Agency Information Collection Activities: Proposed Collection: Public Comment Request, 72690-72692 [2014-28650]
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Federal Register / Vol. 79, No. 235 / Monday, December 8, 2014 / Notices
heading of this document. Received
comments may be seen in the Division
of Dockets Management between 9 a.m.
and 4 p.m., Monday through Friday, and
will be posted to the docket at https://
www.regulations.gov.
Dated: December 1, 2014.
Leslie Kux,
Associate Commissioner for Policy.
[FR Doc. 2014–28634 Filed 12–5–14; 8:45 am]
FOR FURTHER INFORMATION CONTACT:
BILLING CODE 4164–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2014–N–2031]
Request for Nominations on the Food
Advisory Committee
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
The Food and Drug
Administration (FDA) is requesting that
any industry organizations interested in
participating in the selection of a
nonvoting industry representative to
serve on the Food Advisory Committee
for the Center for Food Safety and
Applied Nutrition (CFSAN) notify FDA
in writing. FDA is also requesting
nominations for a nonvoting industry
representative(s) to serve on the Food
Advisory Committee. A nominee may
either be self-nominated or nominated
by an organization to serve as a
nonvoting industry representative.
Nominations will be accepted for
current vacancies effective with this
notice.
DATES: Any industry organization
interested in participating in the
selection of an appropriate nonvoting
member to represent industry interests
must send a letter stating that interest to
the FDA by January 7, 2015 (see
sections I and II of this document for
further details). Concurrently,
nomination materials for prospective
candidates should be sent to FDA by
January 7, 2015.
ADDRESSES: All statements of interest
from industry organizations interested
in participating in the selection process
of nonvoting industry representative
nomination should be sent to Karen
Strambler (see FOR FURTHER INFORMATION
CONTACT). All nominations for
nonvoting industry representatives may
be submitted electronically by accessing
the FDA Advisory Committee
Membership Nomination Portal: https://
www.accessdata.fda.gov/scripts/
FACTRSPortal/FACTRS/index.cfm or by
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SUMMARY:
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mail to Advisory Committee Oversight
and Management Staff, Food and Drug
Administration, 10903 New Hampshire
Ave., Bldg. 32, Rm. 5103, Silver Spring,
MD 20993–0002. Information about
becoming a member of an FDA advisory
committee can also be obtained by
visiting FDA’s Web site at https://
www.fda.gov/AdvisoryCommittees/
default.htm.
Karen Strambler, Office of Policy,
Regulations, and Social Science, Center
for Food Safety and Applied Nutrition,
5100 Paint Branch Pkwy., Rm. 1C–016,
College Park, MD 20740, 2400–402–
2589, karen.strambler@fda.hhs.gov.
SUPPLEMENTARY INFORMATION: The
Agency intends to add a nonvoting
industry representative(s) to the
following advisory committee:
I. CFSAN Advisory Committee, Food
Advisory Committee
The Committee reviews and evaluates
emerging food safety, nutrition and
other food- or cosmetic-related health
issues that FDA considers of primary
importance for its food and cosmetics
programs. The Committee may be
charged with reviewing and evaluating
available data and making
recommendations on matters such as
those relating to: (1) Broad scientific and
technical food- or cosmetic-related
issues; (2) the safety of food ingredients
and new foods; (3) labeling of foods and
cosmetics; (4) nutrient needs and
nutritional adequacy; and (5) safe
exposure limits for food contaminants.
The Committee may also be asked to
provide advice and make
recommendations on ways of
communicating to the public the
potential risks associated with these
issues and on approaches that might be
considered for addressing the issues.
II. Selection Procedure
Any industry organization interested
in participating in the selection of an
appropriate nonvoting member to
represent industry interests should send
a letter stating that interest to the FDA
contact (see FOR FURTHER INFORMATION
CONTACT) within 30 days of publication
of this document (see DATES). Within the
subsequent 30 days, FDA will send a
letter to each organization that has
expressed an interest, attaching a
complete list of all such organizations;
and a list of all nominees along with
´
´
their current resumes. The letter will
also state that it is the responsibility of
the interested organizations to confer
with one another and to select a
candidate, within 60 days after the
receipt of the FDA letter, to serve as the
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nonvoting member to represent industry
interests for the committee. The
interested organizations are not bound
by the list of nominees in selecting a
candidate. However, if no individual is
selected within 60 days, the
Commissioner will select the nonvoting
member to represent industry interests.
