Agency Forms Undergoing Paperwork Reduction Act Review, 9558-9559 [06-1779]
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9558
Federal Register / Vol. 71, No. 37 / Friday, February 24, 2006 / Notices
collection. All comments will become a
matter of public record.
Dated: February 16, 2006.
Carolyn M. Clancy,
Director.
[FR Doc. 06–1716 Filed 2–23–06; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Agency for Healthcare Research and
Quality
Meetings on Patient Safety and Quality
Improvement
Agency for Healthcare Research
and Quality (AHRQ), HHS.
ACTION: Notice of public meetings,
including telephone call-in.
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AGENCY:
SUMMARY: We are considering how to
implement the Patient Safety and
Quality Improvement Act of 2005 (Act),
including such questions as how the Act
might be applied to various
organizational configurations and how
best to ensure that the statute’s
fundamental confidentiality objectives
are achieved. To help us better
understand the thinking and plans of
providers that are interested in seeking
out patient safety organization (PSO)
services, and of entities that anticipate
establishing such an organization, this
notice invites the public to provide
information that may assist the Agency,
either in person or by telephone call-in,
at three related public meetings.
DATES: The three public meetings will
be held on Wednesday, March 8, 2006;
Monday, March 13, 2006; and Thursday,
March 16, 2006. Each meeting will be
held from 12:30 p.m. EST until finished
(no later than 3:30 p.m. EST).
ADDRESSES: The meetings on March 8
and 13 will be held at AHRQ, John M.
Eisenberg Building, 540 Gaither Road,
Rockville, MD 20850. The meeting on
March 16 will be held at Hilton
Washington Embassy Row, 2015
Massachusetts Ave. NW., Washington,
DC 20036.
FOR FURTHER INFORMATION CONTACT:
Eileen Hogan, Agency for Healthcare
Research and Quality, 540 Gaither Road,
Rockville, MD 20850; Telephone: 301–
427–1307; E-mail:
Eileen.Hogan@ahrq.hhs.gov.
SUPPLEMENTARY INFORMATION: The Act is
intended to help health care providers
improve patient safety, reduce the
incidence of events that adversely effect
patient safety, and otherwise improve
the quality of health care delivery. More
specifically, the Act, by establishing a
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Federal privilege and mandating
confidentiality protection, encourages
health care providers to contract with
PSOs to collect and analyze data on
patient safety events (including ‘‘near
misses,’’ ‘‘close calls,’’ and ‘‘no-harm’’
events as well as other types of patient
safety events), to develop and
disseminate information to improve
patient safety, and to provide feedback
and assistance to reduce patient risk.
The decision to contract with a PSO is
voluntary.
Registration and Other Information
About the Meetings
We request that interested persons
register with the Cygnus Corporation on
the Internet at https://www.cygnusc.com/
to participate in one or more meetings
either in person or by telephone. The
contact at Cygnus Corporation is Megan
Griggs who can be reached by telephone
at (301) 231–7537, ext. 260 and by email at griggsm@cygnus.com. Interested
persons should register at least the day
before a meeting in which they wish to
participate. Non-registered individuals
will be able to attend a meeting in
person if space is available. However,
we will not be able to provide a
telephone hook-up for those that do not
register at least the day before the
meeting.
If sign language interpretation or other
reasonable accommodation for a
disability is needed, please contact Mr.
Donald L. Inniss, Director, Office of
Equal Employment Opportunity
Program Support Center, on (301) 443–
1144.
Each public meeting is scheduled for
a three-hour period, but will end sooner
if participants have finished providing
input before the time period expires. We
are asking for input concerning specific
topics as follows:
March 8, 2006: Provider—PSO
relationships, contracts, and
disclosures. March 13, 2006: Operation
of a component PSO (a PSO that is part
of another organization). March 16,
2006: Security and Confidentiality
issues.
We request that input regarding the
specified topics be provided at the
meeting scheduled for that topic. After
those who wish to provide input on the
specific topics have finished,
participants will be welcome to provide
input on other issues regarding the
implementation of the Act. The format
for the meetings is intended to allow
participants not only to provide input,
but also to respond to the input
provided by others. We especially
request input from entities interested in
becoming or creating PSOs and from
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providers interested in contracting with
PSOs.
To help interested individuals
prepare for the meetings, we invite
review of the Act. The full text is set
forth on the Internet at: https://
www.gpoaccess.gov/plaws/ (search for
‘‘Public Law 109—41.’’)
Also, we will establish an e-mail
notification list to provide interested
parties with automatic notification of
relevant information posted on the
AHRQ Web site (https://www.ahrq.gov)
concerning the PSO program. To be
added to the e-mail notification list,
send your e-mail address to
Eileen.Hogan@ahrq.hhs.gov and use the
words ‘‘Add me to the list’’ in the
subject line.
These meetings will be primarily
listening sessions for the Agency and
potentially an opportunity for dialogue
among participants. We believe that the
input received at the public meetings
will be most helpful in providing the
Agency with background information,
fostering fact finding, and broadening
awareness of issues raised by the
legislation. We generally will not
respond to the presentations during the
meetings and will not regard them as
formal comments that must be
addressed in later rulemaking
documents.
Dated: February 17, 2006.
Carolyn M. Clancy,
Director.
[FR Doc. 06–1725 Filed 2–23–06; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–06–0576]
Agency Forms Undergoing Paperwork
Reduction Act Review
The Centers for Disease Control and
Prevention (CDC) publishes a list of
information collection requests under
review by the Office of Management and
Budget (OMB) in compliance with the
Paperwork Reduction Act (44 U.S.C.
Chapter 35). To request a copy of these
requests, call the CDC Reports Clearance
Officer at (404) 639–5960 or send an email to omb@cdc.gov. Send written
comments to CDC Desk Officer, Office of
Management and Budget, Washington,
DC or by fax to (202) 395–6974.
