 410-786-7866).
Dated: May 8, 2020.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office of Strategic Operations and
Regulatory Affairs.
[FR Doc. 2020-10282 Filed 5-13-20; 8:45 am]
BILLING CODE 4120-01-P