III. Application Procedure
Individuals may self-nominate and/or
an organization may nominate one or
more individuals to serve as a nonvoting
industry representative. Contact
information, a current curriculum vitae,
and the name of the committee of
interest should be sent to the FDA
Advisory Committee Membership
Nomination Portal (see ADDRESSES)
within 30 days of publication of this
document (see DATES). FDA will forward
all nominations to the organizations
expressing interest in participating in
the selection process for the committee.
(Persons who nominate themselves as
nonvoting industry representatives will
not participate in the selection process).
FDA seeks to include the views of
women, and men, members of all racial
and ethnic groups and individuals with
and without disabilities on its advisory
committees and, therefore encourages
nominations of appropriately qualified
candidates from these groups.
This notice is issued under the
Federal Advisory Committee Act (5
U.S.C. app. 2) and 21 CFR part 14,
relating to advisory committees.
Dated: December 1, 2014.
Jill Hartzler Warner,
Associate Commissioner for Special Medical
Programs.
[FR Doc. 2014–28652 Filed 12–5–14; 8:45 am]
BILLING CODE 4164–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Health Resources and Services
Administration
Agency Information Collection
Activities: Proposed Collection: Public
Comment Request
Health Resources and Services
Administration, HHS.
ACTION: Notice.
AGENCY:
In compliance with the
requirement for opportunity for public
comment on proposed data collection
projects (Section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995), the
Health Resources and Services
Administration (HRSA) announces
plans to submit an Information
Collection Request (ICR), described
SUMMARY:
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Federal Register / Vol. 79, No. 235 / Monday, December 8, 2014 / Notices
below, to the Office of Management and
Budget (OMB). Prior to submitting the
ICR to OMB, HRSA seeks comments
from the public regarding the burden
estimate, below, or any other aspect of
the ICR.
DATES: Comments on this Information
Collection Request must be received no
later than February 6, 2015.
ADDRESSES: Submit your comments to
paperwork@hrsa.gov or mail the HRSA
Information Collection Clearance
Officer, Room 10C–03, Parklawn
Building, 5600 Fishers Lane, Rockville,
MD 20857.
FOR FURTHER INFORMATION CONTACT: To
request more information on the
proposed project or to obtain a copy of
the data collection plans and draft
instruments, email paperwork@hrsa.gov
or call the HRSA Information Collection
Clearance Officer at (301) 443–1984.
SUPPLEMENTARY INFORMATION: When
submitting comments or requesting
information, please include the
information request collection title for
reference.
Information Collection Request Title:
National Practitioner Data Bank for
Adverse Information on Physicians and
Other Health Care Practitioners—45
CFR part 60 Regulations and Forms
OMB No. 0915–0126—Revision
Abstract: This is a request for a
revision of OMB approval of the
information collection contained in
regulations found at 45 CFR part 60
governing the National Practitioner Data
Bank (NPDB) and the forms to be used
in registering with, reporting
information to, and requesting
information from the NPDB.
Administrative forms are also included
to aid in monitoring compliance with
federal reporting and querying
requirements. Responsibility for NPDB
implementation and operation resides
in the Bureau of Health Workforce,
Health Resources and Services
Administration (HRSA), Department of
Health and Human Services (HHS).
The intent of the NPDB is to improve
the quality of health care by
encouraging hospitals, state licensing
boards, professional societies, and other
entities providing health care services to
identify and discipline those who
engage in unprofessional behavior, and
to restrict the ability of incompetent
health care practitioners, providers, or
suppliers to move from state to state
without disclosure of previous
damaging or incompetent performance.
It also serves as a fraud and abuse
clearinghouse for the reporting and
disclosing of certain final adverse
actions (excluding settlements in which
no findings of liability have been made)
taken against health care practitioners,
providers, or suppliers by health plans,
federal agencies, and state agencies.
The reporting forms, request for
information forms (query forms), and
administrative forms (used to monitor
compliance) are accessed, completed,
and submitted to the NPDB
electronically through the NPDB Web
site at https://www.npdb.hrsa.gov/. All
reporting and querying is performed
through this secure Web site.
