Agency Information Collection Activities: Proposed Collection; Comment Request, 65400-65401 [2014-26041]
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65400
Federal Register / Vol. 79, No. 213 / Tuesday, November 4, 2014 / Notices
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. 2014–26132 Filed 11–3–14; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
Advisory Committee on Breast Cancer
in Young Women (ACBCYW)
rmajette on DSK3VPTVN1PROD with NOTICES
In accordance with section 10(a)(2) of
the Federal Advisory Committee Act
(Pub. L. 92–463), the Centers for Disease
Control and Prevention (CDC),
announces the following meeting of the
aforementioned committee:
Times and Dates: 9:00 a.m.–5:30 p.m. EST,
December 4, 2014; 8:00 a.m.–12:00 p.m. EST,
December 5, 2014.
Place: CDC, 4770 Buford Highway,
Chamblee Building 107 1B/1C, Atlanta,
Georgia 30341.
This meeting is also accessible by
teleconference and web access.
Teleconference and web access login
information is as follows:
Toll-Free Telephone: 1–800–621–3587,
Participant passcode: 9679129. There is also
a toll number for anyone outside of the USA:
TOLL NUMBER: 1–517–308–9263,
Participant passcode: 96791NET
CONFERENCE AND WEB URL: For
December 4, 2014: https://
www.mymeetings.com/nc/join/ Conference
number: PW9240020, Audience passcode:
9679129.
For December 5, 2014: https://
www.mymeetings.com/nc/join/ Conference
number: PW9240028, Audience passcode:
9679129.
Participants can join the event directly at:
https://www.mymeetings.com/nc/
join.php?i=PW9240020&p=9679129&t=c.
Status: Open to the public, limited only by
the space and phone lines available.
Purpose: The committee provides advice
and guidance to the Secretary, HHS; the
Assistant Secretary for Health; and the
Director, CDC, regarding the formative
research, development, implementation and
evaluation of evidence-based activities
designed to prevent breast cancer
(particularly among those at heightened risk)
and promote the early detection and support
of young women who develop the disease.
The advice provided by the Committee will
assist in ensuring scientific quality,
timeliness, utility, and dissemination of
credible appropriate messages and resource
materials.
Matters for Discussion: The agenda will
include discussions on the current and
emerging topics related to breast cancer in
young women. These may include public
health communication, breast cancer in
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young women digital and social media
campaigns, and CDC updates. Topics will
address efforts increase awareness around
breast cancer risk, breast health, symptoms,
diagnosis, and treatment of breast cancer in
young women.
Agenda items are subject to change as
priorities dictate.
Online Registration Required: In order to
expedite the security clearance process
required for entry into a Federal building, all
ACBCYW attendees must register for the
meeting online at least 7 days in advance at
https://www.cdc.gov/cancer/breast/what_cdc_
is_doing/meetings.htm. Please complete all
the required fields before submitting your
registration and submit no later than
November 28, 2014. Each meeting day,
attendees must provide CDC staff and
security with driver’s license/state issued ID,
or passport.
Contact Person for More Information:
Temeika L. Fairley, Ph.D., Designated Federal
Officer, National Center for Chronic Disease
Prevention and Health Promotion, CDC, 5770
Buford Hwy. NE., Mailstop K52, Atlanta,
Georgia 30341, Telephone (770) 488–4518,
Fax (770) 488–4760. Email: acbcyw@cdc.gov.
The Director, Management Analysis and
Services Office, has been delegated the
authority to sign Federal Register notices
pertaining to announcements of meetings and
other committee management activities, for
both the Centers for Disease Control and
Prevention, and Agency for Toxic Substances
and Disease Registry.
Hepatitis, STD, and TB Prevention, CDC, in
the following areas: strategies, goals, and
priorities for programs; research within the
national centers; and overall strategic
direction and focus of OID and the national
centers.
Matters for Discussion: Discussions will
focus on current responses and national
center priorities.
Agenda items are subject to change as
priorities dictate.
