66956 Federal Register / Vol. 71, No.
222 / Friday, November 17, 2006 / Notices
addition, CMS has established policies
to limit payment abuse that will be
based on FIs tracking patient movement
among these co-located providers. Form
Number: CMS–10088 (OMB#: 0938–
0897; Frequency: Reporting—as needed;
Affected Public: Business or other for
profit and Not-for-profit institutions;
Number of Respondents: 200; Total
Annual Responses: 200; Total Annual
Hours: 50.
2. Type of Information Collection
Request: Revision of a currently
approved collection; Title of
Information Collection: Conditions of
Coverage for Organ Procurement
Organizations (OPOs) and Supporting
Regulations in 42 CFR 486.301–348;
Use: Organ Procurement Organizations
are required to submit accurate data to
CMS through the Organ Procurement
and Transplantation Network (OPTN).
The data concerns the organ
procurement activities, as well as
various OPO business activities,
including information on its designated
service area; structure; various policies,
procedures, and protocols; and its
quality assessment and performance
improvement (QAPI) program. This
information is necessary to assure
maximum effectiveness in the
procurement and distribution of organs.
Form Number: CMS–R–13 (OMB#:
0938–0688; Frequency: Reporting—
Every 4 years and as needed; Affected
Public: Not-for-profit institutions;
Number of Respondents: 58; Total
Annual Responses: 58; Total Annual
Hours: 21,427.
To obtain copies of the supporting
statement and any related forms for the
proposed paperwork collections
referenced above, access CMS Web site
address at http://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.
Written comments and
recommendations for the proposed
information collections must be mailed
or faxed within 30 days of this notice
directly to the OMB desk officer: OMB
Human Resources and Housing Branch,
Attention: Carolyn Lovett, New
Executive Office Building, Room 10235,
jlentini on PROD1PC65 with NOTICES
Washington, DC 20503, Fax Number:
(202) 395–6974.
VerDate Aug<31>2005 16:31 Nov 16, 2006 Jkt 211001
Dated: November 7, 2006.
Michelle Shortt,
Director, Regulations Development Group,
Office of Strategic Operations and Regulatory
Affairs.
[FR Doc. E6–19430 Filed 11–16–06; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier: CMS-R–235]
Agency Information Collection
Activities: Proposed Collection;
Comment Request
AGENCY: Centers for Medicare &
Medicaid Services, HHS.
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: Data Use
Agreement Information Collection
Requirements, Model Language and
Supporting Regulations in 45 CFR part
5b. Use: The Data Use Agreement (DUA)
is needed as part of the review of each
CMS data request to ensure compliance
with the requirements of the Privacy Act
for disclosure of data that contain
individually-identifiable information. In
addition, the DUA is used to maintain
appropriate accounting and tracking of
disclosures of records from Privacy Act
systems of records. Form Number: CMS-
R–235 (OMB#: 0938–0734); Frequency:
Reporting-On occasion; Affected Public:
Not-for-profit institutions; Number of
Respondents: 1,500; Total Annual
Responses: 1,500; Total Annual Hours:
750.
PO 00000 Frm 00050 Fmt 4703 Sfmt 4703 E:\FR\FM\17NON1.SGM
To obtain copies of the supporting
statement and any related forms for the
proposed paperwork collections
referenced above, access CMS’ Web Site
address at http://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 January 16, 2007.
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: November 7, 2006.
Michelle Shortt,
Director, Regulations Development Group,
Office of Strategic Operations and Regulatory
Affairs.
[FR Doc. E6–19431 Filed 11–16–06; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
Clinical Chemistry and Clinical
Toxicology Devices Panel of the
Medical Devices Advisory Committee;
Notice of Meeting
AGENCY: Food and Drug Administration,
HHS.
ACTION: Notice.
This notice announces a forthcoming
meeting of a public advisory committee
of the Food and Drug Administration
(FDA). The meeting will be open to the
public.
Name of Committee: Clinical
Chemistry and Clinical Toxicology
Devices Panel of the Medical Devices
Advisory Committee.
General Function of the Committee:
To provide advice and
recommendations to the agency on
FDA’s regulatory issues.
Date and Time: The meeting will be
held on December 6, 2006, from 8 a.m.
to 4:30 p.m.
Location: Holiday Inn, Ballroom, Two
Montgomery Village Ave., Gaithersburg,
MD.
Contact Person: Veronica J. Calvin,
Center for Devices and Radiological
Health (HFZ–440), Food and Drug
Administration, 2098 Gaither Rd.,
17NON1