Agency Information Collection Activities: Proposed Collection: Public Comment Request; 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, 42821-42823 [2017-19252]
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Federal Register / Vol. 82, No. 175 / Tuesday, September 12, 2017 / Notices
Studies.’’ It does not establish any rights
for any person and is not binding on
FDA or the public. You can use an
alternative approach if it satisfies the
requirements of the applicable statutes
and regulations. This guidance is not
subject to Executive Order 12866.
III. Electronic Access
Persons interested in obtaining a copy
of the guidance may do so by
downloading an electronic copy from
the internet. A search capability for all
Center for Devices and Radiological
Health guidance documents is available
at https://www.fda.gov/MedicalDevices/
DeviceRegulationandGuidance/
GuidanceDocuments/default.htm.
Guidance documents are also available
at https://www.fda.gov/BiologicsBlood
Vaccines/GuidanceCompliance
RegulatoryInformation/default.htm or
https://www.regulations.gov. Persons
unable to download an electronic copy
of ‘‘Evaluation and Reporting of Age,
Race, and Ethnicity Data in Medical
Device Clinical Studies’’ may send an
email request to CDRH-Guidance@
fda.hhs.gov to receive an electronic
copy of the document. Please use the
document number 1500626 to identify
the guidance you are requesting.
pmangrum on DSK3GDR082PROD with NOTICES1
IV. Paperwork Reduction Act of 1995
This guidance refers to previously
approved collections of information
found in FDA regulations. These
collections of information are subject to
review by the Office of Management and
Budget (OMB) under the Paperwork
Reduction Act of 1995 (44 U.S.C. 3501–
3520). These collections of information
in 21 CFR part 812 have been approved
under OMB control number 0910–0078;
the collections of information in 21 CFR
part 807, subpart E, have been approved
under OMB control number 0910–0120;
the collections of information in 21 CFR
part 814, subparts A through E, have
been approved under OMB control
number 0910–0231; the collections of
information in 21 CFR part 814, subpart
H, have been approved under OMB
control number 0910–0332; the
collections of information in 21 CFR
part 822 have been approved under
OMB control number 0910–0449; and
the collections of information in 21 CFR
part 801 have been approved under
OMB control number 0910–0485.
V. References
The following references are on
display in the Dockets Management
Staff office (see ADDRESSES) and are
available for viewing by interested
persons between 9 a.m. and 4 p.m.,
Monday through Friday; they are also
available electronically at https://
VerDate Sep<11>2014
15:19 Sep 11, 2017
Jkt 241001
www.regulations.gov. FDA has verified
the Web site addresses, as of the date
this document publishes in the Federal
Register, but Web sites are subject to
change over time.
1. FDA Report: Collection, Analysis, and
Availability of Demographic Subgroup
Data for FDA-Approved Medical
Products, issued August 2013, required
under FDASIA section 907, available at
https://www.fda.gov/downloads/
RegulatoryInformation/Legislation/
SignificantAmendmentstotheFDCAct/
FDASIA/UCM365544.pdf.
2. FDA’s Action Plan to Enhance the
Collection and Availability of
Demographic Subgroup Data (August,
2014), available at https://www.fda.gov/
downloads/RegulatoryInformation/
Legislation/
SignificantAmendmentstotheFDCAct/
FDASIA/UCM410474.pdf.
3. FDA’s guidance entitled ‘‘Evaluation of
Sex-Specific Data in Medical Device
Clinical Studies’’ (August 22, 2014),
available at https://www.fda.gov/
downloads/MedicalDevices/Device
RegulationandGuidance/Guidance
Documents/UCM283707.pdf.
Dated: September 7, 2017.
Leslie Kux,
Associate Commissioner for Policy.
[FR Doc. 2017–19259 Filed 9–11–17; 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; 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
Health Resources and Services
Administration (HRSA), Department of
Health and Human Services (HHS).
AGENCY:
ACTION:
Notice.
