Proposed Collection; Comment Request, 2155-2156 [2014-00296]
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Federal Register / Vol. 79, No. 8 / Monday, January 13, 2014 / Notices
7700 Arlington Boulevard, Suite 5101,
Falls Church, VA 22042–5101, or call
703–681–0039.
SUPPLEMENTARY INFORMATION:
Title; Associated Form; and OMB
Number: Women, Infants and Children
Overseas Participant Satisfaction
Survey; OMB Control Number 0720–
0046.
Needs and Uses: The information
collection requirement is necessary to
obtain the participant’s satisfaction
levels with the services provided by the
WIC overseas staff and the overall
program. The findings from the surveys
will be used to determine the success of
the WIC overseas program and if
improvements are necessary.
Affected Public: Individual or
Households
Annual Burden Hours: 37.5
Number of Respondents: 150
Responses per Respondent: 1
Average Burden per Response: 15
minutes
Frequency: On occasion
Respondents are individuals who are
currently receiving WIC overseas
services. The purpose of the WIC
overseas survey is to assess the
participant’s satisfaction level with the
services provided by the WIC overseas
staff and the overall program. The
survey includes questions regarding site
access, customer service, quality of
health information and overall program
satisfaction. The findings of these
surveys will be used to determine the
success of the WIC overseas program
and if improvements are necessary. The
WIC overseas program is a legislatively
mandated program and it is anticipated
that the program will continue
indefinitely. As such, DoD is publishing
this formal notice.
Dated: January 8, 2014.
Aaron Siegel,
Alternate OSD Federal Register Liaison
Officer, Department of Defense.
[FR Doc. 2014–00361 Filed 1–10–14; 8:45 am]
BILLING CODE 5001–06–P
DEPARTMENT OF DEFENSE
Office of the Secretary
[Docket ID DoD–2014–HA–0004]
tkelley on DSK3SPTVN1PROD with NOTICES
Proposed Collection; Comment
Request
Office of the Assistant
Secretary of Defense for Health Affairs,
DoD.
ACTION: Notice.
AGENCY:
In compliance with Section
3506(c)(2)(A) of the Paperwork
SUMMARY:
VerDate Mar<15>2010
16:40 Jan 10, 2014
Jkt 232001
Reduction Act of 1995, the Office of the
Assistant Secretary of Defense for
Health Affairs announces a proposed
public information collection and seeks
public comment on the provisions
thereof. Comments are invited on: (a)
Whether the proposed collection of
information is necessary for the proper
performance of the functions of the
agency, including whether the
information shall have practical utility;
(b) the accuracy of the agency’s estimate
of the burden of the proposed
information collection; (c) ways to
enhance the quality, utility, and clarity
of the information to be collected; and
(d) ways to minimize the burden of the
information collection on respondents,
including through the use of automated
collection techniques or other forms of
information technology.
DATES: Consideration will be given to all
comments received by March 14, 2014.
ADDRESSES: You may submit comments,
identified by docket number and title,
by any of the following methods:
• Federal eRulemaking Portal: https://
www.regulations.gov. Follow the
instructions for submitting comments.
• Mail: Federal Docket Management
System Office, 4800 Mark Center Drive,
East Tower, Suite 02G09, Alexandria,
VA 22350–3100.
Instructions: All submissions received
must include the agency name, docket
number and title for this Federal
Register document. The general policy
for comments and other submissions
from members of the public is to make
these submissions available for public
viewing on the Internet at https://
www.regulations.gov as they are
received without change, including any
personal identifiers or contact
information.
Any associated form(s) for this
collection may be located within this
same electronic docket and downloaded
for review/testing. Follow the
instructions at https://
www.regulations.gov for submitting
comments. Please submit comments on
any given form identified by docket
number, form number, and title.
FOR FURTHER INFORMATION CONTACT: To
request more information on this
proposed information collection or to
obtain a copy of the proposal and
associated collection instruments,
please write to the Defense Health
Agency, Medical Benefits and
Reimbursement Systems, 16401 East
Centretech Parkway, ATTN: Elan Green,
Aurora, CO 80011–9043, or call Defense
Health Agency, Medical Benefits and
Reimbursement Office, at (303) 676–
3907.
