30-day FRN

31603

Federal Register / Vol. 84, No. 127 / Tuesday, July 2, 2019 / Notices
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 Information
Collection Request must be received no
later than September 3, 2019.
ADDRESSES: Submit your comments to
[email protected] or mail the HRSA
Information Collection Clearance
Officer, Room 14N136B, 5600 Fishers
Lane, Rockville, Maryland 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 [email protected]
or call Lisa Wright-Solomon, 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:
Hospital Campaign for Organ Donation
Scorecard OMB No. 0915–0373,
Revision.
Abstract: HRSA’s Hospital Campaign
for Organ Donation enlists healthcare
organizations nationwide to increase the
number of registered organ, eye, and
tissue donors by hosting education and
donor registration events in their
facilities and communities. A scorecard

identifies activities that participants can
implement and assigns points to each
activity. Participants that earn a certain
number of points annually are
recognized by HRSA and the campaign’s
national partners.
For this information collection
request, the proposed change to the
Scorecard is the addition of the 2020
date. HRSA also intends to create a new
electronic version of the Scorecard for
future campaigns that will ultimately
reduce the level of burden for
participants. The electronic version will
be designed to be user friendly, will take
less time to complete, and will provide
HRSA with data throughout the
campaign rather than once a year.
Another benefit of an electronic
scorecard is that it will eliminate the
possibility of human error as
information will no longer be manually
entered into a database.
Need and Proposed Use of the
Information: There is a substantial
imbalance in the U.S. between the
number of people whose lives depends
on organ transplants (currently more
than 113,000) and the annual number of
organ donors (approximately 14,000
living and deceased donors). This
imbalance results in about 7,300 waiting
list deaths annually. In response to the
need for increased donation, HRSA
conducts public outreach initiatives to
encourage the American public to enroll
on state donor registries as future organ
donors.
The Scorecard motivates and
facilitates healthcare organizations’

participation in the campaign, provides
the basis for rewarding participants for
their accomplishments, and enables
HRSA to measure and evaluate
campaign process and outcome. The
scorecard also enables HRSA to make
data-based decisions and improvements
for subsequent campaigns.
Likely Respondents: The likely
respondents include the following:
Hospital development and public
relations staff of organ procurement and
other donation organizations; hospital
staff such as nurses or public relations/
communications professionals and staff
members; staff at physician’s offices,
health clinics, and emergency medical
services; or volunteers that work with
healthcare organizations on organ
donation initiatives.
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
respondents

khammond on DSKBBV9HB2PROD with NOTICES

Form name

Number of
responses per
respondent

Average
burden per
response
(in hours)

Total
responses

Total burden
hours

Activity Scorecard (online) ...................................................

1,400

1

1,400

.25

350

Total ..............................................................................

1,400

........................

1,400

........................

350

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

Maria G. Button,
Director, Division of the Executive Secretariat.

National Institutes of Health

[FR Doc. 2019–14078 Filed 7–1–19; 8:45 am]

Submission for OMB Review; 30-Day
Comment Request Scientific
Information Reporting System (SIRS)
(National Institute of General Medical
Sciences)

BILLING CODE 4165–15–P

AGENCY:

National Institutes of Health,

HHS.
ACTION:

Notice.

In compliance with the
Paperwork Reduction Act of 1995, the

SUMMARY:

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31604

Federal Register / Vol. 84, No. 127 / Tuesday, July 2, 2019 / Notices

National Institutes of Health (NIH) has
submitted to the Office of Management
and Budget (OMB) a request for review
and approval of the information
collection listed below.
DATES: Comments regarding this
information collection are best assured
of having their full effect if received by
August 1, 2019.
ADDRESSES: Written comments and/or
suggestions regarding the item(s)
contained in this notice, especially
regarding the estimated public burden
and associated response time, should be
directed to the: Office of Management
and Budget, Office of Regulatory Affairs,
[email protected] or by
fax to 202–395–6974, Attention: Desk
Officer for NIH.
FOR FURTHER INFORMATION CONTACT: To
request more information on the
proposed project or to obtain a copy of
the data collection plans and
instruments, contact: Dr. Ming Lei,
Director, Division for Research Capacity
Building, NIGMS, NIH, Natcher
Building, Room 2AS44C, 9000 Rockville
Pike, Bethesda, MD 20892, or call nontoll-free number (301) 827–5323 or
Email your request, including your
address to: [email protected].
SUPPLEMENTARY INFORMATION: This
proposed information collection was
previously published in the Federal
Register on April 4, 2019, pages 13306–
13307 (84 FR 13306) and allowed 60
days for public comment. No public
comments were received. The purpose
of this notice is to allow an additional

