Submission for OMB Review; Comment Request; A Generic Submission for Formative Research, Pre-Testing, Stakeholder Measures and Advocate Forms at NCI, 28994-28995 [2011-12375]
Download as PDF
<![CDATA[
28994
Federal Register / Vol. 76, No. 97 / Thursday, May 19, 2011 / Notices
use of the system, personnel security,
contingency planning, technical
controls, information sharing, and
public access controls.
4. Review CICP Request for Benefits
System Controls: Perform an
independent review or audit of the CICP
Request for Benefits system security
control in accordance with applicable
Federal requirements and/or guidelines.
5. Authorize Processing: Ensure that a
management official authorizes, in
writing, confirmation that the security
plan as implemented adequately secures
the CICP Request for Benefits system.
The CICP Request for Benefits system
must be authorized prior to operating
and reauthorized in accordance with
applicable Federal requirements and/or
guidelines.
6. Implementation Guidelines: DHHS
Chapter 45–13 ‘‘Safeguarding Records
Contained in Systems of Records;’’ the
Information Security Program Policy,
HHS IRM Policy 2004–002.001 (Dec. 15,
2004); and Appendix III to OMB
Circular No. A–130 ‘‘Security of Federal
Automated Information Resources;’’
Appendix I to OMB Circular No. A–130,
‘‘Federal Agency Responsibilities for
Maintaining Records About
Individuals.’’
RETENTION AND DISPOSAL:
HRSA is working with NARA to
obtain the appropriate retention value.
Records will be retained and disposed
of in accordance with the Records
Control Schedule of the Health
Resources and Services Administration.
SYSTEM MANAGER(S) AND ADDRESS:
Director, Countermeasures Injury
Compensation Program, Healthcare
Systems Bureau, Health Resources and
Services Administration, 5600 Fishers
Lane, Room 11C–06, Rockville,
Maryland 20857, or the Director’s
designee.
pertaining to another individual under
false pretenses is a criminal offense
under the Privacy Act subject to a
$5,000 fine (45 CFR 5b.5(b)(2)(ii)).
Requests in person: Record access
procedures are the same as notification
procedures. The requester should
provide a reasonable description of the
contents of the record being sought.
Records will be mailed only to the
requester’s address that is on file, unless
a different address is demonstrated by
official documentation. A parent or
guardian who requests notification of, or
access to, a minor/legally incompetent
person’s medical records must verify
his/her relationship to the minor/legally
incompetent person as well as his/her
own identity and shall designate a
family physician or other health
professional (other than a family
member) to whom the record, if any,
will be sent.
Requests by telephone/facsimile/
electronic mail: Since positive
identification of the requester cannot be
established, telephone, facsimile, or
electronic mail (e-mail) requests will not
be honored.
RECORD ACCESS PROCEDURES:
Record access procedures are the
same as Requests in Person procedures
above.
CONTESTING RECORDS PROCEDURES:
To contest a record in the system,
contact the System Manager at the
address specified above and reasonably
identify the record, stipulate the
information being contested, state the
corrective action sought and the
reason(s) for requesting the correction,
along with supporting documentation to
show how the record is inaccurate,
incomplete, untimely, or irrelevant.
jlentini on DSK4TPTVN1PROD with NOTICES
NOTIFICATION PROCEDURE:
RECORD SOURCE CATEGORIES:
Requests must be made to the System
Manager.
Requests by mail: Requests for
information and/or access to records
received by mail must contain
information providing the identity of
the writer, and a reasonable description
of the record desired, and whom it
concerns. Written requests must contain
the name and address of the requester,
his/her date of birth and his/her
signature for comparison purposes.
Requests must be notarized to verify the
identity of the requester, or the
requester must certify that (s)he is the
individual who (s)he claims to be and
that (s)he understands that to knowingly
and willfully request or acquire a record
Sources of records include, but are
not limited to, countermeasure
recipients and/or their legal or personal
representatives under the
Countermeasures Injury Compensation
Program, and any other sources of
information or documentation
submitted by any other person or entity
for inclusion in a request for the
purpose of determining medical or legal
eligibility for, or amount of benefits
and/or compensation under, the
Program (e.g., Federal, State, or local
government or private health care
entities participating in the
administration of covered
countermeasures under a Secretarial
declaration).