Contact Person for More Information:
Robin Moseley, M.A.T., Designated Federal
Officer, OID, CDC, 1600 Clifton Road NE.,
Mailstop D10, Atlanta, Georgia 30333,
Telephone: (404) 639–4461.
The Director, Management Analysis and
Services Office has been delegated the
authority to sign Federal Register notices
pertaining to announcements of meetings and
other committee management activities, for
both the Centers for Disease Control and
Prevention and the Agency for Toxic
Substances and Disease Registry.
Claudette Grant,
Acting Director, Management Analysis and
Services Office, Centers for Disease Control
and Prevention.
Centers for Medicare & Medicaid
Services
[FR Doc. 2014–26082 Filed 11–3–14; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
Board of Scientific Counselors, Office
of Infectious Diseases (BSC, OID);
Notice of Meeting
In accordance with section 10(a)(2) of
the Federal Advisory Committee Act
(Pub. L. 92–463), the Centers for Disease
Control and Prevention (CDC),
announces the following meeting of the
aforementioned committee:
Time and Date: 10:00–11:00 a.m. EST,
November 20, 2014.
Place: Teleconference.
Status: The meeting is open to the public;
the toll free dial in number is 1–877–951–
7311 with a pass code of 1588067.
Purpose: The BSC, OID, provides advice
and guidance to the Secretary, Department of
Health and Human Services; the Director,
CDC; the Director, OID; and the Directors of
the National Center for Immunization and
Respiratory Diseases, the National Center for
Emerging and Zoonotic Infectious Diseases,
and the National Center for HIV/AIDS, Viral
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Claudette Grant,
Acting Director, Management Analysis and
Services Office, Centers for Disease Control
and Prevention.
[FR Doc. 2014–26083 Filed 11–3–14; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
[Document Identifier: CMS–10527]
Agency Information Collection
Activities: Proposed Collection;
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 (the
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
60 days for public comment on the
proposed action. Interested persons are
invited to send comments regarding our
burden estimates or any other aspect of
this collection of information, including
any of the following subjects: (1) The
necessity and utility of the proposed
information collection for the proper
performance of the agency’s functions;
(2) the accuracy of the estimated
burden; (3) ways to enhance the quality,
utility, and clarity of the information to
SUMMARY:
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Federal Register / Vol. 79, No. 213 / Tuesday, November 4, 2014 / Notices
be collected; and (4) the use of
automated collection techniques or
other forms of information technology to
minimize the information collection
burden.
DATES: Comments must be received by
January 5, 2015.
ADDRESSES: When commenting, please
reference the document identifier or
OMB control number (OCN). To be
assured consideration, comments and
recommendations must be submitted in
any one of the following ways:
1. Electronically. You may send your
comments electronically to https://
www.regulations.gov. Follow the
instructions for ‘‘Comment or
Submission’’ or ‘‘More Search Options’’
to find the information collection
document(s) that are accepting
comments.
2. By regular mail. You may mail
written comments to the following
address: CMS, Office of Strategic
Operations and Regulatory Affairs,
Division of Regulations Development,
Attention: Document Identifier/OMB
Control Number llll, Room C4–26–
05, 7500 Security Boulevard, Baltimore,
Maryland 21244–1850.
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:
rmajette on DSK3VPTVN1PROD with NOTICES
Contents
This notice sets out a summary of the
use and burden associated with the
following information collections. More
detailed information can be found in
each collection’s supporting statement
and associated materials (see
ADDRESSES).
CMS–10527 Annual Eligibility
Redetermination, Product
Discontinuation and Renewal Notices
Under the 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
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15:39 Nov 03, 2014
Jkt 235001
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
requires federal agencies to publish a
60-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.