SUPPLEMENTARY INFORMATION:
PO 00000
Frm 00009
Fmt 4703
Sfmt 4703
2155
Title; Associated Form; and OMB
Number: Application for TRICAREProvider Status: Corporation Services
Provider; DD Form X644; OMB Number
0720–0020.
Needs and Uses: The information
collection requirement is necessary to
allow eligible providers to apply for
Corporate Services Provider status
under the TRICARE program.
Affected Public: Business or other for
profit; Not-for-profit institutions.
Annual Burden Hours: 100.
Number of Respondents: 300.
Responses Per Respondent: 1.
Average Burden per Response: 20
minutes.
Frequency: On occasion.
On March 10, 1999, TRICARE
Management Activity (TMA), formerly
known as OCHAMPUS, published a
final rule in the Federal Register (64 FR
11765), creating a fourth class of
TRICARE providers consisting of
freestanding corporations and
foundations that render principally
professional ambulatory or in-home care
and technical diagnostic procedures.
Effective October 1, 2013, the TRICARE
Management Activity is now the
Defense Health Agency (DHA). The
intent of the rule was not to create
additional benefits that ordinarily
would not be covered under TRICARE
if provided by a more traditional
healthcare delivery system, but rather to
allow those services which would
otherwise be allowed except for an
individual provider’s affiliation with a
freestanding corporate facility. The
addition of the corporate class
recognized the current range of
providers within today’s health care
delivery structure, and gave
beneficiaries access to another segment
of the health care delivery industry.
Corporate services providers must be
approved for Medicare payment, or
when Medicare approval status is not
required, be accredited by a qualified
accreditation organization to gain
provider authorization status under
TRICARE. Corporate services providers
must also enter into a participation
agreement which will be sent out as part
of the initial authorization process. The
participation agreement will ensure that
TRICARE-determined allowable
payments, combined with the costshare/
copayment, deductible, and other health
insurance amounts, will be accepted by
the provider as payment in full. The
application for TRICARE-Provider
Status: Corporate Services Provider, will
collect the necessary information to
ensure that the conditions are met for
authorization as a TRICARE corporate
services provider: i.e., the provider (1) is
a corporation or a foundation, but not a
E:\FR\FM\13JAN1.SGM
13JAN1
tkelley on DSK3SPTVN1PROD with NOTICES
2156
Federal Register / Vol. 79, No. 8 / Monday, January 13, 2014 / Notices
professional corporation or professional
association; (2) provides services and
related supplies of a type rendered by
TRICARE individual professional
providers or diagnostic technical
services; (3) is approved for Medicare
payment or, when Medicare approval
status is not required, is accredited by
a qualified accreditation organization;
and (4) has entered into a participation
agreement approved by the Director,
DHA or a designee.
The collected information will be
used by TRICARE contractors to process
claims and verify authorized provider
status. Verification involves collecting
and reviewing copies of the provider’s
licenses, certificates, accreditation
documents, etc. If the criteria are met,
the provider is granted TRICARE
authorization status. The documentation
and information are collected when:
(1) A provider requests permission to
become a TRICARE-authorized
provider; (2) a claim is filed for care
received from a provider who is not
listed on the contractors’ computer
listing of authorized providers; or (3)
when a former TRICARE-authorized
provider requests reinstatement. The
contractors develop the forms used to
gather information based on TRICARE
conditions for participation listed
above. Without the collection of this
information, contractors cannot
determine if the provider meets
TRICARE-authorization requirements
for corporate services providers. If the
contractor is unable to verify that a
provider meets these authorization
requirements, the contractor may not
reimburse either the provider or the
beneficiary for the provider’s health care
services. To reduce the reporting burden
to a minimum, TRICARE has carefully
selected the information requested from
respondents. Only that information
which has been deemed absolutely
essential is being requested. If
necessary, contractors may verify
credentials with Medicare, JCAHO and
other national organizations by
telephone. TRICARE is also
participating with Medicare in the
development of a National Provider
System which will eliminate
duplication of provider certification
data collection among Federal
government agencies. TRICARE
contractors are required to maintain a
computer listing of all providers that
have submitted the appropriate
authorization information and
documentation. To avoid duplicate
inquires, the contractors must search the
computer provider listing before
requesting documentation from
providers. Since the providers affected
VerDate Mar<15>2010
16:40 Jan 10, 2014
Jkt 232001
by this information collection generally
have not previously been eligible to be
authorized providers, TRICARE
contractors will have no information on
file. The providers will have to submit
the information requested on the data
collection form (Application for
TRICARE-Providers Status: Corporate
Services Provider) in order to obtain
provider authorization status under
TRICARE. The information will usually
be collected from each respondent only
once. It is estimated that there will be
approximately 300 applicants per year.
