Agency Information Collection Activities: Proposed Collection; Comment Request, 21349-21351 [E8-8440]
Download as PDF
Federal Register / Vol. 73, No. 77 / Monday, April 21, 2008 / Notices
indicated. The applications also will be
available for inspection at the offices of
the Board of Governors. Interested
persons may express their views in
writing on the standards enumerated in
the BHC Act (12 U.S.C. 1842(c)). If the
proposal also involves the acquisition of
a nonbanking company, the review also
includes whether the acquisition of the
nonbanking company complies with the
standards in section 4 of the BHC Act
(12 U.S.C. 1843). Unless otherwise
noted, nonbanking activities will be
conducted throughout the United States.
Additional information on all bank
holding companies may be obtained
from the National Information Center
Web site at www.ffiec.gov/nic/.
Unless otherwise noted, comments
regarding each of these applications
must be received at the Reserve Bank
indicated or the offices of the Board of
Governors not later than May 16, 2008.
A. Federal Reserve Bank of Atlanta
(David Smith, Vice President) 1000
Peachtree Street, N.E., Atlanta, Georgia
30309:
1. Commerce Union Bancshares, Inc.;
to become a bank holding company by
acquiring 100 percent of the voting
shares of Commerce Union Bank, both
of Springfield, Tennessee.
B. Federal Reserve Bank of Dallas
(W. Arthur Tribble, Vice President) 2200
North Pearl Street, Dallas, Texas 75201–
2272:
1. Algodon de Calidad Bancshares,
Inc.; to become a bank holding company
by acquiring 100 percent of the voting
shares of The First State Bank, both of
Abernathy, Texas.
Board of Governors of the Federal Reserve
System, April 16, 2008.
Robert deV. Frierson,
Deputy Secretary of the Board.
[FR Doc.E8–8551 Filed 4–18–08; 8:45 am]
BILLING CODE 6210–01–S
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Agency for Healthcare Research and
Quality
Agency Information Collection
Activities: Proposed Collection;
Comment Request
Agency for Healthcare Research
and Quality, Department of Health and
Human Services.
ACTION: Notice.
rwilkins on PROD1PC63 with NOTICES
AGENCY:
This notice announces the
intention of the Agency for Healthcare
Research and Quality (AHRQ) to request
that the Office of Management and
Budget (OMB) allow information
SUMMARY:
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16:59 Apr 18, 2008
Jkt 214001
collection related to implementation of
the Patient Safety and Quality
Improvement Act of 2005, 42 U.S.C.
299b–21 to 299b–26, in: ‘‘Patient Safety
Organization Certification and Related
Forms and a Patient Safety
Confidentiality Complaint Form.’’ In
accordance with the Paperwork
Reduction Act of 1995, 44 U.S.C.
3506(c)(2)(A), AHRQ invites the public
to comment on this proposed
information collection.
This proposed information collection
was previously published in the Federal
Register on February 20th, 2008 and
allowed 60 days for public comment.
The purpose of this notice is to allow an
additional 30 days for public comment.
DATES: Comments on this notice must be
received by May 21, 2008.
ADDRESSES: Written comments should
be submitted to: AHRQ’s OMB Desk
Officer by fax at (202) 395–6974
(attention: AHRQ’s desk officer) or by email at OIRA_submission@omb.eop.gov
(attention: AHRQ’s desk officer).
Copies of the proposed collection
plans, data collection instruments, and
specific details on the estimated burden
can be obtained from AHRQs Reports
Clearance Officer.
FOR FURTHER INFORMATION CONTACT:
Doris Lefkowitz, AHRQ, Reports
Clearance Officer, (301) 427–1477.
SUPPLEMENTARY INFORMATION: ‘‘Patient
Safety Organization Certification and
Related Forms and a Patient Safety
Confidentiality Complaint Form.’’
The Department of Health and Human
Services (HHS) Agency for Healthcare
Research and Quality (AHRQ) has been
delegated the authority to implement
the provisions of the Patient Safety and
Quality Improvement Act of 2005 (for
brevity referenced here as the Patient
Safety Act) that call for submission to
the Secretary of certifications by entities
seeking to become listed by the
Secretary as Patient Safety
Organizations (PSOs). These entities
must certify that they meet or will meet
specified statutory criteria and
requirements for PSOs.
