Proposed Collection, Comment Request, 31813-31814 [07-2844]

Download as PDF 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
This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.