TRICARE will request the provider
authorization documentation and
information when the provider asks to
become TRICARE-authorized or when a
claim is filed for a new provider’s
services. If after a provider has been
authorized by a contractor, no claims
are filed during two-year period of time,
the provider’s information will be
placed in the inactive file. To reactivate
a file, the provider must verify that the
information is still correct, or supply
new or changed information. The total
annual reporting burden is estimated to
be approximately 100 hours
(approximately 300 respondents with 20
minutes to complete the form).
Dated: January 7, 2014.
Aaron Siegel,
Alternate OSD Federal Register Liaison
Officer, Department of Defense.
[FR Doc. 2014–00296 Filed 1–10–14; 8:45 am]
BILLING CODE 5001–06–P
Department of the Army
Notice of Availability for Exclusive,
Non-Exclusive, or Partially-Exclusive
Licensing of an Invention Concerning
Anti-Filovirus Therapeutics
Department of the Army, DoD.
Notice.
AGENCY:
Announcement is made of the
availability for licensing of the
invention set forth in U.S. Provisional
Patent Application Serial No. 61/
761,942, entitled ‘‘Anti-Filovirus
Therapeutics,’’ filed on February 7,
2013. The United States Government, as
represented by the Secretary of the
Army, has rights to this invention.
ADDRESSES: Commander, U.S. Army
Medical Research and Materiel
Command, ATTN: Command Judge
Advocate, MCMR–JA, 504 Scott Street,
Fort Detrick, Frederick, MD 21702–
5012.
FOR FURTHER INFORMATION CONTACT: For
patent issues, Ms. Elizabeth Arwine,
Patent Attorney, (301) 619–7808. For
SUMMARY:
PO 00000
Frm 00010
Fmt 4703
Sfmt 4703
Brenda S. Bowen,
Army Federal Register Liaison Officer.
[FR Doc. 2014–00290 Filed 1–10–14; 8:45 am]
BILLING CODE 3710–08–P
DEPARTMENT OF DEFENSE
Department of the Army
Notice of Availability for Exclusive,
Non-Exclusive, or Partially-Exclusive
Licensing of an Invention Concerning
Imidazenil, or a Combination of
Imidazenil and [+]-Huperzine A and/or
[-]-Huperzine A for Protection Against
and/or Treatment of Seizure/Status
Epilepticus and Neuropathology
Following Nerve Agent or
Organophosphate Exposure,
Compositions and Kits
Department of the Army, DoD.
ACTION: Notice.
AGENCY:
Announcement is made of the
availability for licensing of the
invention set forth in U.S. Provisional
Patent Application Serial No. 61/
726,753, entitled ‘‘Imidazenil, or a
Combination of Imidazenil and [+]Huperzine A and/or [-]-Huperzine A for
Protection Against and/or Treatment of
Seizure/Status Epilepticus and
Neuropathology Following Nerve Agent
or Organophosphate Exposure,
Compositions and Kits,’’ filed on
November 15, 2012. The United States
Government, as represented by the
Secretary of the Army, has rights to this
invention.
ADDRESSES: Commander, U.S. Army
Medical Research and Materiel
Command, ATTN: Command Judge
Advocate, MCMR–JA, 504 Scott Street,
Fort Detrick, Frederick, MD 21702–
5012.
