Proposed Collection, Comment Request, 31813-31814 [07-2844]
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Federal Register / Vol. 72, No. 110 / Friday, June 8, 2007 / Notices
SUMMARY: The Committee for the
Implementation of Textile Agreements
(CITA) has determined that certain
synthetic staple fibers, as specified
below, are not available in commercial
quantities in a timely manner in the
CAFTA-DR region. The product will be
added to the list in Annex 3.25 of the
CAFTA-DR Agreement in unrestricted
quantities.
FOR FURTHER INFORMATION CONTACT:
Richard Stetson, Office of Textiles and
Apparel, U.S. Department of Commerce,
(202) 482 2582.
FOR FURTHER INFORMATION ONLINE: https://web.ita.doc.gov/tacgi/
CaftaReqTrack.nsf.Reference number:
22.2007.05.02.Fiber.TextilesCapuano,
SA
SUPPLEMENTARYINFORMATION:
Authority: Section 203(o)(4) of the
Dominican Republic-Central America-United
States Free Trade Agreement Implementation
Act (CAFTA-DR Act); the Statement of
Administrative Action (SAA), accompanying
the CAFTA-DR Act; Presidential
Proclamations 7987 (February 28, 2006) and
7996 (March 31, 2006).
pwalker on PROD1PC71 with NOTICES
BACKGROUND:
The CAFTA-DR Agreement provides a
list in Annex 3.25 for fabrics, yarns, and
fibers that the Parties to the CAFTA-DR
Agreement have determined are not
available in commercial quantities in a
timely manner in the territory of any
Party. Articles that otherwise meet the
rule of origin to qualify for preferential
treatment are not disqualified because
they contain one of the products on the
Annex 3.25 list.
The CAFTA-DR Agreement provides
that this list may be modified pursuant
to Article 3.25(4)-(5), when the
President of the United States
determines that a fabric, yarn, or fiber is
not available in commercial quantities
in a timely manner in the territory of
any Party. The CAFTA-DR Act states
that the President will make a
determination on whether additional
fabrics, yarns, and fibers are available in
commercial quantities in a timely
manner in the territory of any Party.
The CAFTA-DR Act requires the
President to establish procedures
governing the submission of a request
and providing opportunity for interested
entities to submit comments and
supporting evidence before a
commercial availability determination is
made. In Presidential Proclamations
7987 and 7996, the President delegated
to CITA the authority under section
203(o)(4) of the CAFTA-DR Act for
modifying the Annex 3.25 list. On
March 21, 2007, CITA published final
procedures it would follow in
VerDate Aug<31>2005
19:26 Jun 07, 2007
Jkt 211001
considering requests to modify the
Annex 3.25 list (72 FR 13256).
On May 2, 2007, the Chairman of
CITA received a request from Textiles
Capuano, S.A. for certain synthetic
staple fibers of the specifications
detailed below. On May 4, 2007, CITA
notified interested parties of, and posted
on its website, the accepted request and
requested that any interested entity
provide, by May 16, 2007, a response
advising of its objection to the request
or its ability to supply the subject
product, and rebuttals to responses by
May 22, 2007.
No interested entity filed a response
advising of its objection to the request
or its ability to supply the subject
product.
In accordance with Section
203(o)(4)(C)(iii)(II) of the CAFTA-DR
Act, and its procedures, as no interested
entity submitted a response objecting to
the request or expressing an ability to
supply the subject product, CITA has
determined to add the specified fibers to
the list in Annex 3.25 of the CAFTA-DR
Agreement.
The subject fibers are added to the list
in Annex 3.25 of the CAFTA-DR
Agreement in unrestricted quantities. A
revised list has been published on-line.
Specifications:
Product:
HTS Subheading:
Synthetic staple fiber,
not carded, combed
or otherwise processed for spinning of
acrylic or modacrylic
(Raw White Bright or
Semi Dull - Acrylic
Short Staple Fiber,
1.3 DTEX to 1.5
DTEX Bright 38 40mm)
5503.30.00
Philip J. Martello,
Acting Chairman, Committee for the
Implementation of Textile Agreements.
[FR Doc. E7–11139 Filed 6–7–07; 8:45 am]
BILLING CODE 3510–DS
DEPARTMENT OF DEFENSE
Office of the Secretary
[No. DoD–2007–HA–0030]
Proposed Collection, Comment
Request
Office of the Assistant
Secretary of Defense for Health Affairs,
DoD.
ACTION: Notice.
AGENCY:
In accordance with section 3506(c) of
the Paperwork Reduction Act of 1995,
PO 00000
Frm 00019
Fmt 4703
Sfmt 4703
31813
the Office of the Assistant Secretary of
Defense for Health Affairs announces
the proposed extension of a public
information collection and seeks public
comment on the provisions thereof.
Comments are invited on: (a) Whether
the proposed extension of 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 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: Considerations will be given to
all comments received by August 7,
2007.
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, 1160 Defense Pentagon,
Washington, DC 20301–1160.
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.
FOR FURTHER INFORMATION CONTACT: To
request more information on this
proposed information collection, please
write to the TRICARE Management
Activity, Medical Benefits and
Reimbursement System, 16401 E.
