Administration on Intellectual and Developmental Disabilities (AIDD); Notice of Meeting, 6727-6728 [2015-02514]
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Federal Register / Vol. 80, No. 25 / Friday, February 6, 2015 / Notices
asabaliauskas on DSK5VPTVN1PROD with NOTICES
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: Medicaid
Program; Eligibility Changes under the
Affordable Care Act of 2010; Use: The
eligibility systems are essential to the
goal of increasing coverage in insurance
affordability programs while reducing
administrative burden on states and
consumers. The electronic transmission
and automation of data transfers are key
elements in managing the expected
insurance affordability program
caseload that started in 2014.
Accomplishing the same work without
these information collection
requirements would not be feasible.
Form Number: CMS–10410 (OMB
control number 0938–1147); Frequency:
Occasionally; Affected Public:
Individuals or households, and State,
Local, and Tribal Governments; Number
of Respondents: 25,500,096; Total
Annual Responses: 76,500,149; Total
Annual Hours: 21,278,142. (For policy
questions regarding this collection
contact Brenda Sheppard at 410–786–
8534).
2. Type of Information Collection
Request: Extension of a currently
approved collection; Title of
Information Collection: Income and
Eligibility Verification System Reporting
and Supporting Regulations; Use: A
state Medicaid agency that currently
obtains and uses information from
certain sources, or with more frequency
than specified, could continue to do so
to the extent that the verifications are
useful and not redundant. An agency
that has found it effective to verify all
wage or benefit information with
another agency or with the recipient is
encouraged to continue these practices
if it chooses. On the other hand, the
agency may implement an approved
targeting plan under 42 CFR 435.953.
The agency’s experience should guide
its decision whether to exceed these
regulatory requirements on income and
eligibility verification. While states may
target resources when verifying income
of course, agencies are still held
accountable for their accuracy in
eligibility determinations. Form
Number: CMS–R–74 (OMB control
number 0938–0467); Frequency:
Occasionally; Affected Public: State,
Local, or Tribal Governments; Number
of Respondents: 50; Total Annual
Responses: 71; Total Annual Hours:
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18:52 Feb 05, 2015
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134,865. (For policy questions regarding
this collection contact Brenda Sheppard
at 410–786–8534).
3. Type of Information Collection
Request: Revision of a currently
approved collection; Title of
Information Collection: Hospital and
Hospital Health Care Complex Cost
Report; Use: Providers of services
participating in the Medicare program
are required under sections 1815(a) and
1861(v)(1)(A) of the Social Security Act
(42 U.S.C. 1395g) to submit annual
information to achieve settlement of
costs for health care services rendered to
Medicare beneficiaries. In addition,
regulations at 42 CFR 413.20 and 413.24
require adequate cost data and cost
reports from providers on an annual
basis.
We are requesting the Office of
Management and Budget review and
approve this revision to the Form CMS–
2552–10, Hospital and Hospital Health
Care Complex Cost Report. These cost
reports are filed annually by hospitals
participating in the Medicare program to
determine the reasonable costs incurred
to provide medical services to patients.
The revisions made to the hospital cost
report are in accordance with the
statutory requirement for hospice
payment reform in § 3132 of the Patient
Protection and Affordable Care Act
(ACA) (March 23, 2010) and the
statutory requirement establishing a
prospective payment system for
Federally Qualified Health Centers in
§ 10501(i)(3)(A) of the ACA, codified in
section 1834(o) of the Act. Form
Number: CMS–2552–10 (OMB control
number 0938–0050); Frequency: Yearly;
Affected Public: State, Local, or Tribal
Governments, private sector (for-profit
and not-for-profit institutions); Number
of Respondents: 6,157; Total Annual
Responses: 6,157; Total Annual Hours:
4,143,661. (For policy questions
regarding this collection contact Gail
Duncan at 410–786–7278).
4. Type of Information Collection
Request: Revision of a currently
approved collection; Title of
Information Collection: Medicare
Enrollment Application: Reassignment
of Medicare Benefits; Use: The primary
function of the CMS 855R enrollment
application is to allow physicians and
non-physician practitioners to reassign
their Medicare benefits to a group
practice and to gather information from
the individual that tells us who he/she
is, where he or she renders services, and
information necessary to establish
correct claims payment. The goal of
periodically evaluating and revising the
CMS 855R enrollment application is to
simplify and clarify the information
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6727
collection without jeopardizing our
need to collect specific information.
At this time, CMS is making very few
minor revisions to the CMS 855R
(Reassignment of Benefits) Medicare
enrollment application (OMB No. 0938–
1179). Two sections within the form are
being reversed to maintain sync with
online and paper forms. The previously
approved CMS 855R section 2 collected
information regarding the individual
practitioner who is reassigning benefits
and section 3 collected information
regarding the organization/group
receiving the reassigned benefits. These
two sections have been reversed so that
section 2 now collects information on
the regarding the organization/group
receiving the reassigned benefits and
section 3 now collects information on
the individual practitioner who is
reassigning benefits. No information or
data collection within these sections
was revised. The sections were merely
re-sequenced and re-numbered to
maintain sync between online and
paper forms. With the exception of this
section reversal and adding the word
‘‘optional’’ to sections 4 and 5 (primary
practice location and contact person
information), there are no other
revisions. These revisions offer no new
data collection in this revision package.
