Agency Information Collection Activities: Proposed Collection; Comment Request, 17887-17888 [E6-4947]

Download as PDF Federal Register / Vol. 71, No. 67 / Friday, April 7, 2006 / Notices information that is required in the body of the application. Be sure to crossreference all tables and attachments located in the appendices to the appropriate text in the application. Carefully proofread the application. Misspellings and grammatical errors will impede reviewers in understanding the application. Be sure pages are numbered (including appendices) and that page limits are followed. Limit the use of abbreviations and acronyms, and define each one at its first use and periodically throughout application. Dated: March 31, 2006. Mary Lou Valdez, Deputy Director for Policy, Office of Global Health Affairs. [FR Doc. E6–5047 Filed 4–6–06; 8:45 am] BILLING CODE 4150–38–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention wwhite on PROD1PC61 with NOTICES Amendment of February 4, 2004, Order To Embargo Birds and Bird Products Imported From Jordan SUMMARY: On February 4, 2004, the Centers for Disease Control and Prevention (CDC) within the U.S. Department of Health and Human Services issued an order to ban immediately the import of all birds (Class: Aves) from specified countries, subject to limited exemptions for returning pet birds of U.S. origin and certain processed bird-derived products. HHS/CDC took this step because birds from these countries potentially can infect humans with avian influenza (influenza A/ [H5N1]). The February 4, 2004, order complemented a similar action taken at the same time by the Animal and Plant Health Inspection Service (APHIS) within the U.S. Department of Agriculture (USDA). On March 10, 2004, HHS/CDC lifted the embargo of birds and bird products from the Hong Kong Special Administrative Region (HKSAR) because of the documented publichealth and animal health measures taken by Hong Kong officials to prevent spread of the outbreak within the HKSAR, and the absence of highly pathogenic avian influenza H5N1 cases in Hong Kong’s domestic and wild bird populations. USDA/APHIS took a similar action. On September 28, 2004, HHS/CDC extended the embargo on birds and bird products to include Malaysia because of the documented cases of highly pathogenic avian influenza A H5N1 in poultry in VerDate Aug<31>2005 19:13 Apr 06, 2006 Jkt 208001 Malaysia. On July 20, 2005, USDA/ APHIS adopted as a final rule the interim rule that became effective on February 4, 2004, which amended its regulations to prohibit or restrict the importation of birds, poultry, and unprocessed birds and poultry products from regions that have reported the presence of highly pathogenic avian influenza H5N1 in poultry. (See 70 FR 41608 [July 20, 2005].) As the United Nations Food and Agriculture Organization and the World Organization for Animal Health (OIE) have confirmed additional cases of highly pathogenic avian influenza (H5N1), USDA/APHIS has added additional countries to its ban. Because of the documentation of highly pathogenic avian influenza H5N1 in poultry, HHS/CDC added the following countries to its embargo: Kazakhstan, Romania, Russia, Turkey, and Ukraine on December 29, 2005; Nigeria on February 8, 2006; Indian on February 22, 2006; Egypt on February 27, 2006; Niger on March 2, 2006; Albania, Azerbaijan, Cameroon, and Burma (Myanmar) on March 15, 2006; Israel on March 20, 2006; and Afghanistan on March 21, 2006. On March 23, 2006, OIE reported confirmation of highly pathogenic avian influenza H5N1 in poultry in Jordan. At this time, HHS/CDC is adding Jordan to its current embargo. This action is effective on March 29, 2006, and will remain in effect until further notice. SUPPLEMENTARY INFORMATION: Background On March 23, 2006, OIE reported confirmation of highly pathegenic avian influenza H5N1 in chickens and turkeys in Kofranja, Jordan. Introduction of birds infected with highly pathogenic avian influenza H5N1 into the United States could lead to outbreaks of disease among birds and among the human population, a significant public health threat. Banning the importation of all avian species from affected countries is an effective means of limiting this threat. HHS/CDC is therefore taking this action to reduce the likelihood of introduction or spread of influenza A H5N1 into the United States. Immediate Action Therefore, pursuant to 42 CFR 71.32(b), HHS/CDC is amending the February 4, 2004, order to add Jordan to