The HHS Office for Civil Rights (OCR)
has been delegated the authority to
enforce the provisions of the Patient
Safety Act that mandate confidentiality
of ‘‘patient safety work product.’’ This
term is defined in the statute, at 42
U.S.C. 299b–21(7), and further
explained in the related Notice of
Proposed Rulemaking published in the
Federal Register on February 12, 2008,
73 FR 8112–8183. Individuals may
voluntarily submit complaints to OCR if
they believe that an individual or
organization in possession of patient
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21349
safety work product unlawfully
disclosed it.
Methods of Collection
While there are a number of
information collection forms described
below, they will be implemented at
different times, some near the end of the
three year approval period for these
standard forms. The forms for
certifications of information will collect
only the minimum amount of
information from entities necessary for
the Secretary to determine compliance
with statutory requirements for PSOs,
i.e., each of the required certification
forms will consist of short attestations
followed by ‘‘yes’’ and ‘‘no’’ checkboxes
to be checked and initialed.
Initial PSO Certification and PSO
Recertification Forms
The Patient Safety Act, in 42 U.S.C.
299b–24(a) and the proposed rule in 45
CFR 3.102 provide that an entity may
seek an initial three-year listing as a
PSO by submitting an initial
certification that it has policies and
procedures in place to perform eight
patient safety activities (enumerated in
the statute and the proposed regulation),
and that it will comply, upon listing,
with seven other statutory criteria. The
draft initial certification form also
includes four questions related to other
requirements for listing related to
eligibility and pertinent organizational
history. Similarly, the proposed
certification form for continued listing
as a PSO (for each successive three-year
period after the initial listing period)
would require certifications that the
PSO is performing, and will continue to
perform, the eight patient safety
activities, and is complying with, and
will continue to comply with, the seven
statutory criteria. The average annual
burden in the first three years of 17
hours per year for the collection of
information requested by the
certification forms for initial and
continued listing is based upon a total
average estimate of 33 respondents per
year and an estimated time of 30
minutes per response. Information
collection, i.e., collection of initial
certification forms, will begin as soon as
the forms are approved for use.
Collection of forms for continued listing
will not begin until several months
before a date that is three years after the
first PSOs are listed by the Secretary.
(See Note after Exhibit 1.)
Two-Contract Certification
To implement 42 U.S.C. 299b–
24(b)(1)(C), AHRQ plans to adopt the
following procedure, published in the
proposed regulation: In order to
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Federal Register / Vol. 73, No. 77 / Monday, April 21, 2008 / Notices
maintain its PSO listing, a PSO will be
required only to submit a brief
attestation, at least once in every 24month period after its initial date of
listing, indicating that it has entered
into contracts with two providers. The
annualized burden of 8 hours for the
collection of information requested by
the two-contract requirement is based
upon an estimate of 33 respondents per
year and an estimated 15 minutes per
response. This collection of information
will begin when the first PSO timely
notifies the Secretary that it has entered
into two contracts.
Disclosure Form
The Patient Safety statute at 42 U.S.C.
299b-24(b)(1)(E) requires a PSO to fully
disclose information to the Secretary if
the PSO has additional financial,
contractual, or reporting relationships
with any provider to which the PSO
provides services pursuant to the
Patient Safety Act under contract or if
the PSO is managed or controlled by, or
is not operated independently from, any
of its contracting providers. Disclosure
forms will be collected only when a
PSO has such relationships with a
contracting provider to report. The
Secretary is required to review each
disclosure statement and make public
findings as to whether a PSO can fairly
and accurately carry out its
responsibilities. AHRQ assumes that
only a small percentage of entities will
need to file such disclosure forms.
However, AHRQ is providing a high
estimate of 17 respondents annually and
thus presumably overestimating
respondent burden. In summary, the
annual burden of 8 hours for the
collection of information requested by
the disclosure form is based upon the
high estimate of 17 respondents per year
and an estimated 30 minutes per
response. This information collection
will begin when a PS0 first reports
having any of the specified types of
additional relationships with a health
care provider with which it has a
contract to carry out patient safety
activities.