The addition of the optional choice in
sections 4 and 5 could potentially
reduce the burden to providers who
choose not to complete either or both
optional sections. Form Number: CMS–
855R (OMB control number 0938–1179);
Frequency: Occasionally; Affected
Public: State, Local, or Tribal
Governments, private sector (for-profit
and not-for-profit institutions); Number
of Respondents: 379,619; Total Annual
Responses: 379,619; Total Annual
Hours: 94,905. (For policy questions
regarding this collection contact Kim
McPhillips at 410–786–5374).
Dated: February 3, 2015.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office
of Strategic Operations and Regulatory
Affairs.
[FR Doc. 2015–02414 Filed 2–5–15; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Community Living
Administration on Intellectual and
Developmental Disabilities (AIDD);
Notice of Meeting
President’s Committee for
People with Intellectual Disabilities
(PCPID).
AGENCY:
E:\FR\FM\06FEN1.SGM
06FEN1
6728
ACTION:
Federal Register / Vol. 80, No. 25 / Friday, February 6, 2015 / Notices
Notice of meeting.
Thursday, February 19, 2015
from 9:00 a.m. to 4:30 p.m.; and Friday,
February 20, 2015 from 9:00 a.m. to 2:00
p.m. (EST)
These meetings will be open to the
general public.
ADDRESSES: These meetings will be held
in the U.S. Department of Health and
Human Services/Hubert H. Humphrey
Building located at 200 Independence
Avenue SW., Conference Room 505A,
Washington, DC 20201.
Individuals who would like to
participate via conference call may do
so by dialing toll-free 888–935–0260,
when prompted enter pass code:
3656064. Individuals whose full
participation in the meeting will require
special accommodations (e.g., sign
language interpreting services, assistive
listening devices, materials in
alternative format such as large print or
Braille) should notify Dr. MJ Karimi,
PCPID Team Lead, via email at
MJ.Karimie@acl.hhs.gov, or via
telephone at 202–357–3588, no later
than Friday, February 13, 2015. The
PCPID will attempt to accommodate
requests made after that date, but cannot
guarantee the ability to grant requests
received after this deadline. All meeting
sites are barrier free, consistent with the
Americans with Disabilities Act (ADA)
and the Federal Advisory Committee
Act (FACA).
Agenda: The Committee Members
will discuss preparation of the PCPID
2015 Report to the President, including
its content and format, and related data
collection and analysis required to
complete the writing of the Report. They
will also receive presentations from
selected experts in the field of
Technology for People with Intellectual
and Developmental Disabilities.
Additional Information: For further
information, please contact Dr. MJ
Karimi, Team Lead, President’s
Committee for People with Intellectual
Disabilities, One Massachusetts Avenue
NW., Room 4206, Washington, DC
20201. Telephone: 202–357–3588. Fax:
202–205–8037. Email: MJ.Karimie@
acl.hhs.gov.
SUPPLEMENTARY INFORMATION: The
PCPID acts in an advisory capacity to
the President and the Secretary of
Health and Human Services, through
the Administration on Intellectual and
Developmental Disabilities, on a broad
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DATES:
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range of topics relating to programs,
services and supports for persons with
intellectual disabilities. The PCPID
Executive Order stipulates that the
Committee shall: (1) Provide such
advice concerning intellectual
disabilities as the President or the
Secretary of Health and Human Services
may request; and (2) provide advice to
the President concerning the following
for people with intellectual disabilities:
(A) Expansion of educational
opportunities; (B) promotion of
homeownership; (C) assurance of
workplace integration; (D) improvement
of transportation options; (E) expansion
of full access to community living; and
(F) increasing access to assistive and
universally designed technologies.
Dated: January 28, 2015.
Aaron Bishop,
Commissioner, Administration on Intellectual
and Developmental Disabilities (AIDD).
[FR Doc. 2015–02514 Filed 2–5–15; 8:45 am]
BILLING CODE P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2010–N–0161]
Agency Information Collection
Activities; Submission for Office of
Management and Budget Review;
Comment Request; Export of Food and
Drug Administration Regulated
Products: Export Certificates
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
The Food and Drug
Administration (FDA) is announcing
that a proposed collection of
information has been submitted to the
Office of Management and Budget
(OMB) for review and clearance under
the Paperwork Reduction Act of 1995.
DATES: Fax written comments on the
collection of information by March 9,
2015.
ADDRESSES: To ensure that comments on
the information collection are received,
OMB recommends that written
comments be faxed to the Office of
Information and Regulatory Affairs,
OMB, Attn: FDA Desk Officer, FAX:
202–395–7285, or emailed to oira_
submission@omb.eop.gov. All
SUMMARY:
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comments should be identified with the
OMB control number 0910–0498. Also
include the FDA docket number found
in brackets in the heading of this
document.