the list of countries subject to the order’s embargo of birds and products derived from birds. All other portions of the February 4, 2004, order, as further amended on March 10, 2004, September 28, 2004, December 29, 2005, February PO 00000 Frm 00083 Fmt 4703 Sfmt 4703 17887 8, 2006, February 22, 2006, February 27, 2006, March 2, 2006, March 25, 2006, March 20, 2006, and March 21, 2006 shall remain in effect until further notice. Dated: March 30, 2006. Julie Louise Gerberding, Director, Centers for Disease Control and Prevention, U.S. Department of Health and Human Services. [FR Doc. 06–3273 Filed 4–6–06; 8:45 am] BILLING CODE 4163–18–M DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Medicare & Medicaid Services [Document Identifier: CMS–R–52 and CMS– R–194] Agency Information Collection Activities: Proposed Collection; Comment Request Centers for Medicare & Medicaid Services. In compliance with the requirement of section 3506(c)(2)(A) of the Paperwork Reduction Act of 1995, the Centers for Medicare & Medicaid Services (CMS) is publishing the following summary of proposed collections for public comment. Interested persons are invited to send comments regarding this burden estimate 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 be collected; and (4) the use of automated collection techniques or other forms of information technology to minimize the information collection burden. 1. Type of Information Collection Request: Extension of a currently approved collection; Title of Information Collection: Conditions for Coverage of Suppliers of End Stage Renal Disease (ESRD) Services and Supporting Regulations Contained in 42 CFR 405.2100–405.2171; Use: The requirements associated with the Medicare and Medicaid Conditions for Coverage for Suppliers of ESRD Services fall into two categories: record keeping requirements and reporting requirements. With regard to the recordkeeping requirements, CMS uses these conditions for coverage to certify health care facilities that want to participate in the Medicare or Medicaid AGENCY: E:\FR\FM\07APN1.SGM 07APN1 wwhite on PROD1PC61 with NOTICES 17888 Federal Register / Vol. 71, No. 67 / Friday, April 7, 2006 / Notices programs. These record keeping requirements are no different than other conditions for coverage in that they reflect comparable standards developed by industry organizations such as the Renal Physicians Association, American Society of Transplant Surgeons, and the National Association of Patients on Hemodialysis and Transplantation. With respect to reporting requirements, the information is needed to assess and ensure proper distribution and effective utilization of ESRD treatment resources while maintaining or improving quality of care. It is CMS’s responsibility to closely monitor ESRD service utilization to prevent over-expansion of facilities and resultant under-utilization.; Form Number: CMS–R–52 (OMB#: 0938– 0386); Frequency: Recordkeeping and Reporting—Annually; Affected Public: Business or other for-profit and Federal government; Number of Respondents: 4,757; Total Annual Responses: 4,757; Total Annual Hours: 160,702. 2. Type of Information Collection Request: Extension of a currently approved collection; Title of Information Collection: Medicare Disproportionate Share Adjustment Procedures and Criteria and Supporting Regulations in 42 CFR 412.106; Use: A hospital’s disproportionate share adjustment is determined by its fiscal intermediary (FI) using a combination of Medicare Part A and Supplemental Security Income data provided by CMS, and Medicaid data calculated from the hospital’s cost report. The data provided through these calculations are then compared to the qualifying criteria located in 42 CFR 412.106 to determine the final adjustment. If these calculations, based on the Federal fiscal year, do not allow the hospital to qualify for a disproportionate share adjustment, the hospital may request that the calculations be performed using its cost reporting period.; Form Number: CMS– R–194 (OMB#: 0938–0691); Frequency: Recordkeeping and Reporting—On occasion; Affected Public: Business or other for-profit and Not-for-profit institutions; Number of Respondents: 100; Total Annual Responses: 100; Total Annual Hours: 100. To obtain copies of the supporting statement and any related forms for the proposed paperwork collections referenced above, access CMS’ Web site address at https://www.cms.hhs.gov/ PaperworkReductionActof1995, or Email your