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Federal Register / Vol. 71, No. 37 / Friday, February 24, 2006 / Notices
Notice of Correction
Title of Project
Possession, Use, and Transfer of
Select Agents and Toxins (OMB Control
No. 0920–0576)—Extension—Office of
the Director (OD), Centers for Disease
Control and Prevention (CDC).
Description of Correction
Due to a clerical oversight, the closing
date of the 30-day Federal Register
Notice (FRN) under 30dy–06–0576
published on January 24, 2006 will be
used as the official 30-day for the OMB
submission printed under that notice
number. The closing date of the 30-day
FRN under 30dy–06–0576 dated
February 8, 2006 will not be used. The
second 30-day FRN was inadvertently
published, so please disregard the
second closing date.
Comments will be considered until
COB of February 24, 2006 and not
March 8, 2006.
Dated: February 21, 2006.
Joan F. Karr,
Acting Reports Clearance Officer, Centers for
Disease Control and Prevention.
[FR Doc. 06–1779 Filed 2–23–06; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier: CMS–1450(UB–04)]
Agency Information Collection
Activities: Proposed Collection;
Comment Request
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.
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AGENCY:
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1. Type of Information Collection
Request: New Collection; Title of
Information Collection: Medicare
Uniform Institutional Provider Bill and
Supporting Regulations in 42 CFR
424.5; Use: Section 42 CFR 424.5(a)(5)
requires providers of services to submit
a claim for payment prior to any
Medicare reimbursement. Charges billed
are coded by revenue codes. The bill
specifies diagnoses according to the
International Classification of Diseases,
Ninth Edition (ICD–9-CM) code.
Inpatient procedures are identified by
ICD–9–CM codes, and outpatient
procedures are described using the CMS
Common Procedure Coding System
(HCPCS). These are standard systems of
identification for all major health
insurance claims payers. Submission of
information on the CMS–1450 permits
Medicare intermediaries to receive
consistent data for proper payment. All
hardcopy claims processed by Medicare
fiscal intermediaries must be submitted
on the CMS–1450 (UB–04) after May 23,
2007. Data fields in the X12N 837 data
set are consistent with the CMS–1450
(UB–04) data set.; Form Numbers: CMS–
1450 (UB–04) (OMB#: 0938–NEW);
Frequency: Reporting—On occasion;
Affected Public: Not-for-profit
institutions, Business or other for-profit;
Number of Respondents: 53,111; Total
Annual Responses: 179,489,721; Total
Annual Hours: 308,237.
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.
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 April 25, 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: February 16, 2006.
Michelle Shortt,
Director, Regulations Development Group,
Office of Strategic Operations and Regulatory
Affairs.
[FR Doc. 06–1767 Filed 2–23–06; 8:45 am]
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9559
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare and Medicaid
Services
[Document Identifier: CMS–10182]
Emergency Clearance: Public
Information Collection Requirements
Submitted to the Office of Management
and Budget (OMB)
Center for Medicare and
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 and Medicaid
Services (CMS), Department of Health
and Human Services, 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.
We are, however, requesting an
emergency review of the information
collection referenced below. In
compliance with the requirement of
section 3506(c)(2)(A) of the Paperwork
Reduction Act of 1995, we have
submitted to the Office of Management
and Budget (OMB) the following
requirements for emergency review. We
are requesting an emergency review
because the collection of this
information is needed before the
expiration of the normal time limits
under OMB’s regulations at 5 CFR part
1320. This is necessary to ensure
compliance with an initiative of the
Administration. CMS does not have
sufficient time to complete the normal
PRA clearance process. Section 1860D–
1 of the Medicare Prescription Drug,
Improvement, and Modernization Act of
2003 (MMA) and implementing
regulations at 42 CFR 423.56(c) and (d)
requires that all entities provide a
disclosure of creditable coverage status
to all Medicare Part D eligible
individuals. The normal PRA clearance
process would result in violating this
statute which would result in public
harm to enrolled Medicare prescription
drug beneficiaries.
AGENCY:
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Agencies
[Federal Register Volume 71, Number 37 (Friday, February 24, 2006)]
[Notices]
[Pages 9558-9559]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 06-1779]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30Day-06-0576]
Agency Forms Undergoing Paperwork Reduction Act Review
The Centers for Disease Control and Prevention (CDC) publishes a
list of information collection requests under review by the Office of
Management and Budget (OMB) in compliance with the Paperwork Reduction
Act (44 U.S.C. Chapter 35). To request a copy of these requests, call
the CDC Reports Clearance Officer at (404) 639-5960 or send an e-mail
to omb@cdc.gov. Send written comments to CDC Desk Officer, Office of
Management and Budget, Washington, DC or by fax to (202) 395-6974.
[[Page 9559]]
Notice of Correction
Title of Project
Possession, Use, and Transfer of Select Agents and Toxins (OMB
Control No. 0920-0576)--Extension--Office of the Director (OD), Centers
for Disease Control and Prevention (CDC).
Description of Correction
Due to a clerical oversight, the closing date of the 30-day Federal
Register Notice (FRN) under 30dy-06-0576 published on January 24, 2006
will be used as the official 30-day for the OMB submission printed
under that notice number. The closing date of the 30-day FRN under
30dy-06-0576 dated February 8, 2006 will not be used. The second 30-day
FRN was inadvertently published, so please disregard the second closing
date.
Comments will be considered until COB of February 24, 2006 and not
March 8, 2006.
Dated: February 21, 2006.
Joan F. Karr,
Acting Reports Clearance Officer, Centers for Disease Control and
Prevention.
[FR Doc. 06-1779 Filed 2-23-06; 8:45 am]
BILLING CODE 4163-18-P