Centretech Pkwy, Attn: Ann Fazzini,
Aurora, CO 80011–9066, or call
TRICARE Management Activity,
Medical Benefits and Reimbursement
Systems at (303) 676–3803.
Title and OMB Number: Diagnosis
Related Groups (DRG) Reimbursement
(Two Parts); OMB Control Number
0720–0017.
Needs and Uses: The TRICARE/
CHAMPUS contractors will use the
information collected to reimburse
hospitals for TRICARE/CHAMPUS share
of capital and direct medical education
costs. Respondents are institutional
providers.
Affected Public: Business or other-forprofit.
E:\FR\FM\08JNN1.SGM
08JNN1
31814
Federal Register / Vol. 72, No. 110 / Friday, June 8, 2007 / Notices
and misrepresentation may be subject to
penalties.
Summary of Information Collection
pwalker on PROD1PC71 with NOTICES
Annual Burden Hours: 8,400.
Number of Respondents: 5,600.
Responses per Respondent: 1.
Average Burden per Response: 90
minutes.
Frequency: On occasion.
SUPPLEMENTARY INFORMATION:
BILLING CODE 5001–06–M
Dated: June 1, 2007.
Patricia L. Toppings,
Alternate OSD Federal Register Liaison
Officer, Department of Defense.
[FR Doc. 07–2844 Filed 6–7–07; 8:45 am]
The Department of Defense
Authorization Act, 1984, Pub. L. 98–94
amended Title 10, section 1079(j)(2)(A)
of the U.S.C. and provided the Civilian
Health and Medical Program of the
Uniform Services (CHAMPUS) with the
statutory authority to reimburse
institutional providers based on
diagnosis-related groups (DRGs).
Institutional providers in the
CHAMPUS DRG-based payment system,
except for children’s hospitals (whose
capital and direct medical education
costs are incorporated in the children’s
hospital differential), who want to be
reimbursed for allowed capital and
direct medical education costs must
submit a request for payment to the
TRICARE/CHAMPUS contractor. The
request allows TRICARE to collect the
information necessary to properly
reimburse hospitals for its share of these
costs. The information can be submitted
in any form, most likely in the form of
a letter. The contractor will calculate the
TRICARE/CHAMPUS share of capital
and direct medical educations costs and
make a lump-sum payment to the
hospital.
The TRICARE/CHAMPUS DRG-based
payment system is modeled on the
Medicare Prospective Payment System
(PPS) and was implemented on October
1, 1987. Initially, under 42 CFR 412.46
of the Medicare regulations, physicians
were required to sign attestation and
acknowledgment statements. These
requirements were implemented to
ensure a means of holding hospitals and
physicians accountable for the
information they submit on the
Medicare claim forms. Being modeled
on the Medicare PPS, CHAMPUS also
adopted these requirements. The
physicians attestation and physician
acknowledgment required by Medicare
under 42 CFR 412.46 are also required
for CHAMPUS as a condition for
payment and may be satisfied by the
same statements as required for
Medicare, with substitution or addition
of ‘‘CHAMPUS’’ when the word
‘‘Medicare’’ is used. Physicians sign a
physician acknowledgment, maintained
by the institution, at the time the
physician is granted admitting
privileges. This acknowledgment
indicates the physician understands the
importance of a correct medical record,
VerDate Aug<31>2005
18:14 Jun 07, 2007
Jkt 211001
Office of the Secretary
[Docket No. DOD–2007–OS–0061]
Proposed Collection: Comment
Request
Department of Defense, Office
of the Under Secretary of Defense for
Acquisition, Technology, and Logistics/
Defense Technical Information Center
(DTIC).
ACTION: Notice.
AGENCY:
In compliance with Section
3506(C)(2)(A) of the Paperwork
Reduction Act of 1995, the Office of the
Under Secretary of Defense for
Acquisition, Technology, and Logistics/
Defense Technical Information Center
(DTIC) announces the proposed
extension of the currently approved
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.
(d) Ways to minimize the burden of
the information collection on
respondents, including the use of
automated collection techniques or
other forms of information technology.
DATES: Consideration will be given to all
comments received by August 7, 2007.
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, 1160 Defense Pentagon,
Washington, DC 20301–1160.
• 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
Frm 00020
Fmt 4703
To
request further information about this
proposed information collection, or to
obtain a copy of the proposal and the
associated collection instrument, please
write or send an e-mail to the DTIC–BC
Registration Team, Defense Technical
Information Center, 8725 John J.
Kingman Road, Suite 0944, Fort Belvoir,
VA 22060–6218, or e-mail Ms. Kerry
Christensen: kchriste@dtic.mil. Ms.
Christensen may be telephoned at: (703)
767–8247.
Title, Form, and OMB Number:
Registration for Scientific and Technical
Information Services; DD Form 1540;
OMB Control Number 0704–0264.