In compliance with the
requirement for opportunity for public
comment on proposed data collection
projects of the Paperwork Reduction Act
of 1995, HRSA announces plans to
submit an Information Collection
Request (ICR), described 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.
SUMMARY:
PO 00000
Frm 00041
Fmt 4703
Sfmt 4703
42821
Comments on this ICR must be
received no later than November 13,
2017.
ADDRESSES: Submit your comments to
paperwork@hrsa.gov or mail to the
HRSA Information Collection Clearance
Officer, 14N39, 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, in compliance with Section
3506(c)(2)(A) of the Paperwork
Reduction Act of 1995.
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 HRSA’s Bureau of Health Workforce.
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
DATES:
E:\FR\FM\12SEN1.SGM
12SEN1
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Federal Register / Vol. 82, No. 175 / Tuesday, September 12, 2017 / Notices
electronically through the NPDB Web
site at https://www.npdb.hrsa.gov/. All
reporting and querying is performed
through the secure portal of this Web
site. This revision proposes changes to
eliminate redundant and unnecessary
forms, improve user error recovery, and
improve overall data integrity. There is
no change to the average burden per
response. The total estimated number of
respondents has increased from 5
million in 2015 to over 6 million in
2017, primarily attributable to increases
in use of the ‘‘One-Time Query for an
Individual’’ and ‘‘Continuous Query’’
forms. The increase in total respondents
has resulted in an estimated increase of
approximately 47,000 total burden
hours.
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 CFR 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
or individuals 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 ICR are
summarized in the table below.
TOTAL ESTIMATED ANNUALIZED BURDEN HOURS
pmangrum on DSK3GDR082PROD with NOTICES1
Accreditation ......................................................................
Civil Judgment ...................................................................
Criminal Conviction (Guilty Plea or Trial) (manual) ...........
Criminal Conviction (Guilty Plea or Trial) (automated) ......
DEA/Federal Licensure ......................................................
Deferred Conviction or Pre-Trial Diversion ........................
Exclusion/Debarment (manual) ..........................................
Exclusion/Debarment (automated) ....................................
Government Administrative ................................................
Health Plan Action .............................................................
Injunction ............................................................................
Medical Malpractice Payment (manual) ............................
Medical Malpractice Payment (automated) .......................
Nolo Contendere (No Contest) Plea ..................................
Peer Review Organization .................................................
Professional Society ..........................................................
State Licensure (manual) ...................................................
State Licensure (automated) .............................................
Title IV Clinical Privileges Actions .....................................
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) ...................
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) ...........
Continuous Query (manual) ...............................................
Continuous Query (automated) .........................................
Self-Query on an Individual ...............................................
Self-Query on an Organization ..........................................
Entity Registration (Initial) ..................................................
Entity Registration (Renewal & Update) ............................
Agent Registration (Initial) .................................................
Agent Registration (Renewal & Update) ...........................
Entity Profile .......................................................................
Licensing Board Attestation ...............................................
Licensing Board Data Request ..........................................
Reconciling Missing Actions ..............................................
Corrective Action Plan .......................................................