Need and Proposed Use of the
Information: The NPDB acts primarily
as a flagging system; its principal
purpose is to facilitate comprehensive
review of practitioners’ professional
credentials and background.
Information is collected from, and
disseminated to, eligible entities
(entities that are entitled to query and/
or report to the NPDB as authorized in
Title 45 part 60 of the Code of Federal
Regulations) on the following: (1)
Medical malpractice payments, (2)
licensure actions taken by Boards of
Medical Examiners, (3) state licensure
and certification actions, (4) federal
licensure and certification actions, (5)
negative actions or findings taken by
peer review organizations or private
accreditation entities, (6) adverse
actions taken against clinical privileges,
(7) federal or state criminal convictions
related to the delivery of a health care
item or service, (8) civil judgments
related to the delivery of a health care
item or service, (9) exclusions from
participation in federal or state health
care programs, and (10) other
adjudicated actions or decisions. It is
intended that NPDB information should
be considered with other relevant
information in evaluating credentials of
health care practitioners, providers, and
suppliers.
Likely Respondents: Eligible entities
that are entitled to query and/or report
to the NPDB as authorized in
regulations found at 45 CFR part 60.
Burden Statement: Burden in this
context means the time expended by
persons to generate, maintain, retain,
disclose or provide the information
requested. This includes the time
needed to review instructions; to
develop, acquire, install and utilize
technology and systems for the purpose
of collecting, validating and verifying
information, processing and
maintaining information, and disclosing
and providing information; to train
personnel and to be able to respond to
a collection of information; to search
data sources; to complete and review
the collection of information; and to
transmit or otherwise disclose the
information. The total annual burden
hours estimated for this Information
Collection Request are summarized in
the table below.
TOTAL ESTIMATED ANNUALIZED BURDEN HOURS
Responses
per
respondent
Number of
respondents
Total
responses
Average
burden per
response
(in hours)
Total burden
hours
Regulation citation
Form name
§ 60.6: Reporting errors, omissions,
revisions or whether an action is on
appeal.
Correction, Revision to Action, Correction of Revision to Action, Void,
Notice of Appeal (manual).
Correction, Revision to Action, Correction of Revision to Action, Void,
Notice of Appeal (automated).
Medical Malpractice Payment (manual).
Medical Malpractice Payment (automated).
State Licensure (manual) ....................
State Licensure (automated) ..............
20,482
1
20,482
.25
5,121
17,185
1
17,185
.0003
5
12,613
1
12,613
.75
9,460
250
1
250
.0003
.1
16,770
17,422
1
1
16,770
17,422
.75
.0003
12,578
5
DEA/Federal Licensure .......................
114
1
114
.75
86
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§ 60.7: Reporting medical malpractice
payments.
§ 60.8: Reporting licensure actions
taken by Boards of Medical Examiners & § 60.9: Reporting licensure
and certification actions taken by
States.
§ 60.10: Reporting Federal licensure
and certification actions.
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TOTAL ESTIMATED ANNUALIZED BURDEN HOURS—Continued
Responses
per
respondent
Number of
respondents
Total
responses
Average
burden per
response
(in hours)
Total burden
hours
Regulation citation
Form name
§ 60.11: Reporting negative actions or
findings taken by peer review organizations or private accreditation entities.
§ 60.12: Reporting adverse actions
taken against clinical privileges.
§ 60.13: Reporting Federal or State
criminal convictions related to the
delivery of a health care item or
service.
Peer Review Organization ..................
Accreditation .......................................
10
12
1
1
10
12
.75
.75
8
9
Title IV Clinical Privileges Actions ......
Professional Society ...........................
Criminal Conviction (Guilty Plea or
Trial) (manual).
Criminal Conviction (Guilty Plea or
Trial) (automated).
Deferred Conviction or Pre-Trial Diversion.
Nolo Contendere (No Contest) Plea ...
Injunction .............................................
Civil Judgment ....................................
671
50
1,308
937
1
1
1
1
671
50
1,308
937
.75
.75
.75
.0003
503
38
981
.3
50
1
50
.75
38
80
10
14
1
1
1
80
10
14
.75
.75
.75
60
8
11
Exclusion/Debarment (manual) ...........