FDA
PRA Staff, Office of Operations, Food
and Drug Administration, 8455
Colesville Rd., COLE–14526, Silver
Spring, MD 20993–0002, PRAStaff@
fda.hhs.gov.
FOR FURTHER INFORMATION CONTACT:
In
compliance with 44 U.S.C. 3507, FDA
has submitted the following proposed
collection of information to OMB for
review and clearance.
SUPPLEMENTARY INFORMATION:
Export of Food and Drug
Administration Regulated Products:
Export Certificates—(OMB Control
Number 0910–0498)—Extension
In April 1996, a law entitled ‘‘The
FDA Export Reform and Enhancement
Act of 1996’’ (FDAERA) amended
sections 801(e) and 802 of the FD&C Act
(21 U.S.C. 381(e) and 382). It was
designed to ease restrictions on
exportation of unapproved
pharmaceuticals, biologics, and devices
regulated by FDA. Section 801(e)(4) of
the FDAERA provides that persons
exporting certain FDA regulated
products may request FDA to certify
that the products meet the requirements
of 801(e) and 802 or other requirements
of the FD&C Act. This section of the law
requires FDA to issue certification
within 20 days of receipt of the request
and to charge firms up to $175 for the
certifications.
This section of the FD&C Act
authorizes FDA to issue export
certificates for regulated
pharmaceuticals, biologics, and devices
that are legally marketed in the United
States, as well as for these same
products that are not legally marketed
but are acceptable to the importing
country, as specified in sections 801(e)
and 802 of the FD&C Act. FDA has
developed four types of certificates that
satisfy the requirements of section
801(e)(4)(B) of the FD&C Act: (1)
Certificates to Foreign Governments, (2)
Certificates of Exportability, (3)
Certificates of a Pharmaceutical Product,
and (4) Non-Clinical Research Use Only
Certificates. Table 1 of this document
lists the different certificates and details
their use:
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]]>Agencies
[Federal Register Volume 80, Number 25 (Friday, February 6, 2015)]
[Notices]
[Pages 6727-6728]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2015-02514]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Community Living
Administration on Intellectual and Developmental Disabilities
(AIDD); Notice of Meeting
AGENCY: President's Committee for People with Intellectual Disabilities
(PCPID).
[[Page 6728]]
ACTION: Notice of meeting.
-----------------------------------------------------------------------
DATES: Thursday, February 19, 2015 from 9:00 a.m. to 4:30 p.m.; and
Friday, February 20, 2015 from 9:00 a.m. to 2:00 p.m. (EST)
These meetings will be open to the general public.
ADDRESSES: These meetings will be held in the U.S. Department of Health
and Human Services/Hubert H. Humphrey Building located at 200
Independence Avenue SW., Conference Room 505A, Washington, DC 20201.
Individuals who would like to participate via conference call may
do so by dialing toll-free 888-935-0260, when prompted enter pass code:
3656064. Individuals whose full participation in the meeting will
require special accommodations (e.g., sign language interpreting
services, assistive listening devices, materials in alternative format
such as large print or Braille) should notify Dr. MJ Karimi, PCPID Team
Lead, via email at MJ.Karimie@acl.hhs.gov, or via telephone at 202-357-
3588, no later than Friday, February 13, 2015. The PCPID will attempt
to accommodate requests made after that date, but cannot guarantee the
ability to grant requests received after this deadline. All meeting
sites are barrier free, consistent with the Americans with Disabilities
Act (ADA) and the Federal Advisory Committee Act (FACA).
Agenda: The Committee Members will discuss preparation of the PCPID
2015 Report to the President, including its content and format, and
related data collection and analysis required to complete the writing
of the Report. They will also receive presentations from selected
experts in the field of Technology for People with Intellectual and
Developmental Disabilities.
Additional Information: For further information, please contact Dr.
MJ Karimi, Team Lead, President's Committee for People with
Intellectual Disabilities, One Massachusetts Avenue NW., Room 4206,
Washington, DC 20201. Telephone: 202-357-3588. Fax: 202-205-8037.
Email: MJ.Karimie@acl.hhs.gov.
SUPPLEMENTARY INFORMATION: The PCPID acts in an advisory capacity to
the President and the Secretary of Health and Human Services, through
the Administration on Intellectual and Developmental Disabilities, on a
broad range of topics relating to programs, services and supports for
persons with intellectual disabilities. The PCPID Executive Order
stipulates that the Committee shall: (1) Provide such advice concerning
intellectual disabilities as the President or the Secretary of Health
and Human Services may request; and (2) provide advice to the President
concerning the following for people with intellectual disabilities: (A)
Expansion of educational opportunities; (B) promotion of homeownership;
(C) assurance of workplace integration; (D) improvement of
transportation options; (E) expansion of full access to community
living; and (F) increasing access to assistive and universally designed
technologies.
Dated: January 28, 2015.
Aaron Bishop,
Commissioner, Administration on Intellectual and Developmental
Disabilities (AIDD).
[FR Doc. 2015-02514 Filed 2-5-15; 8:45 am]
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