Information Collection
1. Type of Information Collection
Request: Extension of a currently
approved collection; Title of
Information Collection: Annual
Eligibility Redetermination, Product
Discontinuation and Renewal Notices;
Use: Section 1411(f)(1)(B) of the
Affordable Care Act directs the
Secretary of Health and Human Services
(the Secretary) to establish procedures
to redetermine the eligibility of
individuals on a periodic basis in
appropriate circumstances. Section
1321(a) of the Affordable Care Act
provides authority for the Secretary to
establish standards and regulations to
implement the statutory requirements
related to Exchanges, QHPs and other
components of title I of the Affordable
Care Act. Under section 2703 of the PHS
Act, as added by the Affordable Care
Act, and sections 2712 and 2741 of the
PHS Act, enacted by the Health
Insurance Portability and
Accountability Act of 1996, health
insurance issuers in the group and
individual markets must guarantee the
renewability of coverage unless an
exception applies.
The final rule ‘‘Patient Protection and
Affordable Care Act; Annual Eligibility
Redeterminations for Exchange
Participation and Insurance
Affordability Programs; Health
Insurance Issuer Standards Under the
Affordable Care Act, Including
Standards Related to Exchanges’’ (79 FR
52994), provides that an Exchange may
choose to conduct the annual
redetermination process for a plan year
(1) in accordance with the existing
procedures described in 45 CFR
155.335; (2) in accordance with
procedures described in guidance
issued by the Secretary for the coverage
year; or (3) using an alternative
proposed by the Exchange and approved
by the Secretary. The guidance
document ‘‘Guidance on Annual
Redeterminations for Coverage for
2015’’ contains the procedures that the
Secretary is specifying for the 2015
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65401
coverage year, as noted in (2) above.
These procedures will be adopted by the
Federally-facilitated Exchange. Under
this option, the Exchange will provide
three notices. These notices may be
combined.
The final rule also amends the
requirements for product renewal and
re-enrollment (or non-renewal) notices
to be sent by Qualified Health Plan
(QHP) issuers in the Exchanges and
specifies content for these notices. The
accompanying guidance document
‘‘Form and Manner of Notices When
Discontinuing or Renewing a Product in
the Group or Individual Market’’
provides standard notices for product
discontinuation and renewal to be sent
by issuers of individual market QHPs
and issuers in the individual market.
Issuers in the small group market may
use the draft Federal standard small
group notices released in the June 26,
2014 bulletin ‘‘Draft Standard Notices
When Discontinuing or Renewing a
Product in the Small Group or
Individual Market,’’ or any forms of the
notice otherwise permitted by
applicable laws and regulations. States
that are enforcing the Affordable Care
Act may develop their own standard
notices, for product discontinuances,
renewals, or both, provided the Statedeveloped notices are at least as
protective as the Federal standard
notices. Form Number: CMS–10527;
Frequency: Annual; Affected Public:
Private Sector, State Governments;
Number of Respondents: 2,945; Number
of Responses: 12,224; Total Annual
Hours: 149,186. (For policy questions
regarding this collection, contact Usree
Bandyopadhyay at 410–786–6650.)
Dated: October 29, 2014.
Martique Jones,
Director, Regulations Development Group,
Office of Strategic Operations and Regulatory
Affairs.
[FR Doc. 2014–26041 Filed 11–3–14; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifiers: CMS–10522]
Agency Information Collection
Activities: Submission for OMB
Review; Comment Request
ACTION:
Notice.
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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Agencies
[Federal Register Volume 79, Number 213 (Tuesday, November 4, 2014)]
[Notices]
[Pages 65400-65401]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2014-26041]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifier: CMS-10527]
Agency Information Collection Activities: Proposed Collection;
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 (the 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 60 days for public
comment on the proposed action. Interested persons are invited to send
comments regarding our burden estimates or any other aspect of this
collection of information, including any of the following subjects: (1)
The necessity and utility of the proposed information collection for
the proper performance of the agency's functions; (2) the accuracy of
the estimated burden; (3) ways to enhance the quality, utility, and
clarity of the information to
[[Page 65401]]
be collected; and (4) the use of automated collection techniques or
other forms of information technology to minimize the information
collection burden.
DATES: Comments must be received by January 5, 2015.
ADDRESSES: When commenting, please reference the document identifier or
OMB control number (OCN). To be assured consideration, comments and
recommendations must be submitted in any one of the following ways:
1. Electronically. You may send your comments electronically to
https://www.regulations.gov. Follow the instructions for ``Comment or
Submission'' or ``More Search Options'' to find the information
collection document(s) that are accepting comments.