Exclusion/Debarment (automated) .....
1,185
5,094
1
1
1,185
5,094
.75
.0003
889
2
Government Administrative .................
Health Plan Action ..............................
One Time Query for an Individual
(manual).
One Time Query for an Individual
(automated).
One Time Query for an Organization
(manual).
One Time Query for an Organization
(automated).
Self-Query on an Individual ................
Self-Query on an Organization ...........
Continuous Query (manual) ................
Continuous Query (automated) ..........
Subject Statement and Dispute ..........
Request for Dispute Resolution ..........
Non-Hospital Entity Registration (Initial).
Non-Hospital Entity Registration (Renewal & Update).
Hospital Registration (Initial) ...............
Hospital Registration (Renewal & Update).
Licensing Board Data Request ...........
Reporting Entity Discrepancy Letter ...
Licensing Board Attestation ................
Corrective Action Plan ........................
Reconciling Missing Actions ...............
Agent Registration (Initial) ..................
Agent Registration (Renewal & Update).
Electronic Transfer of Funds (EFT)
Authorization.
Authorized Agent Designation ............
Account Discrepancy ..........................
2,233
524
1,980,825
1
1
1
2,233
524
1,980,825
.75
.75
.08
1,675
393
158,466
2,163,208
1
2,163,208
.0003
649
39,920
1
39,920
.08
3,194
2,266
1
2,266
.0003
1
77,318
427
508,203
121,718
3,501
94
524
1
1
1
1
1
1
1
77,318
427
508,203
121,718
3,501
94
524
.42
.42
.08
.0003
.75
8
1
30,201
167
40,656
37
2,626
752
524
6,383
1
6,383
.25
1,596
37
3,198
1
1
37
3,198
1
.25
37
800
140
389
354
10
2,176
30
194
1
1
1
1
1
1
1
140
389
354
10
2,176
30
194
10.5
4
1
.08
.08
1
.08
1,470
1556
354
1
174
30
16
566
1
566
.08
45
788
41
1
1
788
41
.25
.25
197
10
5,009,324
........................
5,009,324
........................
275,429
§ 60.14: Reporting civil judgments related to the delivery of a health care
item or service.
§ 60.15: Reporting exclusions from
participation in Federal or State
health care programs.
§ 60.16: Reporting other adjudicated
actions or decisions.
§ 60.18 Requesting Information from
the NPDB.
§ 60.21: How to dispute the accuracy
of NPDB information.
Administrative ......................................
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Total .............................................
.............................................................
HRSA specifically requests comments
on (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.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Jackie Painter,
Acting Director, Division of Policy and
Information Coordination.
National Institutes of Health
[FR Doc. 2014–28650 Filed 12–5–14; 8:45 am]
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Expert Panel Meeting on Identifying
Research Needs for Assessing Safe
Use of High Intakes of Folic Acid;
Notice of Public Meeting and
Registration Information
The National Toxicology
Program (NTP) and the Office of Dietary
Supplements (ODS) announce a public
expert panel meeting on May 11–12,
SUMMARY:
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08DEN1
]]>Agencies
[Federal Register Volume 79, Number 235 (Monday, December 8, 2014)]
[Proposed Rules]
[Pages 72690-72692]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2014-28650]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Health Resources and Services Administration
Agency Information Collection Activities: Proposed Collection:
Public Comment Request
AGENCY: Health Resources and Services Administration, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: In compliance with the requirement for opportunity for public
comment on proposed data collection projects (Section 3506(c)(2)(A) of
the Paperwork Reduction Act of 1995), the Health Resources and Services
Administration (HRSA) announces plans to submit an Information
Collection Request (ICR), described
[[Page 72691]]
below, to the Office of Management and Budget (OMB). Prior to
submitting the ICR to OMB, HRSA seeks comments from the public
regarding the burden estimate, below, or any other aspect of the ICR.
DATES: Comments on this Information Collection Request must be received
no later than February 6, 2015.
ADDRESSES: Submit your comments to paperwork@hrsa.gov or mail the HRSA
Information Collection Clearance Officer, Room 10C-03, Parklawn
Building, 5600 Fishers Lane, Rockville, MD 20857.