NIGMS aimed at developing and/or
enhancing the biomedical research
competitiveness of States and
Jurisdictions that lag in NIH funding.
The NARCH Program is an interagency
initiative that provides support to
American Indian and Alaska Native (AI/
AN) tribes and organizations for
conducting research in their
communities in order to address health
disparities, and to develop a cadre of
competitive AI/AN scientists and health
professionals. The data collected by
SIRS will provide valuable information
for the following purposes: (1)
Evaluation of progress by individual
grantees towards achieving granteedesignated and program-specified goals
and objectives, (2) evaluation of the
overall program for effectiveness,
efficiency, and impact in building
biomedical research capacity and
capability, and (3) analysis of outcome
measures to determine need for
refinements and/or adjustments of
different program features including but
not limited to initiatives and eligibility
criteria. Data collected from SIRS will
be used for various regular or ad hoc
reporting requests from interested
stakeholders that include members of
Congress, state and local officials, other
federal agencies, professional societies,
media, and other parties.
OMB approval is requested for 3
years. There are no costs to respondents
other than their time. The total
estimated annualized burden hours are
841.

30 days for public comment. The
National Institute of General Medical
Sciences (NIGMS), National Institutes of
Health, may not conduct or sponsor,
and the respondent is not required to
respond to, an information collection
that has been extended, revised, or
implemented on or after October 1,
1995, unless it displays a currently valid
OMB control number.
In compliance with Section
3507(a)(1)(D) of the Paperwork
Reduction Act of 1995, the National
Institutes of Health (NIH) has submitted
to the Office of Management and Budget
(OMB) a request for review and
approval of the information collection
listed below.
Proposed Collection: Scientific
Information Reporting System (SIRS),
0925–0735–Resinstatement Without
Change—expiration date 03/31/2019,
National Institutes of General Medical
Sciences (NIGMS), National Institutes of
Health (NIH).
Need and Use of Information
Collection: The SIRS is an online data
collection system whose purpose is to
obtain supplemental information to the
annual Research Performance Progress
Report (RPPR) submitted by grantees of
the Institutional Development Award
(IDeA) Program and the Native
American Research Centers for Health
(NARCH) Program. The SIRS will
collect program-specific data not
requested in the RPPR data collection
system. The IDeA Program is a
congressionally mandated, long-term
interventional program administered by

ESTIMATED ANNUALIZED BURDEN HOURS
Form name
SIRS ..................................................
SIRS ..................................................
SIRS ..................................................
SIRS ..................................................
SIRS ..................................................
SIRS ..................................................
Total ...........................................

khammond on DSKBBV9HB2PROD with NOTICES

Number of
respondents

Type of respondent
Principal
Phase
Principal
Phase
Principal
Phase
Principal
Principal
Principal

Total annual
burden hours

COBRE

54

1

4

216

Investigators,

COBRE

34

1

4

136

Investigators,
COBRE
III.
Investigators, INBRE .........
Investigators, IDeA–CTR ..
Investigators, NARCH .......

54

1

4

216

24
11
17

1
1
1

6
4
5

144
44
85

...........................................................

194

194

........................

841

[FR Doc. 2019–14072 Filed 7–1–19; 8:45 am]
BILLING CODE 4140–01–P

I.
II.

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
National Institute of Mental Health;
Notice of Closed Meeting
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as

17:00 Jul 01, 2019

Average time
per response
(in hours)

Investigators,

Dated: June 18, 2019.
Rusinel Amarante,
Project Clearance Liaison, National Institute
of General Medical Sciences, National
Institutes of Health.

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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,

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