PSO Information Form
Annual completion of a PSO
information form will be voluntary and
will provide information to HHS on the
type of healthcare settings that PSOs are
working with to carry out patient safety
activities. This form is designed to
collect a minimum amount of data in
order to gather aggregate statistics on the
reach of the Patient Safety Act with
respect to types of institutions
participating and their general location
in the United States. This information
will be included in AHRQ’s annual
quality report, as required under section
923(c) of the Patient Safety Act. No
PSO-specific data will be released
without PSO consent. The overall
annual burden estimate of 17 hours for
the collection of information requested
by the PSO Information Form is based
upon an estimate of 33 respondents per
year and an estimated 30 minutes per
response. This information collection
will begin toward the end of the
calendar year in which the first PSOs
are listed by the Secretary.
OCR Complaint Form
The complaint form will collect from
individuals only the minimum amount
of information necessary for OCR to
process and assess incoming
complaints. The overall annual burden
estimate of 17 hours for the collection
of information requested by the
underlying form is based upon an
estimate of 50 respondents per year and
an estimated 20 minutes per response.
OCR’s information collection using this
form will not begin until after there is
at least one PSO receiving and
generating patient safety work product
and there is an allegation of a violation
of the statutory protection of patient
safety work product.
All Administrative Forms
The overall maximum anticipated
annual burden estimate is 75 hours for
all the above described collections of
information. Because the forms filled
out by PSOs vary over each of their first
three years, the table below includes
three-year total estimates divided by
three to arrive at an annual estimate of
burden hours. (See below.)
EXHIBIT 1.—ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Form
Number of
responses per
respondent
Hours per
response
Total burden
hours
100/3
50/3
50/3
100/3
100/3
150/3
1
1
1
1
1
1
30/60
30/60
30/60
15/60
30/60
20/60
17
8
8
8
17
17
Total**** ....................................................................................................
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Patient Safety Organization Certification Form ...............................................
Recertification Form* .......................................................................................
Disclosure Form ...............................................................................................
Two-Contract Requirement Form** .................................................................
Information Form*** .........................................................................................
Patient Safety Confidentiality Complaint Form ................................................
500/3
na
na
75
Note: * The Recertification Form will be completed by any interested PSO at least 45 days before the end of its current three-year listing period. The three-year period for computing respondent burden begins with the date when the approved forms are officially made available for submission. Thus the burden period does not correspond exactly to the three-year period of listing. The burden period begins shortly (approximately
30 days) before any PSO’s listing period. As a result, the burden for the first PSOs to submit certifications for continued listing at least 45 days
before their listing lapses is likely to fall just before the three-year anniversary of their first burden, i.e. their completion of their initial certifications
and before the end of their third year of listing. We assume completing this form will require 30 minutes, the same time as for the Certification
Form. In the out-years, we expect the number of PSOs to remain stable, with the number of new entrants offset by the number of entities that
will relinquish their status or be revoked.
** The Two-Contract Requirement Form will be completed by each PSO within the 24-month period after initial listing by the Secretary.
*** The Information Form will collect data by calendar year, beginning close to the end of the calendar year when PSOs are first listed.
**** A total of 100 PSOs are expected to apply over three years: 50 in year 1; 25 in year 2; and 25 in year 3. Relationship Disclosure, TwoContract, and even voluntary Information Forms may be submitted by individual PSOs in different years. OCR is anticipating considerable variation in the number of complaints per year. Hence we have expressed the total for each year as the average of the expected total over the three
year collection period.
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Federal Register / Vol. 73, No. 77 / Monday, April 21, 2008 / Notices
EXHIBIT 2.—ESTIMATED ANNUALIZED COST BURDEN
Number of
respondents
Form
Total burden
hours
Average
hourly wage
rate
Total cost
burden
Patient Safety Organization Certification Form ...............................................
Recertification Form .........................................................................................
Disclosure Form ...............................................................................................
Two-Contract Requirement Form ....................................................................
Information Form .............................................................................................
Patient Safety Confidentiality Complaint Form ................................................
100/3
50/3
50/3
100/3
100/3
150/3
17
8
8
8
17
17
$29.82
29.82
29.82
29.82
29.82
29.82
$506.94
238.56
238.56
506.94
506.94
506.94
Total ..........................................................................................................
500/3
67
29.82
2,504.88
Estimated Annual Costs to the Federal
Government
Description
a. AHRQ
By statute, AHRQ must collect and
review certifications from an entity that
seeks listing or continued listing as a
PSO under the Patient Safety Act.
