Agency Information Collection Activities: Submission for OMB Review; Comment Request, 62741-62742 [2016-21873]
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62741
Federal Register / Vol. 81, No. 176 / Monday, September 12, 2016 / Notices
Respondents will include individuals
who call poison centers about exposures
related to the select public health
emergencies. These respondents include
adults, 18 years and older; adolescents,
15 to less than 18 years; and parents or
guardians on behalf of their children
less than 15 years of age.
The total estimate of 300 annual
respondents is based on poison center
experience which assumes two
incidents per year with approximately
150 respondents per event. The average
burden per respondent is approximately
40 minutes for the call-back
questionnaire. We anticipate a total
annualized burden of 200 hours.
There is no cost to the respondents
other than their time.
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Type of respondent
Form name
Adult Poison Center Callers ...........................
Adolescent Poison Center Callers ..................
Parent or Guardian Poison Center Callers .....
Sample Questionnaire—Adults ......................
Sample Questionnaire—Adolescent ..............
Sample Questionnaire—Parent or Guardian
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. 2016–21885 Filed 9–9–16; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifiers: CMS–588, CMS–
10146, CMS–10185, CMS–10261, and CMS–
10631]
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 any of the
following subjects: 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
sradovich on DSK3GMQ082PROD with NOTICES
SUMMARY:
VerDate Sep<11>2014
18:40 Sep 09, 2016
Jkt 238001
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 October 12, 2016.
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.
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
https://www.cms.hhs.gov/
PaperworkReductionActof1995.
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:
Reports Clearance Office at (410) 786–
1326.
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
PO 00000
Frm 00041
Fmt 4703
Sfmt 4703
210
30
60
Number of
responses per
respondent
1
1
1
Average
burden per
response
(in hours)
40/60
40/60
40/60
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: Electronic
Funds Transfer Authorization
Agreement; Use: The information is
needed to allow providers to receive
funds electronically in their bank
accounts. Form Number: CMS–588
(OMB control number: 0938–0626);
Frequency: On occasion; Affected
Public: Business or other for-profit, Notfor-profit institutions; Number of
Respondents: 45,807; Total Annual
Responses: 45,807; Total Annual Hours:
22,906. (For policy questions regarding
this collection contact Kimberly
McPhillips at 410–786–4645.)
2. Type of Information Collection
Request: Revision of a currently
approved collection; Title of
Information Collection: Medicare Part D
Reporting Requirements and Supporting
Regulations; Use: Data collected via
Medicare Part D Reporting
Requirements will be an integral
resource for oversight, monitoring,
compliance and auditing activities
necessary to ensure quality provision of
the Medicare Prescription Drug Benefit
to beneficiaries. For all reporting
sections, data are reported electronically
to CMS. Each reporting section is
reported at one of the following levels:
Contract (data should be entered at the
H#, S#, R#, or E# level) or Plan (data
E:\FR\FM\12SEN1.SGM
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sradovich on DSK3GMQ082PROD with NOTICES
62742
Federal Register / Vol. 81, No. 176 / Monday, September 12, 2016 / Notices
should be entered at the Plan Benefit
Package (PBP level, e.g. Plan 001 for
contract H#, R#, S#, or E). Sponsors
should retain documentation and data
records related to their data
submissions. Data will be validated,
analyzed, and utilized for trend
reporting by the Division of Clinical and
Operational Performance (DCOP) within
the Medicare Drug Benefit and C&D
Data Group. If outliers or other data
anomalies are detected, DCOP will work
in collaboration with other Divisions
within CMS for follow-up and
resolution. For CY2017 Reporting
Requirements, the following 7 reporting
sections will be reported and collected
at the Contract-level or Plan-level:
Enrollment and Disenrollment, Retail,
Home Infusion, and Long-Term Care
Pharmacy Access, Medication Therapy
Management (MTM) Programs,
Grievances, Improving Drug Utilization
Review Controls, Coverage
Determinations and Redeterminations,
and Employer/Union Sponsored
Sponsors. Form Number: CMS–10185
(OMB control number: 0938–0992);
Frequency: Annually and semiannually; Affected Public: Private sector
(Business or other for-profits); Number
of Respondents: 561; Total Annual
Responses: 11,438; Total Annual Hours:
14,750. (For policy questions regarding
this collection contact Chanelle Jones at
410–786–8008.)