SUMMARY:
DEPARTMENT OF DEFENSE
ACTION:
licensing issues, Dr. Paul Mele, Office of
Research and Technology Applications
(ORTA), (301) 619–6664, both at telefax
(301) 619–5034.
SUPPLEMENTARY INFORMATION: The
invention relates to an antisense
oligonucleotide directed to a mRNA
encoding a mammalian Niemann-Pick
C1 (NPC1) receptor, and combinations
thereof and compositions comprising
such are provided. Also provided are
methods of treating or reducing filovirus
infection of a subject.
For
patent issues, Ms. Elizabeth Arwine,
Patent Attorney, (301) 619–7808. For
licensing issues, Dr. Paul Mele, Office of
Research and Technology Applications
(ORTA), (301) 619–6664, both at telefax
(301) 619–5034.
FOR FURTHER INFORMATION CONTACT:
E:\FR\FM\13JAN1.SGM
13JAN1
Agencies
[Federal Register Volume 79, Number 8 (Monday, January 13, 2014)]
[Notices]
[Pages 2155-2156]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2014-00296]
-----------------------------------------------------------------------
DEPARTMENT OF DEFENSE
Office of the Secretary
[Docket ID DoD-2014-HA-0004]
Proposed Collection; Comment Request
AGENCY: Office of the Assistant Secretary of Defense for Health
Affairs, DoD.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: In compliance with Section 3506(c)(2)(A) of the Paperwork
Reduction Act of 1995, the Office of the Assistant Secretary of Defense
for Health Affairs announces a proposed public information collection
and seeks public comment on the provisions thereof. Comments are
invited on: (a) Whether the proposed collection of information is
necessary for the proper performance of the functions of the agency,
including whether the information shall have practical utility; (b) the
accuracy of the agency's estimate of the burden of the proposed
information collection; (c) ways to enhance the quality, utility, and
clarity of the information to be collected; and (d) ways to minimize
the burden of the information collection on respondents, including
through the use of automated collection techniques or other forms of
information technology.
DATES: Consideration will be given to all comments received by March
14, 2014.
ADDRESSES: You may submit comments, identified by docket number and
title, by any of the following methods:
Federal eRulemaking Portal: https://www.regulations.gov.
Follow the instructions for submitting comments.
Mail: Federal Docket Management System Office, 4800 Mark
Center Drive, East Tower, Suite 02G09, Alexandria, VA 22350-3100.
Instructions: All submissions received must include the agency
name, docket number and title for this Federal Register document. The
general policy for comments and other submissions from members of the
public is to make these submissions available for public viewing on the
Internet at https://www.regulations.gov as they are received without
change, including any personal identifiers or contact information.
Any associated form(s) for this collection may be located within
this same electronic docket and downloaded for review/testing. Follow
the instructions at https://www.regulations.gov for submitting comments.
Please submit comments on any given form identified by docket number,
form number, and title.
FOR FURTHER INFORMATION CONTACT: To request more information on this
proposed information collection or to obtain a copy of the proposal and
associated collection instruments, please write to the Defense Health
Agency, Medical Benefits and Reimbursement Systems, 16401 East
Centretech Parkway, ATTN: Elan Green, Aurora, CO 80011-9043, or call
Defense Health Agency, Medical Benefits and Reimbursement Office, at
(303) 676-3907.
SUPPLEMENTARY INFORMATION:
Title; Associated Form; and OMB Number: Application for TRICARE-
Provider Status: Corporation Services Provider; DD Form X644; OMB
Number 0720-0020.
Needs and Uses: The information collection requirement is necessary
to allow eligible providers to apply for Corporate Services Provider
status under the TRICARE program.
Affected Public: Business or other for profit; Not-for-profit
institutions.
Annual Burden Hours: 100.
Number of Respondents: 300.
Responses Per Respondent: 1.
Average Burden per Response: 20 minutes.
Frequency: On occasion.