VerDate Sep<11>2014
15:19 Sep 11, 2017
Jkt 241001
Number of
responses per
respondent
Number of
respondents
Form name
PO 00000
Frm 00042
Total
responses
Average burden
per response
(in hours)
Total burden
hours
(rounded up)
10
10
1,140
688
698
54
1,624
3,180
2,062
335
10
11,993
242
85
10
49
19,160
25,980
698
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
10
10
1,140
688
698
54
1,624
3,180
2,062
335
10
11,993
242
85
10
49
19,160
25,980
698
.75
.75
.75
.0003
.75
.75
.75
.0003
.75
.75
.75
.75
.0003
.75
.75
.75
.75
.0003
.75
8
8
855
1
524
41
1,218
1
1,547
252
8
8,995
1
64
8
37
14,370
8
524
11,114
1
11,114
.25
2,779
17,966
2,054,381
2,813,341
39,695
10,201
643,860
226,838
131,481
1,545
1,073
14,060
85
278
9,000
301
146
7,981
10
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
17,966
2,054,381
2,813,341
39,695
10,201
643,860
226,838
131,481
1,545
1,073
14,060
85
278
9,000
301
146
7,981
10
.0003
.08
.0003
.08
.0003
.08
.0003
.42
.42
1
.25
1
.08
.25
1
10.5
0.8
.08
6
164,351
844
3,176
4
51,509
69
55,223
649
1,073
3,515
85
23
2,250
301
1,533
6,385
1
Fmt 4703
Sfmt 4703
E:\FR\FM\12SEN1.SGM
12SEN1
42823
Federal Register / Vol. 82, No. 175 / Tuesday, September 12, 2017 / Notices
TOTAL ESTIMATED ANNUALIZED BURDEN HOURS—Continued
Number of
responses per
respondent
Number of
respondents
Form name
Total
responses
Average burden
per response
(in hours)
Total burden
hours
(rounded up)
Missing Report Form .........................................................
Subject Statement and Dispute .........................................
Request for Dispute Resolution .........................................
Electronic Transfer of Funds (EFT) Authorization .............
Authorized Agent Designation ...........................................
Account Discrepancy .........................................................
New Administrator Request ...............................................
Query Credit Purchase ......................................................
Educational Request ..........................................................
Account Balance Transfer .................................................
29
3,547
99
654
213
10
3,016
789
10
10
1
1
1
1
1
1
1
1
1
1
29
3,547
99
654
213
10
3,016
789
10
10
.08
.75
8
.08
.25
.25
.08
.08
.08
.08
3
2,661
792
53
54
3
242
64
1
1
Total ............................................................................
6,059,761
........................
6,059,761
..........................
326,120
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.
Amy McNulty,
Acting Director, Division of the Executive
Secretariat.
[FR Doc. 2017–19252 Filed 9–11–17; 8:45 am]
BILLING CODE 4165–15–P
Dated: September 6, 2017.
Michelle Trout,
Program Analyst, Office of Federal Advisory
Committee Policy.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
[FR Doc. 2017–19232 Filed 9–11–17; 8:45 am]
pmangrum on DSK3GDR082PROD with NOTICES1
Eunice Kennedy Shriver National
Institute of Child Health and Human
Development; Notice of Closed
Meeting
BILLING CODE 4140–01–P
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended, notice is hereby given of the
following meeting.
The meeting will be closed to the
public in accordance with the
provisions set forth in sections
552b(c)(4) and 552b(c)(6), Title 5 U.S.C.,
as amended. The grant applications and
the discussions could disclose
confidential trade secrets or commercial
property such as patentable material,
and personal information concerning
individuals associated with the grant
applications, the disclosure of which
would constitute a clearly unwarranted
invasion of personal privacy.
Name of Committee: National Institute of
Child Health and Human Development Initial
Review Group; Developmental Biology
Subcommittee.
VerDate Sep<11>2014
15:19 Sep 11, 2017
Jkt 241001
Date: October 2, 2017.
Time: 8:00 a.m. to 6:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: Residence Inn Bethesda Downtown,
7335 Wisconsin Ave., Bethesda, MD 20814.
Contact Person: Cathy J. Wedeen, Ph.D.,
Scientific Review Officer, Division of
Scientific Review, OD, Eunice Kennedy
Shriver National Institute of Child Health
and Human Development, NIH, DHHS, 6710
B Rockledge Drive, Bethesda, Maryland
20892, 301–435–6878, wedeenc@
mail.nih.gov.
(Catalogue of Federal Domestic Assistance
Program Nos. 93.864, Population Research;
93.865, Research for Mothers and Children;
93.929, Center for Medical Rehabilitation
Research; 93.209, Contraception and
Infertility Loan Repayment Program, National
Institutes of Health, HHS)
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Government-Owned Inventions;
Availability for Licensing
AGENCY:
National Institutes of Health,
HHS.