Additional information collection is
also required for entities to remain
listed as a PSO (i.e., submissions
regarding compliance with the twocontract requirement and reports of
certain relationships between a PSO and
each of its contracting providers). The
cost to AHRQ of processing the
information collected with the abovedescribed forms is minimal; an
estimated equivalent of only
approximately 0.05 FTE or $7,500 per
year for each agency and virtually no
new overhead costs.
Description
Amount
Personnel & Support Staff ............
Consultant (sub-contractor) services ............................................
Equipment .....................................
Supplies ........................................
All other expenses ........................
Average Annual Cost ...................
$7,500
0
0
0
0
7,500
rwilkins on PROD1PC63 with NOTICES
b. OCR
OCR cannot conduct its work without
collecting information through its
proposed complaint forms. Even if OCR
did not use complaint forms and only
took information orally, it would still
have to capture the same information in
order to begin processing a complaint.
Therefore, the incremental cost to OCR
of processing the information collected
from the complaint form is minimal and
is equivalent to only approximately 0.05
FTE or $7,500 per year with, with
virtually no new overhead costs.
Description
16:59 Apr 18, 2008
All other expenses ........................
Average Annual Cost ...................
In accordance with the above-cited
Paperwork Reduction Act legislation,
comments on the above-described
AHRQ and OCR information collection
to implement the Patient Safety Act are
requested with regard to any of the
following: (a) Whether the proposed
collection of information is necessary
for the proper performance of AHRQ
health care research, quality
improvement and information
dissemination functions, including
whether the information will have
practical utility; (b) the accuracy of
AHRQ’s estimate of burden (including
hours and costs) of the proposed
collection(s) of information; (c) ways to
enhance the quality, utility, and clarity
of the information to be collected; and
(d) ways to minimize the burden of the
collection of information upon the
respondents, including the use of
automated collection techniques or
other forms of information technology.
Comments submitted in response to
this notice will be summarized and
included in the Agency’s subsequent
request for OMB approval of the
proposed information collection.
All comments will become a matter of
public record.
Dated: April 14, 2008.
Carolyn M. Clancy,
Director, AHRQ.
[FR Doc. E8–8440 Filed 4–18–08; 8:45 am]
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$7,500
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0
7,500
Request for Comments
Amount
Personnel & Support Staff ............
Consultant (sub-contractor) services ............................................
Equipment .....................................
Supplies ........................................
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Amount
0
0
0
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Agency for Healthcare Research and
Quality
Agency Information Collection
Activities: Proposed Collection;
Comment Request
Agency for Healthcare Research
and Quality, HHS.
AGENCY:
ACTION:
Notice.
SUMMARY: This notice announces the
intention of the Agency for Healthcare
Research and Quality (AHRQ) to request
that the Office of Management and
Budget (OMB) approve the proposed
information collection project:
Technical Assistance for Health IT and
Health Information Exchange in
Medicaid and SCHIP. In accordance
with the Paperwork Reduction Act of
1995, 44 U.S.C. 3506(c)(2)(A), AHRQ
invites the public to comment on this
proposed information collection.
This proposed information collection
was previously published in the Federal
Register on February 20th, 2008 and
allowed 60 days for public comment. No
comments were received. The purpose
of this notice is to allow an additional
30 days for public comment.
Comments on this notice must be
received by May 21, 2008.
ADDRESSES: Written comments should
be submitted to: AHRQ’s OMB Desk
Officer by fax at (202) 395–6974
(attention: AHRQ’s desk officer) or by email at OIRA_submission@omb.eop.gov
(attention: AHRQ’s desk officer).
Copies of the proposed collection
plans, data collection instruments, and
specific details on the estimated burden
can be obtained from the AHRQ Reports
Clearance Officer.
FOR FURTHER INFORMATION CONTACT:
Doris Lefkowitz, AHRQ Reports
Clearance Officer, (301) 427–1477, or by
e-mail at doris.letkowitz@ahrg.hhs.gov.