On March 10, 1999, TRICARE Management Activity (TMA), formerly
known as OCHAMPUS, published a final rule in the Federal Register (64
FR 11765), creating a fourth class of TRICARE providers consisting of
freestanding corporations and foundations that render principally
professional ambulatory or in-home care and technical diagnostic
procedures. Effective October 1, 2013, the TRICARE Management Activity
is now the Defense Health Agency (DHA). The intent of the rule was not
to create additional benefits that ordinarily would not be covered
under TRICARE if provided by a more traditional healthcare delivery
system, but rather to allow those services which would otherwise be
allowed except for an individual provider's affiliation with a
freestanding corporate facility. The addition of the corporate class
recognized the current range of providers within today's health care
delivery structure, and gave beneficiaries access to another segment of
the health care delivery industry. Corporate services providers must be
approved for Medicare payment, or when Medicare approval status is not
required, be accredited by a qualified accreditation organization to
gain provider authorization status under TRICARE. Corporate services
providers must also enter into a participation agreement which will be
sent out as part of the initial authorization process. The
participation agreement will ensure that TRICARE-determined allowable
payments, combined with the costshare/copayment, deductible, and other
health insurance amounts, will be accepted by the provider as payment
in full. The application for TRICARE-Provider Status: Corporate
Services Provider, will collect the necessary information to ensure
that the conditions are met for authorization as a TRICARE corporate
services provider: i.e., the provider (1) is a corporation or a
foundation, but not a
[[Page 2156]]
professional corporation or professional association; (2) provides
services and related supplies of a type rendered by TRICARE individual
professional providers or diagnostic technical services; (3) is
approved for Medicare payment or, when Medicare approval status is not
required, is accredited by a qualified accreditation organization; and
(4) has entered into a participation agreement approved by the
Director, DHA or a designee.
The collected information will be used by TRICARE contractors to
process claims and verify authorized provider status. Verification
involves collecting and reviewing copies of the provider's licenses,
certificates, accreditation documents, etc. If the criteria are met,
the provider is granted TRICARE authorization status. The documentation
and information are collected when: (1) A provider requests permission
to become a TRICARE-authorized provider; (2) a claim is filed for care
received from a provider who is not listed on the contractors' computer
listing of authorized providers; or (3) when a former TRICARE-
authorized provider requests reinstatement. The contractors develop the
forms used to gather information based on TRICARE conditions for
participation listed above. Without the collection of this information,
contractors cannot determine if the provider meets TRICARE-
authorization requirements for corporate services providers. If the
contractor is unable to verify that a provider meets these
authorization requirements, the contractor may not reimburse either the
provider or the beneficiary for the provider's health care services. To
reduce the reporting burden to a minimum, TRICARE has carefully
selected the information requested from respondents. Only that
information which has been deemed absolutely essential is being
requested. If necessary, contractors may verify credentials with
Medicare, JCAHO and other national organizations by telephone. TRICARE
is also participating with Medicare in the development of a National
Provider System which will eliminate duplication of provider
certification data collection among Federal government agencies.
TRICARE contractors are required to maintain a computer listing of all
providers that have submitted the appropriate authorization information
and documentation. To avoid duplicate inquires, the contractors must
search the computer provider listing before requesting documentation
from providers. Since the providers affected by this information
collection generally have not previously been eligible to be authorized
providers, TRICARE contractors will have no information on file. The
providers will have to submit the information requested on the data
collection form (Application for TRICARE-Providers Status: Corporate
Services Provider) in order to obtain provider authorization status
under TRICARE. The information will usually be collected from each
respondent only once. It is estimated that there will be approximately
300 applicants per year. TRICARE will request the provider
authorization documentation and information when the provider asks to
become TRICARE-authorized or when a claim is filed for a new provider's
services. If after a provider has been authorized by a contractor, no
claims are filed during two-year period of time, the provider's
information will be placed in the inactive file. To reactivate a file,
the provider must verify that the information is still correct, or
supply new or changed information. The total annual reporting burden is
estimated to be approximately 100 hours (approximately 300 respondents
with 20 minutes to complete the form).
Dated: January 7, 2014.
Aaron Siegel,
Alternate OSD Federal Register Liaison Officer, Department of Defense.
[FR Doc. 2014-00296 Filed 1-10-14; 8:45 am]
BILLING CODE 5001-06-P