ACTION:
Notice.
Government owned
intellectual property covering imaging
agents with improved renal clearance
available for licensing and
commercialization.
FOR FURTHER INFORMATION CONTACT:
Licensing information and copies of the
patent applications listed below may be
obtained by emailing the indicated
licensing contact at the National Heart,
Lung, and Blood, Office of Technology
SUMMARY:
PO 00000
Frm 00043
Fmt 4703
Sfmt 4703
Transfer and Development Office of
Technology Transfer, 31 Center Drive,
Room 4A29, MSC2479, Bethesda, MD
20892–2479; telephone: 301–402–5579.
A signed Confidential Disclosure
Agreement may be required to receive
copies of the patent applications.
SUPPLEMENTARY INFORMATION: The
inventions listed below are owned by an
agency of the U.S. Government and are
available for licensing in the U.S. in
accordance with 35 U.S.C. 209 and 37
CFR part 404 to achieve expeditious
commercialization of results of
federally-funded research and
development. Foreign patent
applications are filed on selected
inventions to extend market coverage
for companies and may also be available
for licensing. A description of the
technology available for licensing
follows.
Evans Blue Dye Derivatives for Serum
Albumin Labeling
Description of Technology: The
invention is an imaging agent and
method of its use for imaging blood
pools and the lymphatic system. The
imaging agent binds with high affinity
to serum albumin, the most abundant
serum protein, and can be tagged with
several isotopes making it suitable for
magnetic resonance imaging or positron
emission tomographic imaging. To date,
only very few blood-pool tracers have
been introduced for positron emission
tomography. The existing ones have
short half-lives (20.4 min for 11C and
2.05 min for 15O) and thus can only be
used in centers with an in-house
cyclotron. Compared with these
radiometals, 18F has the advantages of
being a pure position emitter with ideal
half-life. It is the dominant radioisotope
used for PET imaging for both clinical
applications and preclinical
investigations. Evans blue dye has been
an important tool in many physiological
and clinical investigations because of its
E:\FR\FM\12SEN1.SGM
12SEN1
]]>Agencies
[Federal Register Volume 82, Number 175 (Tuesday, September 12, 2017)]
[Notices]
[Pages 42821-42823]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2017-19252]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Health Resources and Services Administration
Agency Information Collection Activities: Proposed Collection:
Public Comment Request; 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
AGENCY: Health Resources and Services Administration (HRSA), Department
of Health and Human Services (HHS).
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: In compliance with the requirement for opportunity for public
comment on proposed data collection projects of the Paperwork Reduction
Act of 1995, HRSA announces plans to submit an Information Collection
Request (ICR), described 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 ICR must be received no later than November 13,
2017.
ADDRESSES: Submit your comments to paperwork@hrsa.gov or mail to the
HRSA Information Collection Clearance Officer, 14N39, 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, in compliance with Section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995.
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 HRSA's Bureau of Health Workforce.
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
[[Page 42822]]
electronically through the NPDB Web site at https://www.npdb.hrsa.gov/.
All reporting and querying is performed through the secure portal of
this Web site. This revision proposes changes to eliminate redundant
and unnecessary forms, improve user error recovery, and improve overall
data integrity. There is no change to the average burden per response.
The total estimated number of respondents has increased from 5 million
in 2015 to over 6 million in 2017, primarily attributable to increases
in use of the ``One-Time Query for an Individual'' and ``Continuous
Query'' forms. The increase in total respondents has resulted in an
estimated increase of approximately 47,000 total burden hours.
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 CFR 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 or individuals 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 ICR are summarized in the table below.
Total Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Average burden Total burden
Form name Number of responses per Total per response hours (rounded
respondents respondent responses (in hours) up)
----------------------------------------------------------------------------------------------------------------
Accreditation.................. 10 1 10 .75 8
Civil Judgment................. 10 1 10 .75 8
Criminal Conviction (Guilty 1,140 1 1,140 .75 855
Plea or Trial) (manual).......