FOR FURTHER INFORMATION CONTACT: To request more information on the
proposed project or to obtain a copy of the data collection plans and
draft instruments, email paperwork@hrsa.gov or call the HRSA
Information Collection Clearance Officer at (301) 443-1984.
SUPPLEMENTARY INFORMATION: When submitting comments or requesting
information, please include the information request collection title
for reference.
Information Collection Request Title: National Practitioner Data
Bank for Adverse Information on Physicians and Other Health Care
Practitioners--45 CFR part 60 Regulations and Forms OMB No. 0915-0126--
Revision
Abstract: This is a request for a revision of OMB approval of the
information collection contained in regulations found at 45 CFR part 60
governing the National Practitioner Data Bank (NPDB) and the forms to
be used in registering with, reporting information to, and requesting
information from the NPDB. Administrative forms are also included to
aid in monitoring compliance with federal reporting and querying
requirements. Responsibility for NPDB implementation and operation
resides in the Bureau of Health Workforce, Health Resources and
Services Administration (HRSA), Department of Health and Human Services
(HHS).
The intent of the NPDB is to improve the quality of health care by
encouraging hospitals, state licensing boards, professional societies,
and other entities providing health care services to identify and
discipline those who engage in unprofessional behavior, and to restrict
the ability of incompetent health care practitioners, providers, or
suppliers to move from state to state without disclosure of previous
damaging or incompetent performance. It also serves as a fraud and
abuse clearinghouse for the reporting and disclosing of certain final
adverse actions (excluding settlements in which no findings of
liability have been made) taken against health care practitioners,
providers, or suppliers by health plans, federal agencies, and state
agencies.
The reporting forms, request for information forms (query forms),
and administrative forms (used to monitor compliance) are accessed,
completed, and submitted to the NPDB electronically through the NPDB
Web site at https://www.npdb.hrsa.gov/. All reporting and querying is
performed through this secure Web site.
Need and Proposed Use of the Information: The NPDB acts primarily
as a flagging system; its principal purpose is to facilitate
comprehensive review of practitioners' professional credentials and
background. Information is collected from, and disseminated to,
eligible entities (entities that are entitled to query and/or report to
the NPDB as authorized in Title 45 part 60 of the Code of Federal
Regulations) on the following: (1) Medical malpractice payments, (2)
licensure actions taken by Boards of Medical Examiners, (3) state
licensure and certification actions, (4) federal licensure and
certification actions, (5) negative actions or findings taken by peer
review organizations or private accreditation entities, (6) adverse
actions taken against clinical privileges, (7) federal or state
criminal convictions related to the delivery of a health care item or
service, (8) civil judgments related to the delivery of a health care
item or service, (9) exclusions from participation in federal or state
health care programs, and (10) other adjudicated actions or decisions.
It is intended that NPDB information should be considered with other
relevant information in evaluating credentials of health care
practitioners, providers, and suppliers.
Likely Respondents: Eligible entities that are entitled to query
and/or report to the NPDB as authorized in regulations found at 45 CFR
part 60.
Burden Statement: Burden in this context means the time expended by
persons to generate, maintain, retain, disclose or provide the
information requested. This includes the time needed to review
instructions; to develop, acquire, install and utilize technology and
systems for the purpose of collecting, validating and verifying
information, processing and maintaining information, and disclosing and
providing information; to train personnel and to be able to respond to
a collection of information; to search data sources; to complete and
review the collection of information; and to transmit or otherwise
disclose the information. The total annual burden hours estimated for
this Information Collection Request are summarized in the table below.
Total Estimated Annualized Burden Hours
--------------------------------------------------------------------------------------------------------------------------------------------------------
Average
Number of Responses per Total burden per Total burden
Regulation citation Form name respondents respondent responses response (in hours
hours)
--------------------------------------------------------------------------------------------------------------------------------------------------------
Sec. 60.6: Reporting errors, Correction, Revision to Action, 20,482 1 20,482 .25 5,121
omissions, revisions or whether an Correction of Revision to
action is on appeal. Action, Void, Notice of Appeal
(manual).
Correction, Revision to Action, 17,185 1 17,185 .0003 5
Correction of Revision to
Action, Void, Notice of Appeal
(automated).
Sec. 60.7: Reporting medical Medical Malpractice Payment 12,613 1 12,613 .75 9,460
malpractice payments. (manual).