SUPPLEMENTARY INFORMATION:
DATES:
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Agencies
[Federal Register Volume 73, Number 77 (Monday, April 21, 2008)]
[Notices]
[Pages 21349-21351]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E8-8440]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Agency for Healthcare Research and Quality
Agency Information Collection Activities: Proposed Collection;
Comment Request
AGENCY: Agency for Healthcare Research and Quality, Department of
Health and Human Services.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: This notice announces the intention of the Agency for
Healthcare Research and Quality (AHRQ) to request that the Office of
Management and Budget (OMB) allow information collection related to
implementation of the Patient Safety and Quality Improvement Act of
2005, 42 U.S.C. 299b-21 to 299b-26, in: ``Patient Safety Organization
Certification and Related Forms and a Patient Safety Confidentiality
Complaint Form.'' In accordance with the Paperwork Reduction Act of
1995, 44 U.S.C. 3506(c)(2)(A), AHRQ invites the public to comment on
this proposed information collection.
This proposed information collection was previously published in
the Federal Register on February 20th, 2008 and allowed 60 days for
public comment. The purpose of this notice is to allow an additional 30
days for public comment.
DATES: Comments on this notice must be received by May 21, 2008.
ADDRESSES: Written comments should be submitted to: AHRQ's OMB Desk
Officer by fax at (202) 395-6974 (attention: AHRQ's desk officer) or by
e-mail at OIRA_submission@omb.eop.gov (attention: AHRQ's desk
officer).
Copies of the proposed collection plans, data collection
instruments, and specific details on the estimated burden can be
obtained from AHRQs Reports Clearance Officer.
FOR FURTHER INFORMATION CONTACT: Doris Lefkowitz, AHRQ, Reports
Clearance Officer, (301) 427-1477.
SUPPLEMENTARY INFORMATION: ``Patient Safety Organization Certification
and Related Forms and a Patient Safety Confidentiality Complaint
Form.''
The Department of Health and Human Services (HHS) Agency for
Healthcare Research and Quality (AHRQ) has been delegated the authority
to implement the provisions of the Patient Safety and Quality
Improvement Act of 2005 (for brevity referenced here as the Patient
Safety Act) that call for submission to the Secretary of certifications
by entities seeking to become listed by the Secretary as Patient Safety
Organizations (PSOs). These entities must certify that they meet or
will meet specified statutory criteria and requirements for PSOs.
The HHS Office for Civil Rights (OCR) has been delegated the
authority to enforce the provisions of the Patient Safety Act that
mandate confidentiality of ``patient safety work product.'' This term
is defined in the statute, at 42 U.S.C. 299b-21(7), and further
explained in the related Notice of Proposed Rulemaking published in the
Federal Register on February 12, 2008, 73 FR 8112-8183. Individuals may
voluntarily submit complaints to OCR if they believe that an individual
or organization in possession of patient safety work product unlawfully
disclosed it.
Methods of Collection
While there are a number of information collection forms described
below, they will be implemented at different times, some near the end
of the three year approval period for these standard forms. The forms
for certifications of information will collect only the minimum amount
of information from entities necessary for the Secretary to determine
compliance with statutory requirements for PSOs, i.e., each of the
required certification forms will consist of short attestations
followed by ``yes'' and ``no'' checkboxes to be checked and initialed.
Initial PSO Certification and PSO Recertification Forms
The Patient Safety Act, in 42 U.S.C. 299b-24(a) and the proposed
rule in 45 CFR 3.102 provide that an entity may seek an initial three-
year listing as a PSO by submitting an initial certification that it
has policies and procedures in place to perform eight patient safety
activities (enumerated in the statute and the proposed regulation), and
that it will comply, upon listing, with seven other statutory criteria.
The draft initial certification form also includes four questions
related to other requirements for listing related to eligibility and
pertinent organizational history. Similarly, the proposed certification
form for continued listing as a PSO (for each successive three-year
period after the initial listing period) would require certifications
that the PSO is performing, and will continue to perform, the eight
patient safety activities, and is complying with, and will continue to
comply with, the seven statutory criteria. The average annual burden in
the first three years of 17 hours per year for the collection of
information requested by the certification forms for initial and
continued listing is based upon a total average estimate of 33
respondents per year and an estimated time of 30 minutes per response.
Information collection, i.e., collection of initial certification
forms, will begin as soon as the forms are approved for use. Collection
of forms for continued listing will not begin until several months
before a date that is three years after the first PSOs are listed by
the Secretary. (See Note after Exhibit 1.)