Criminal Conviction (Guilty 688 1 688 .0003 1
Plea or Trial) (automated)....
DEA/Federal Licensure.......... 698 1 698 .75 524
Deferred Conviction or Pre- 54 1 54 .75 41
Trial Diversion...............
Exclusion/Debarment (manual)... 1,624 1 1,624 .75 1,218
Exclusion/Debarment (automated) 3,180 1 3,180 .0003 1
Government Administrative...... 2,062 1 2,062 .75 1,547
Health Plan Action............. 335 1 335 .75 252
Injunction..................... 10 1 10 .75 8
Medical Malpractice Payment 11,993 1 11,993 .75 8,995
(manual)......................
Medical Malpractice Payment 242 1 242 .0003 1
(automated)...................
Nolo Contendere (No Contest) 85 1 85 .75 64
Plea..........................
Peer Review Organization....... 10 1 10 .75 8
Professional Society........... 49 1 49 .75 37
State Licensure (manual)....... 19,160 1 19,160 .75 14,370
State Licensure (automated).... 25,980 1 25,980 .0003 8
Title IV Clinical Privileges 698 1 698 .75 524
Actions.......................
Correction, Revision to Action, 11,114 1 11,114 .25 2,779
Correction of Revision to
Action, Void, Notice of Appeal
(manual)......................
Correction, Revision to Action, 17,966 1 17,966 .0003 6
Correction of Revision to
Action, Void, Notice of Appeal
(automated)...................
One-Time Query for an 2,054,381 1 2,054,381 .08 164,351
Individual (manual)...........
One-Time Query for an 2,813,341 1 2,813,341 .0003 844
Individual (automated)........
One-Time Query for an 39,695 1 39,695 .08 3,176
Organization (manual).........
One-Time Query for an 10,201 1 10,201 .0003 4
Organization (automated)......
Continuous Query (manual)...... 643,860 1 643,860 .08 51,509
Continuous Query (automated)... 226,838 1 226,838 .0003 69
Self-Query on an Individual.... 131,481 1 131,481 .42 55,223
Self-Query on an Organization.. 1,545 1 1,545 .42 649
Entity Registration (Initial).. 1,073 1 1,073 1 1,073
Entity Registration (Renewal & 14,060 1 14,060 .25 3,515
Update).......................
Agent Registration (Initial)... 85 1 85 1 85
Agent Registration (Renewal & 278 1 278 .08 23
Update).......................
Entity Profile................. 9,000 1 9,000 .25 2,250
Licensing Board Attestation.... 301 1 301 1 301
Licensing Board Data Request... 146 1 146 10.5 1,533
Reconciling Missing Actions.... 7,981 1 7,981 0.8 6,385
Corrective Action Plan......... 10 1 10 .08 1
[[Page 42823]]
Missing Report Form............ 29 1 29 .08 3
Subject Statement and Dispute.. 3,547 1 3,547 .75 2,661
Request for Dispute Resolution. 99 1 99 8 792
Electronic Transfer of Funds 654 1 654 .08 53
(EFT) Authorization...........
Authorized Agent Designation... 213 1 213 .25 54
Account Discrepancy............ 10 1 10 .25 3
New Administrator Request...... 3,016 1 3,016 .08 242
Query Credit Purchase.......... 789 1 789 .08 64
Educational Request............ 10 1 10 .08 1
Account Balance Transfer....... 10 1 10 .08 1
--------------------------------------------------------------------------------
Total...................... 6,059,761 .............. 6,059,761 ............... 326,120
----------------------------------------------------------------------------------------------------------------
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.
Amy McNulty,
Acting Director, Division of the Executive Secretariat.
[FR Doc. 2017-19252 Filed 9-11-17; 8:45 am]
BILLING CODE 4165-15-P