3. Type of Information Collection
Request: Revision of a currently
approved collection; Title of
Information Collection: Part C Medicare
Advantage Reporting Requirements and
Supporting Regulations in 42 CFR
422.516(a); Use: Medicare Advantage
Organizations (MAOs) must have an
effective procedure to develop, compile,
evaluate, and report to CMS, to its
enrollees, and to the general public, at
the times and in the manner that CMS
requires, and while safeguarding the
confidentiality of the doctor-patient
relationship, statistics and other
information with respect to: The cost of
its operations; the patterns of service
utilization; the availability,
accessibility, and acceptability of its
services; to the extent practical,
developments in the health status of its
enrollees; information demonstrating
that the MAO has a fiscally sound
operation; and other matters that CMS
may require. CMS also has oversight
authority over cost plans which
includes establishment of reporting
requirements. This revision would add
five new data elements to the reporting
section: Organization Determinations
and Reconsiderations. These new data
elements are needed to obtain more
VerDate Sep<11>2014
18:40 Sep 09, 2016
Jkt 238001
information about case reopenings. The
revision would also suspend the
Sponsor Oversight of Agents reporting
section beginning 2017 so that the
reporting section can be reassessed
based on burden and usage. Form
Number: CMS–10261 (OMB control
number: 0938–1054); Frequency: Yearly
and Semi-annually; Affected Public:
Private sector (Business or other Forprofits); Number of Respondents: 544;
Total Annual Responses: 3,508; Total
Annual Hours: 160,215. (For policy
questions regarding this collection
contact Terry Lied at 410–786–8973.)
4. Type of Information Collection
Request: Revision of a currently
approved collection; Title of
Information Collection: Notice of Denial
of Medicare Prescription Drug Coverage;
Use: The notice provides information to
enrollees when prescription drug
coverage has been denied, in whole or
in part, by their Part D plans. The notice
must be readable, understandable, and
state the specific reasons for the denial.
The notice must also remind enrollees
about their rights and protections
related to requests for prescription drug
coverage and include an explanation of
both the standard and expedited
redetermination processes and the rest
of the appeal process. Form Number:
CMS–10146 (OMB control number:
0938–0976); Frequency: Occasionally;
Affected Public: Private sector (Business
or other for-profits); Number of
Respondents: 580; Total Annual
Responses: 1,902,055; Total Annual
Hours: 475,514. (For policy questions
regarding this collection contact Amber
Casserly at 410–786–0976.)
5. Type of Information Collection
Request: New collection (request for a
new OMB control number); Title of
Information Collection: The PACE
Organization Application Process in 42
CFR part 460; Use: In general, Programs
of All-Inclusive Care for the Elderly
(PACE) services are provided through a
PACE Organization (PO). An entity
wishing to become a PO must submit an
application to CMS that describes how
the entity meets all the requirements in
the PACE program. An entity’s
application must be accompanied by an
assurance from the State Administering
Agency (SAA) of the State in which the
PO is going to be located.
Initial application requirements for
the PACE program are currently set
forth in 42 CFR 460.12 and in the PACE
Manual, Ch. 17. Until recently, the
submission of initial and service area
expansion (SAE) PACE applications and
supporting information was in paper
format. These applications are often
hundreds of pages long, expensive to
reproduce and transmit, and
PO 00000
Frm 00042
Fmt 4703
Sfmt 9990
administratively inefficient, as staff
reviewing different parts of the
application are located in different
physical locations and must receive
hard copies of the material. However,
beginning in 2016, initial PACE
applications are being submitted via a
new automated, electronic submission
process. As with initial applications, an
application also must be submitted for
a PO that seeks to expand its service
area and/or add a new service site, and
with OMB approval, an automated
application process will now also be
required of PACE organizations
submitting service area expansion
applications.
While this collection is being
submitted to OMB as a ‘‘New’’ package,
the collection is not new. The collection
is currently approved by OMB under
control number 0938–0790 (CMS–R–
244). Based on internal review we
intend to remove the application from
that package but, before doing so, we
need approval of the application under
a new OMB control number. This will
avoid lapses in OMB’s approval along
with any violations of the PRA.