Two-Contract Certification
To implement 42 U.S.C. 299b-24(b)(1)(C), AHRQ plans to adopt the
following procedure, published in the proposed regulation: In order to
[[Page 21350]]
maintain its PSO listing, a PSO will be required only to submit a brief
attestation, at least once in every 24-month period after its initial
date of listing, indicating that it has entered into contracts with two
providers. The annualized burden of 8 hours for the collection of
information requested by the two-contract requirement is based upon an
estimate of 33 respondents per year and an estimated 15 minutes per
response. This collection of information will begin when the first PSO
timely notifies the Secretary that it has entered into two contracts.
Disclosure Form
The Patient Safety statute at 42 U.S.C. 299b-24(b)(1)(E) requires a
PSO to fully disclose information to the Secretary if the PSO has
additional financial, contractual, or reporting relationships with any
provider to which the PSO provides services pursuant to the Patient
Safety Act under contract or if the PSO is managed or controlled by, or
is not operated independently from, any of its contracting providers.
Disclosure forms will be collected only when a PSO has such
relationships with a contracting provider to report. The Secretary is
required to review each disclosure statement and make public findings
as to whether a PSO can fairly and accurately carry out its
responsibilities. AHRQ assumes that only a small percentage of entities
will need to file such disclosure forms. However, AHRQ is providing a
high estimate of 17 respondents annually and thus presumably
overestimating respondent burden. In summary, the annual burden of 8
hours for the collection of information requested by the disclosure
form is based upon the high estimate of 17 respondents per year and an
estimated 30 minutes per response. This information collection will
begin when a PS0 first reports having any of the specified types of
additional relationships with a health care provider with which it has
a contract to carry out patient safety activities.
PSO Information Form
Annual completion of a PSO information form will be voluntary and
will provide information to HHS on the type of healthcare settings that
PSOs are working with to carry out patient safety activities. This form
is designed to collect a minimum amount of data in order to gather
aggregate statistics on the reach of the Patient Safety Act with
respect to types of institutions participating and their general
location in the United States. This information will be included in
AHRQ's annual quality report, as required under section 923(c) of the
Patient Safety Act. No PSO-specific data will be released without PSO
consent. The overall annual burden estimate of 17 hours for the
collection of information requested by the PSO Information Form is
based upon an estimate of 33 respondents per year and an estimated 30
minutes per response. This information collection will begin toward the
end of the calendar year in which the first PSOs are listed by the
Secretary.
OCR Complaint Form
The complaint form will collect from individuals only the minimum
amount of information necessary for OCR to process and assess incoming
complaints. The overall annual burden estimate of 17 hours for the
collection of information requested by the underlying form is based
upon an estimate of 50 respondents per year and an estimated 20 minutes
per response. OCR's information collection using this form will not
begin until after there is at least one PSO receiving and generating
patient safety work product and there is an allegation of a violation
of the statutory protection of patient safety work product.
All Administrative Forms
The overall maximum anticipated annual burden estimate is 75 hours
for all the above described collections of information. Because the
forms filled out by PSOs vary over each of their first three years, the
table below includes three-year total estimates divided by three to
arrive at an annual estimate of burden hours. (See below.)
Exhibit 1.--Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of
Form Number of responses per Hours per Total burden
respondents respondent response hours
----------------------------------------------------------------------------------------------------------------
Patient Safety Organization Certification Form.. 100/3 1 30/60 17
Recertification Form*........................... 50/3 1 30/60 8
Disclosure Form................................. 50/3 1 30/60 8
Two-Contract Requirement Form**................. 100/3 1 15/60 8
Information Form***............................. 100/3 1 30/60 17
Patient Safety Confidentiality Complaint Form... 150/3 1 20/60 17
---------------------------------------------------------------
Total****................................... 500/3 na na 75
----------------------------------------------------------------------------------------------------------------
Note: * The Recertification Form will be completed by any interested PSO at least 45 days before the end of its
current three-year listing period. The three-year period for computing respondent burden begins with the date
when the approved forms are officially made available for submission. Thus the burden period does not
correspond exactly to the three-year period of listing. The burden period begins shortly (approximately 30
days) before any PSO's listing period. As a result, the burden for the first PSOs to submit certifications for
continued listing at least 45 days before their listing lapses is likely to fall just before the three-year
anniversary of their first burden, i.e. their completion of their initial certifications and before the end of
their third year of listing. We assume completing this form will require 30 minutes, the same time as for the
Certification Form. In the out-years, we expect the number of PSOs to remain stable, with the number of new
entrants offset by the number of entities that will relinquish their status or be revoked.