Needs and Uses: The data that the
Defense Technical Information Center
handles is controlled, because of either
distribution limitations or security
classification. For this reason, all
potential users are required to register
for service. DoD Instruction 3200.14,
Principles and Operational Parameters
of the DoD Scientific and Technical
Information Program, mandates the
registration procedure. Federal
Government agencies and their
contractors are required to complete the
DD Form 1540, Registration for
Scientific and Technical Information
Services. The contractor community
completes a separate DD Form 1540 for
each contract or grant, and registration
is valid until the contract expires.
Affected Public: Business or other-forprofit, Federal Government, and State,
local, or tribal government.
Annual Burden Hours: 1,667.
Number of Annual Respondents:
10,000.
Annual Responses to Respondent:
10,000.
Average Burden per Response: 10
minutes.
Frequency: On occasion.
FOR FURTHER INFORMATION CONTACT:
DEPARTMENT OF DEFENSE
PO 00000
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.
Sfmt 4703
SUPPLEMENTARY INFORMATION:
Summary of Information Collection
The DD Form 1540 serves as a
registration tool for Federal Government
agencies and their contractors to access
DTIC services. Potential users
registering for services are required to
obtain certification from a designated
approving official. Collected
information is verified by DTIC’s
Marketing and Registration Division.
E:\FR\FM\08JNN1.SGM
08JNN1
Agencies
[Federal Register Volume 72, Number 110 (Friday, June 8, 2007)]
[Notices]
[Pages 31813-31814]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 07-2844]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF DEFENSE
Office of the Secretary
[No. DoD-2007-HA-0030]
Proposed Collection, Comment Request
AGENCY: Office of the Assistant Secretary of Defense for Health
Affairs, DoD.
ACTION: Notice.
-----------------------------------------------------------------------
In accordance with section 3506(c) of the Paperwork Reduction Act
of 1995, the Office of the Assistant Secretary of Defense for Health
Affairs announces the proposed extension of a public information
collection and seeks public comment on the provisions thereof. Comments
are invited on: (a) Whether the proposed extension of 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
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: Considerations will be given to all comments received by August
7, 2007.
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, 1160
Defense Pentagon, Washington, DC 20301-1160.
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.
FOR FURTHER INFORMATION CONTACT: To request more information on this
proposed information collection, please write to the TRICARE Management
Activity, Medical Benefits and Reimbursement System, 16401 E.
Centretech Pkwy, Attn: Ann Fazzini, Aurora, CO 80011-9066, or call
TRICARE Management Activity, Medical Benefits and Reimbursement Systems
at (303) 676-3803.
Title and OMB Number: Diagnosis Related Groups (DRG) Reimbursement
(Two Parts); OMB Control Number 0720-0017.
Needs and Uses: The TRICARE/CHAMPUS contractors will use the
information collected to reimburse hospitals for TRICARE/CHAMPUS share
of capital and direct medical education costs. Respondents are
institutional providers.
Affected Public: Business or other-for-profit.
[[Page 31814]]
Annual Burden Hours: 8,400.
Number of Respondents: 5,600.
Responses per Respondent: 1.
Average Burden per Response: 90 minutes.
Frequency: On occasion.
SUPPLEMENTARY INFORMATION:
Summary of Information Collection
The Department of Defense Authorization Act, 1984, Pub. L. 98-94
amended Title 10, section 1079(j)(2)(A) of the U.S.C. and provided the
Civilian Health and Medical Program of the Uniform Services (CHAMPUS)
with the statutory authority to reimburse institutional providers based
on diagnosis-related groups (DRGs). Institutional providers in the
CHAMPUS DRG-based payment system, except for children's hospitals
(whose capital and direct medical education costs are incorporated in
the children's hospital differential), who want to be reimbursed for
allowed capital and direct medical education costs must submit a
request for payment to the TRICARE/CHAMPUS contractor. The request
allows TRICARE to collect the information necessary to properly
reimburse hospitals for its share of these costs. The information can
be submitted in any form, most likely in the form of a letter. The
contractor will calculate the TRICARE/CHAMPUS share of capital and
direct medical educations costs and make a lump-sum payment to the
hospital.
The TRICARE/CHAMPUS DRG-based payment system is modeled on the
Medicare Prospective Payment System (PPS) and was implemented on
October 1, 1987. Initially, under 42 CFR 412.46 of the Medicare
regulations, physicians were required to sign attestation and
acknowledgment statements. These requirements were implemented to
ensure a means of holding hospitals and physicians accountable for the
information they submit on the Medicare claim forms. Being modeled on
the Medicare PPS, CHAMPUS also adopted these requirements. The
physicians attestation and physician acknowledgment required by
Medicare under 42 CFR 412.46 are also required for CHAMPUS as a
condition for payment and may be satisfied by the same statements as
required for Medicare, with substitution or addition of ``CHAMPUS''
when the word ``Medicare'' is used. Physicians sign a physician
acknowledgment, maintained by the institution, at the time the
physician is granted admitting privileges. This acknowledgment
indicates the physician understands the importance of a correct medical
record, and misrepresentation may be subject to penalties.
Dated: June 1, 2007.
Patricia L. Toppings,
Alternate OSD Federal Register Liaison Officer, Department of Defense.
[FR Doc. 07-2844 Filed 6-7-07; 8:45 am]
BILLING CODE 5001-06-M