request, including your address, phone number, OMB number, and CMS document identifier, to Paperwork@cms.hhs.gov, or call the Reports Clearance Office on (410) 786– 1326. VerDate Aug<31>2005 19:13 Apr 06, 2006 Jkt 208001 To be assured consideration, comments and recommendations for the proposed information collections must be received at the address below, no later than 5 p.m. on June 6, 2006. CMS, Office of Strategic Operations and Regulatory Affairs, Division of Regulations Development—B, Attention: William N. Parham, III, Room C4–26– 05, 7500 Security Boulevard, Baltimore, Maryland 21244–1850. Dated: March 30, 2006. Michelle Shortt, Director, Regulations Development Group, Office of Strategic Operations and Regulatory Affairs. [FR Doc. E6–4947 Filed 4–6–06; 8:45 am] BILLING CODE 4120–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Medicare & Medicaid Services [CMS–1481–N] Medicare Program; Emergency Medical Treatment and Labor Act (EMTALA) Technical Advisory Group (TAG) Meeting—May 1 Through May 2, 2006 Centers for Medicare & Medicaid Services (CMS), HHS. ACTION: Notice of meeting. AGENCY: SUMMARY: In accordance with section 10(a) of the Federal Advisory Committee Act (FACA) (5 U.S.C. Appendix 2), this notice announces the fourth meeting of the Emergency Medical Treatment and Labor Act (EMTALA) Technical Advisory Group (TAG). The purpose of the EMTALA TAG is to review regulations affecting hospital and physician responsibilities under EMTALA to individuals who come to a hospital seeking examination or treatment for medical conditions. The primary purpose of the fourth meeting is to enable the EMTALA TAG to hear additional testimony and further consider written responses from medical societies and other organizations on specific issues considered by the TAG at previous meetings. However, the public is permitted to attend this meeting and, to the extent that time permits and at the discretion of the Chairperson, the EMTALA TAG may hear comments from the floor. DATES: Meeting Date: The meetings of the EMTALA TAG announced in this notice are as follows: Monday, May 1, 2006, 9 a.m. to 5 p.m. e.s.t. Tuesday, May 2, 2006, 9 a.m. to 5 p.m. e.s.t. PO 00000 Frm 00084 Fmt 4703 Sfmt 4703 Registration Deadline: All individuals must register in order to attend this meeting. Individuals who wish to attend the meeting but do not wish to present testimony must register by April 24, 2006. Individuals who wish to attend the meeting and to present their testimony must register by April 10, 2006 and must submit copies of their testimony in writing by April 17, 2006. See Section IV for more detailed registration instructions. Comment Deadline: Written comments/statements to be presented to the EMTALA TAG must be received by April 17, 2006. Special Accommodations: Individuals requiring sign-language interpretation or other special accommodations should send a request for these services to Eric Ruiz by 5 p.m. on April 17, 2006 at the address listed below. ADDRESSES: Meeting Address: The EMTALA TAG meeting will be held in Room 800 of the Hubert Humphrey Building, 200 Independence Avenue, SW., Washington, DC 20001. Mailing and E-mail Addresses for Inquiries or Comments: Inquiries or comments regarding this meeting may be sent to—Eric Ruiz, Division of Acute Care, Centers for Medicare & Medicaid Services, Mail Stop C4–08–06, 7500 Security Boulevard, Baltimore, MD 21244–1850. Inquiries or comments may also be emailed to Eric.Ruiz@cms.hhs.gov or EMTALATAG@cms.hhs.gov. Web Site Address for Additional Information: For additional information on the EMTALA TAG meeting agenda topics, updated activities, and to obtain Charter copies, please search our Internet Web site at (https:// www.cms.hhs.gov/faca/ 07_emtalatag.asp). FOR FURTHER INFORMATION CONTACT: Eric Ruiz, (410) 786–0247. George Morey, (410) 786–4653. Press inquiries are handled through the CMS Press Office at (202) 690–6145. SUPPLEMENTARY INFORMATION: I. Background Sections 1866(a)(1)(I), 1866(a)(1)(N), and 1867 of the Social Security Act (the Act) impose specific obligations on Medicare-participating hospitals that offer emergency services. These obligations concern individuals who come to a hospital emergency department and request or have a request made on their behalf for examination or treatment for a medical condition. The Emergency Medical Treatment and Labor Act (EMTALA) applies to all these individuals, regardless of whether or not they are E:\FR\FM\07APN1.SGM 07APN1