As is, the currently approved CMS–R–
244 package is lengthy and somewhat
time consuming to review. We believe
the change will help streamline the
public and OMB’s review of the
application as well as the remaining
requirements and burden under CMS–
R–244. The 60-day notice published in
the Federal Register on December 8,
2015 (80 FR 76193). The 30-day notice
published on May 2, 2016 (81 FR
26234). Both published under CMS–R–
244. We are republishing the 30-day
notice under the new CMS ID number
(CMS–10631) and the tentative OMB
control number (0938–New). Otherwise,
all changes are nonsubstantive.
Form Number: CMS–10631 (OMB
control number: 0938–New); Frequency:
Once and occasionally; Affected Public:
Private sector (Business or other forprofits and Not-for-profit institutions)
and State, Local, or Tribal Governments;
Number of Respondents: 730; Total
Annual Responses: 84; Total Annual
Hours: 4,576. (For policy questions
regarding this collection contact Debbie
Vanhoven at 410–786–6625.)
Dated: September 7, 2016.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office
of Strategic Operations and Regulatory
Affairs.
[FR Doc. 2016–21873 Filed 9–9–16; 8:45 am]
BILLING CODE 4120–01–P
E:\FR\FM\12SEN1.SGM
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Agencies
[Federal Register Volume 81, Number 176 (Monday, September 12, 2016)]
[Notices]
[Pages 62741-62742]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-21873]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifiers: CMS-588, CMS-10146, CMS-10185, CMS-10261, and
CMS-10631]
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 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 any of the following subjects: 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 October 12, 2016.
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.
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 https://www.cms.hhs.gov/PaperworkReductionActof1995.
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: Reports Clearance Office at (410) 786-
1326.
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: Electronic Funds
Transfer Authorization Agreement; Use: The information is needed to
allow providers to receive funds electronically in their bank accounts.
Form Number: CMS-588 (OMB control number: 0938-0626); Frequency: On
occasion; Affected Public: Business or other for-profit, Not-for-profit
institutions; Number of Respondents: 45,807; Total Annual Responses:
45,807; Total Annual Hours: 22,906. (For policy questions regarding
this collection contact Kimberly McPhillips at 410-786-4645.)
2. Type of Information Collection Request: Revision of a currently
approved collection; Title of Information Collection: Medicare Part D
Reporting Requirements and Supporting Regulations; Use: Data collected
via Medicare Part D Reporting Requirements will be an integral resource
for oversight, monitoring, compliance and auditing activities necessary
to ensure quality provision of the Medicare Prescription Drug Benefit
to beneficiaries. For all reporting sections, data are reported
electronically to CMS. Each reporting section is reported at one of the
following levels: Contract (data should be entered at the H#, S#, R#,
or E# level) or Plan (data
[[Page 62742]]
should be entered at the Plan Benefit Package (PBP level, e.g. Plan 001
for contract H#, R#, S#, or E). Sponsors should retain documentation
and data records related to their data submissions. Data will be
validated, analyzed, and utilized for trend reporting by the Division
of Clinical and Operational Performance (DCOP) within the Medicare Drug
Benefit and C&D Data Group. If outliers or other data anomalies are
detected, DCOP will work in collaboration with other Divisions within
CMS for follow-up and resolution. For CY2017 Reporting Requirements,
the following 7 reporting sections will be reported and collected at
the Contract-level or Plan-level: Enrollment and Disenrollment, Retail,
Home Infusion, and Long-Term Care Pharmacy Access, Medication Therapy
Management (MTM) Programs, Grievances, Improving Drug Utilization
Review Controls, Coverage Determinations and Redeterminations, and
Employer/Union Sponsored Sponsors. Form Number: CMS-10185 (OMB control
number: 0938-0992); Frequency: Annually and semi-annually; Affected
Public: Private sector (Business or other for-profits); Number of
Respondents: 561; Total Annual Responses: 11,438; Total Annual Hours:
14,750. (For policy questions regarding this collection contact
Chanelle Jones at 410-786-8008.)