2. By regular mail. You may mail written comments to the following
address: CMS, Office of Strategic Operations and Regulatory Affairs,
Division of Regulations Development, Attention: Document Identifier/OMB
Control Number ___--, Room C4-26-05, 7500 Security Boulevard,
Baltimore, Maryland 21244-1850.
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:
Contents
This notice sets out a summary of the use and burden associated
with the following information collections. More detailed information
can be found in each collection's supporting statement and associated
materials (see ADDRESSES).
CMS-10527 Annual Eligibility Redetermination, Product Discontinuation
and Renewal Notices
Under the 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 requires federal agencies
to publish a 60-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.
Information Collection
1. Type of Information Collection Request: Extension of a currently
approved collection; Title of Information Collection: Annual
Eligibility Redetermination, Product Discontinuation and Renewal
Notices; Use: Section 1411(f)(1)(B) of the Affordable Care Act directs
the Secretary of Health and Human Services (the Secretary) to establish
procedures to redetermine the eligibility of individuals on a periodic
basis in appropriate circumstances. Section 1321(a) of the Affordable
Care Act provides authority for the Secretary to establish standards
and regulations to implement the statutory requirements related to
Exchanges, QHPs and other components of title I of the Affordable Care
Act. Under section 2703 of the PHS Act, as added by the Affordable Care
Act, and sections 2712 and 2741 of the PHS Act, enacted by the Health
Insurance Portability and Accountability Act of 1996, health insurance
issuers in the group and individual markets must guarantee the
renewability of coverage unless an exception applies.
The final rule ``Patient Protection and Affordable Care Act; Annual
Eligibility Redeterminations for Exchange Participation and Insurance
Affordability Programs; Health Insurance Issuer Standards Under the
Affordable Care Act, Including Standards Related to Exchanges'' (79 FR
52994), provides that an Exchange may choose to conduct the annual
redetermination process for a plan year (1) in accordance with the
existing procedures described in 45 CFR 155.335; (2) in accordance with
procedures described in guidance issued by the Secretary for the
coverage year; or (3) using an alternative proposed by the Exchange and
approved by the Secretary. The guidance document ``Guidance on Annual
Redeterminations for Coverage for 2015'' contains the procedures that
the Secretary is specifying for the 2015 coverage year, as noted in (2)
above. These procedures will be adopted by the Federally-facilitated
Exchange. Under this option, the Exchange will provide three notices.
These notices may be combined.
The final rule also amends the requirements for product renewal and
re-enrollment (or non-renewal) notices to be sent by Qualified Health
Plan (QHP) issuers in the Exchanges and specifies content for these
notices. The accompanying guidance document ``Form and Manner of
Notices When Discontinuing or Renewing a Product in the Group or
Individual Market'' provides standard notices for product
discontinuation and renewal to be sent by issuers of individual market
QHPs and issuers in the individual market. Issuers in the small group
market may use the draft Federal standard small group notices released
in the June 26, 2014 bulletin ``Draft Standard Notices When
Discontinuing or Renewing a Product in the Small Group or Individual
Market,'' or any forms of the notice otherwise permitted by applicable
laws and regulations. States that are enforcing the Affordable Care Act
may develop their own standard notices, for product discontinuances,
renewals, or both, provided the State-developed notices are at least as
protective as the Federal standard notices. Form Number: CMS-10527;
Frequency: Annual; Affected Public: Private Sector, State Governments;
Number of Respondents: 2,945; Number of Responses: 12,224; Total Annual
Hours: 149,186. (For policy questions regarding this collection,
contact Usree Bandyopadhyay at 410-786-6650.)
Dated: October 29, 2014.
Martique Jones,
Director, Regulations Development Group, Office of Strategic Operations
and Regulatory Affairs.
[FR Doc. 2014-26041 Filed 11-3-14; 8:45 am]
BILLING CODE 4120-01-P