Agencies

[Federal Register Volume 71, Number 67 (Friday, April 7, 2006)]
[Notices]
[Pages 17887-17888]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E6-4947]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Centers for Medicare & Medicaid Services

[Document Identifier: CMS-R-52 and CMS-R-194]


Agency Information Collection Activities: Proposed Collection; 
Comment Request

AGENCY: Centers for Medicare & Medicaid Services.
    In compliance with the requirement of section 3506(c)(2)(A) of the 
Paperwork Reduction Act of 1995, the Centers for Medicare & Medicaid 
Services (CMS) is publishing the following summary of proposed 
collections for public comment. Interested persons are invited to send 
comments regarding this burden estimate 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 be collected; and (4) the use of 
automated collection techniques or other forms of information 
technology to minimize the information collection burden.
    1. Type of Information Collection Request: Extension of a currently 
approved collection; Title of Information Collection: Conditions for 
Coverage of Suppliers of End Stage Renal Disease (ESRD) Services and 
Supporting Regulations Contained in 42 CFR 405.2100-405.2171; Use: The 
requirements associated with the Medicare and Medicaid Conditions for 
Coverage for Suppliers of ESRD Services fall into two categories: 
record keeping requirements and reporting requirements. With regard to 
the recordkeeping requirements, CMS uses these conditions for coverage 
to certify health care facilities that want to participate in the 
Medicare or Medicaid

[[Page 17888]]

programs. These record keeping requirements are no different than other 
conditions for coverage in that they reflect comparable standards 
developed by industry organizations such as the Renal Physicians 
Association, American Society of Transplant Surgeons, and the National 
Association of Patients on Hemodialysis and Transplantation. With 
respect to reporting requirements, the information is needed to assess 
and ensure proper distribution and effective utilization of ESRD 
treatment resources while maintaining or improving quality of care. It 
is CMS's responsibility to closely monitor ESRD service utilization to 
prevent over-expansion of facilities and resultant under-utilization.; 
Form Number: CMS-R-52 (OMB: 0938-0386); Frequency: 
Recordkeeping and Reporting--Annually; Affected Public: Business or 
other for-profit and Federal government; Number of Respondents: 4,757; 
Total Annual Responses: 4,757; Total Annual Hours: 160,702.
    2. Type of Information Collection Request: Extension of a currently 
approved collection; Title of Information Collection: Medicare 
Disproportionate Share Adjustment Procedures and Criteria and 
Supporting Regulations in 42 CFR 412.106; Use: A hospital's 
disproportionate share adjustment is determined by its fiscal 
intermediary (FI) using a combination of Medicare Part A and 
Supplemental Security Income data provided by CMS, and Medicaid data 
calculated from the hospital's cost report. The data provided through 
these calculations are then compared to the qualifying criteria located 
in 42 CFR 412.106 to determine the final adjustment. If these 
calculations, based on the Federal fiscal year, do not allow the 
hospital to qualify for a disproportionate share adjustment, the 
hospital may request that the calculations be performed using its cost 
reporting period.; Form Number: CMS-R-194 (OMB: 0938-0691); 
Frequency: Recordkeeping and Reporting--On occasion; Affected Public: 
Business or other for-profit and Not-for-profit institutions; Number of 
Respondents: 100; Total Annual Responses: 100; Total Annual Hours: 100.
    To obtain copies of the supporting statement and any related forms 
for the proposed paperwork collections referenced above, access CMS' 
Web site address at https://www.cms.hhs.gov/PaperworkReductionActof1995, 
or E-mail your request, including your address, phone number, OMB 
number, and CMS document identifier, to Paperwork@cms.hhs.gov, or call 
the Reports Clearance Office on (410) 786-1326.
    To be assured consideration, comments and recommendations for the 
proposed information collections must be received at the address below, 
no later than 5 p.m. on June 6, 2006. CMS, Office of Strategic 
Operations and Regulatory Affairs, Division of Regulations 
Development--B, Attention: William N. Parham, III, Room C4-26-05, 7500 
Security Boulevard, Baltimore, Maryland 21244-1850.

    Dated: March 30, 2006.
Michelle Shortt,
Director, Regulations Development Group, Office of Strategic Operations 
and Regulatory Affairs.
 [FR Doc. E6-4947 Filed 4-6-06; 8:45 am]
BILLING CODE 4120-01-P

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