3. Type of Information Collection Request: Revision of a currently
approved collection; Title of Information Collection: Part C Medicare
Advantage Reporting Requirements and Supporting Regulations in 42 CFR
422.516(a); Use: Medicare Advantage Organizations (MAOs) must have an
effective procedure to develop, compile, evaluate, and report to CMS,
to its enrollees, and to the general public, at the times and in the
manner that CMS requires, and while safeguarding the confidentiality of
the doctor-patient relationship, statistics and other information with
respect to: The cost of its operations; the patterns of service
utilization; the availability, accessibility, and acceptability of its
services; to the extent practical, developments in the health status of
its enrollees; information demonstrating that the MAO has a fiscally
sound operation; and other matters that CMS may require. CMS also has
oversight authority over cost plans which includes establishment of
reporting requirements. This revision would add five new data elements
to the reporting section: Organization Determinations and
Reconsiderations. These new data elements are needed to obtain more
information about case reopenings. The revision would also suspend the
Sponsor Oversight of Agents reporting section beginning 2017 so that
the reporting section can be reassessed based on burden and usage. Form
Number: CMS-10261 (OMB control number: 0938-1054); Frequency: Yearly
and Semi-annually; Affected Public: Private sector (Business or other
For-profits); Number of Respondents: 544; Total Annual Responses:
3,508; Total Annual Hours: 160,215. (For policy questions regarding
this collection contact Terry Lied at 410-786-8973.)
4. Type of Information Collection Request: Revision of a currently
approved collection; Title of Information Collection: Notice of Denial
of Medicare Prescription Drug Coverage; Use: The notice provides
information to enrollees when prescription drug coverage has been
denied, in whole or in part, by their Part D plans. The notice must be
readable, understandable, and state the specific reasons for the
denial. The notice must also remind enrollees about their rights and
protections related to requests for prescription drug coverage and
include an explanation of both the standard and expedited
redetermination processes and the rest of the appeal process. Form
Number: CMS-10146 (OMB control number: 0938-0976); Frequency:
Occasionally; Affected Public: Private sector (Business or other for-
profits); Number of Respondents: 580; Total Annual Responses:
1,902,055; Total Annual Hours: 475,514. (For policy questions regarding
this collection contact Amber Casserly at 410-786-0976.)
5. Type of Information Collection Request: New collection (request
for a new OMB control number); Title of Information Collection: The
PACE Organization Application Process in 42 CFR part 460; Use: In
general, Programs of All-Inclusive Care for the Elderly (PACE) services
are provided through a PACE Organization (PO). An entity wishing to
become a PO must submit an application to CMS that describes how the
entity meets all the requirements in the PACE program. An entity's
application must be accompanied by an assurance from the State
Administering Agency (SAA) of the State in which the PO is going to be
located.
Initial application requirements for the PACE program are currently
set forth in 42 CFR 460.12 and in the PACE Manual, Ch. 17. Until
recently, the submission of initial and service area expansion (SAE)
PACE applications and supporting information was in paper format. These
applications are often hundreds of pages long, expensive to reproduce
and transmit, and administratively inefficient, as staff reviewing
different parts of the application are located in different physical
locations and must receive hard copies of the material. However,
beginning in 2016, initial PACE applications are being submitted via a
new automated, electronic submission process. As with initial
applications, an application also must be submitted for a PO that seeks
to expand its service area and/or add a new service site, and with OMB
approval, an automated application process will now also be required of
PACE organizations submitting service area expansion applications.
While this collection is being submitted to OMB as a ``New''
package, the collection is not new. The collection is currently
approved by OMB under control number 0938-0790 (CMS-R-244). Based on
internal review we intend to remove the application from that package
but, before doing so, we need approval of the application under a new
OMB control number. This will avoid lapses in OMB's approval along with
any violations of the PRA.
As is, the currently approved CMS-R-244 package is lengthy and
somewhat time consuming to review. We believe the change will help
streamline the public and OMB's review of the application as well as
the remaining requirements and burden under CMS-R-244. The 60-day
notice published in the Federal Register on December 8, 2015 (80 FR
76193). The 30-day notice published on May 2, 2016 (81 FR 26234). Both
published under CMS-R-244. We are republishing the 30-day notice under
the new CMS ID number (CMS-10631) and the tentative OMB control number
(0938-New). Otherwise, all changes are nonsubstantive.
Form Number: CMS-10631 (OMB control number: 0938-New); Frequency:
Once and occasionally; Affected Public: Private sector (Business or
other for-profits and Not-for-profit institutions) and State, Local, or
Tribal Governments; Number of Respondents: 730; Total Annual Responses:
84; Total Annual Hours: 4,576. (For policy questions regarding this
collection contact Debbie Vanhoven at 410-786-6625.)
Dated: September 7, 2016.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office of Strategic Operations and
Regulatory Affairs.
[FR Doc. 2016-21873 Filed 9-9-16; 8:45 am]
BILLING CODE 4120-01-P