Medical Malpractice Payment 250 1 250 .0003 .1
(automated).
Sec. 60.8: Reporting licensure State Licensure (manual)....... 16,770 1 16,770 .75 12,578
actions taken by Boards of Medical State Licensure (automated).... 17,422 1 17,422 .0003 5
Examiners & Sec. 60.9: Reporting
licensure and certification actions
taken by States.
Sec. 60.10: Reporting Federal DEA/Federal Licensure.......... 114 1 114 .75 86
licensure and certification actions.
[[Page 72692]]
Sec. 60.11: Reporting negative Peer Review Organization....... 10 1 10 .75 8
actions or findings taken by peer Accreditation.................. 12 1 12 .75 9
review organizations or private
accreditation entities.
Sec. 60.12: Reporting adverse actions Title IV Clinical Privileges 671 1 671 .75 503
taken against clinical privileges. Actions. 50 1 50 .75 38
Professional Society...........
Sec. 60.13: Reporting Federal or Criminal Conviction (Guilty 1,308 1 1,308 .75 981
State criminal convictions related to Plea or Trial) (manual). 937 1 937 .0003 .3
the delivery of a health care item or Criminal Conviction (Guilty
service. Plea or Trial) (automated).
Deferred Conviction or Pre- 50 1 50 .75 38
Trial Diversion.
Nolo Contendere (No Contest) 80 1 80 .75 60
Plea.
Injunction..................... 10 1 10 .75 8
Sec. 60.14: Reporting civil judgments Civil Judgment................. 14 1 14 .75 11
related to the delivery of a health
care item or service.
Sec. 60.15: Reporting exclusions from Exclusion/Debarment (manual)... 1,185 1 1,185 .75 889
participation in Federal or State Exclusion/Debarment (automated) 5,094 1 5,094 .0003 2
health care programs.
Sec. 60.16: Reporting other Government Administrative...... 2,233 1 2,233 .75 1,675
adjudicated actions or decisions. Health Plan Action............. 524 1 524 .75 393
Sec. 60.18 Requesting Information One Time Query for an 1,980,825 1 1,980,825 .08 158,466
from the NPDB. Individual (manual).
One Time Query for an 2,163,208 1 2,163,208 .0003 649
Individual (automated).
One Time Query for an 39,920 1 39,920 .08 3,194
Organization (manual).
One Time Query for an 2,266 1 2,266 .0003 1
Organization (automated).
Self-Query on an Individual.... 77,318 1 77,318 .42 30,201
Self-Query on an Organization.. 427 1 427 .42 167
Continuous Query (manual)...... 508,203 1 508,203 .08 40,656
Continuous Query (automated)... 121,718 1 121,718 .0003 37
Sec. 60.21: How to dispute the Subject Statement and Dispute.. 3,501 1 3,501 .75 2,626
accuracy of NPDB information. Request for Dispute Resolution. 94 1 94 8 752
Administrative......................... Non-Hospital Entity 524 1 524 1 524
Registration (Initial).
Non-Hospital Entity 6,383 1 6,383 .25 1,596
Registration (Renewal &
Update).
Hospital Registration (Initial) 37 1 37 1 37
Hospital Registration (Renewal 3,198 1 3,198 .25 800
& Update).
Licensing Board Data Request... 140 1 140 10.5 1,470
Reporting Entity Discrepancy 389 1 389 4 1556
Letter.
Licensing Board Attestation.... 354 1 354 1 354
Corrective Action Plan......... 10 1 10 .08 1
Reconciling Missing Actions.... 2,176 1 2,176 .08 174
Agent Registration (Initial)... 30 1 30 1 30
Agent Registration (Renewal & 194 1 194 .08 16
Update).
Electronic Transfer of Funds 566 1 566 .08 45
(EFT) Authorization.
Authorized Agent Designation... 788 1 788 .25 197
Account Discrepancy............ 41 1 41 .25 10
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Total.............................. ............................... 5,009,324 .............. 5,009,324 .............. 275,429
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HRSA specifically requests comments on (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.
Jackie Painter,
Acting Director, Division of Policy and Information Coordination.
[FR Doc. 2014-28650 Filed 12-5-14; 8:45 am]
BILLING CODE 4165-15-P