** The Two-Contract Requirement Form will be completed by each PSO within the 24-month period after initial
listing by the Secretary.
*** The Information Form will collect data by calendar year, beginning close to the end of the calendar year
when PSOs are first listed.
**** A total of 100 PSOs are expected to apply over three years: 50 in year 1; 25 in year 2; and 25 in year 3.
Relationship Disclosure, Two-Contract, and even voluntary Information Forms may be submitted by individual
PSOs in different years. OCR is anticipating considerable variation in the number of complaints per year.
Hence we have expressed the total for each year as the average of the expected total over the three year
collection period.
[[Page 21351]]
Exhibit 2.--Estimated Annualized Cost Burden
----------------------------------------------------------------------------------------------------------------
Average
Form Number of Total burden hourly wage Total cost
respondents hours rate burden
----------------------------------------------------------------------------------------------------------------
Patient Safety Organization Certification Form.. 100/3 17 $29.82 $506.94
Recertification Form............................ 50/3 8 29.82 238.56
Disclosure Form................................. 50/3 8 29.82 238.56
Two-Contract Requirement Form................... 100/3 8 29.82 506.94
Information Form................................ 100/3 17 29.82 506.94
Patient Safety Confidentiality Complaint Form... 150/3 17 29.82 506.94
---------------------------------------------------------------
Total....................................... 500/3 67 29.82 2,504.88
----------------------------------------------------------------------------------------------------------------
Estimated Annual Costs to the Federal Government
a. AHRQ
By statute, AHRQ must collect and review certifications from an
entity that seeks listing or continued listing as a PSO under the
Patient Safety Act. Additional information collection is also required
for entities to remain listed as a PSO (i.e., submissions regarding
compliance with the two-contract requirement and reports of certain
relationships between a PSO and each of its contracting providers). The
cost to AHRQ of processing the information collected with the above-
described forms is minimal; an estimated equivalent of only
approximately 0.05 FTE or $7,500 per year for each agency and virtually
no new overhead costs.
------------------------------------------------------------------------
Description Amount
------------------------------------------------------------------------
Personnel & Support Staff.................................... $7,500
Consultant (sub-contractor) services......................... 0
Equipment.................................................... 0
Supplies..................................................... 0
All other expenses........................................... 0
Average Annual Cost.......................................... 7,500
------------------------------------------------------------------------
b. OCR
OCR cannot conduct its work without collecting information through
its proposed complaint forms. Even if OCR did not use complaint forms
and only took information orally, it would still have to capture the
same information in order to begin processing a complaint. Therefore,
the incremental cost to OCR of processing the information collected
from the complaint form is minimal and is equivalent to only
approximately 0.05 FTE or $7,500 per year with, with virtually no new
overhead costs.
------------------------------------------------------------------------
Description Amount
------------------------------------------------------------------------
Personnel & Support Staff.................................... $7,500
Consultant (sub-contractor) services......................... 0
Equipment.................................................... 0
Supplies..................................................... 0
All other expenses........................................... 0
Average Annual Cost.......................................... 7,500
------------------------------------------------------------------------
Request for Comments
In accordance with the above-cited Paperwork Reduction Act
legislation, comments on the above-described AHRQ and OCR information
collection to implement the Patient Safety Act are requested with
regard to any of the following: (a) Whether the proposed collection of
information is necessary for the proper performance of AHRQ health care
research, quality improvement and information dissemination functions,
including whether the information will have practical utility; (b) the
accuracy of AHRQ's estimate of burden (including hours and costs) of
the proposed collection(s) of information; (c) ways to enhance the
quality, utility, and clarity of the information to be collected; and
(d) ways to minimize the burden of the collection of information upon
the respondents, including the use of automated collection techniques
or other forms of information technology.
Comments submitted in response to this notice will be summarized
and included in the Agency's subsequent request for OMB approval of the
proposed information collection.
All comments will become a matter of public record.
Dated: April 14, 2008.
Carolyn M. Clancy,
Director, AHRQ.
[FR Doc. E8-8440 Filed 4-18-08; 8:45 am]
BILLING CODE 4160-90-M