VerDate Mar<15>2010
15:54 May 18, 2011
Jkt 223001
PO 00000
Frm 00047
Fmt 4703
Sfmt 4703
SYSTEMS EXEMPTED FROM CERTAIN PROVISIONS
OF THE ACT:
None.
[FR Doc. 2011–12258 Filed 5–18–11; 8:45 am]
BILLING CODE 4160–15–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Submission for OMB Review;
Comment Request; A Generic
Submission for Formative Research,
Pre-Testing, Stakeholder Measures
and Advocate Forms at NCI
Summary: Under the provisions of
Section 3507(a)(1)(D) of the Paperwork
Reduction Act of 1995, the National
Cancer Institute (NCI), 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. This proposed information
collection was previously published in
the Federal Register on March 15, 2011
(76 FR 14034) 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. The 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.
Proposed Collection: Title: A Generic
Submission for Formative Research, Pretesting, Stakeholder Measures and
Advocate Forms at NCI. Type of
Information Collection Request: New.
Need and Use of Information Collection:
In order to carry out NCI’s legislative
mandate, the Office of Advocacy
Relations (OAR) disseminates cancerrelated information to a variety of
stakeholders, seeks their input and
feedback, and facilitates collaboration
between the Institute and these external
partners to advance NCI’s authorized
programs. It is beneficial for NCI,
through the OAR, to pretest strategies,
concepts, activities and materials while
they are under development.
Additionally, administrative forms may
be part of this generic submission since
they are a necessary part of collecting
demographic information and areas of
interest for advocates. Pre-testing, or
formative evaluation, helps ensure that
the products and services developed by
NCI have the greatest capacity of being
received, understood, and accepted by
their target audiences. Since OAR is
E:\FR\FM\19MYN1.SGM
19MYN1
28995
Federal Register / Vol. 76, No. 97 / Thursday, May 19, 2011 / Notices
responsible for matching advocates to
NCI programs and initiatives across the
cancer continuum, it necessary to
measure the satisfaction of both internal
and external stakeholders with this
collaboration. This customer satisfaction
research helps ensure the relevance,
utility, and appropriateness of the many
initiatives and products that OAR and
NCI produce. The OAR will use a
variety of qualitative (focus groups,
interviews) and quantitative (paper,
phone, in-person, and web surveys)
methodologies to conduct this research,
allowing NCI to: (1) Understand
characteristics (attitudes, beliefs, and
behaviors) of the intended target
audience and use this information in the
development of effective strategies,
concepts, activities; (2) use a feedback
loop to help refine, revise, and enhance
OAR’s efforts—ensuring that they have
the greatest relevance, utility,
appropriateness, and impact for/to
target audiences; and (3) expend limited
program resource dollars wisely and
effectively. Frequency of Response: On
occasion. Affected Public: Individuals or
households; Businesses or other for
profit; Not-for-profit institutions and
organizations; Federal Government;
State, Local, or Tribal Government. Type
of Respondents: Adult cancer research
advocates; members of the public;
health care professionals; organizational
representatives. Table 1 outlines the
estimated burden hours required for a
three-year approval of this generic
submission. There are no Capital Costs,
Operating Costs, and/or Maintenance
Costs to report.
TABLE 1—ESTIMATE OF BURDEN HOURS OVER THREE YEARS
[For generic submissions]
Number of
respondents
Survey/instrument
Average time
per response
(minutes/hour)
Frequency of
response
3,600
1,800
225
300
1
1
1
1
Totals ........................................................................................
jlentini on DSK4TPTVN1PROD with NOTICES
Self-Administered Post-Activity Questionnaires ..............................
Other Self-Administered Questionnaires and Forms .......................
Individual In-Depth Interviews .........................................................
Focus Group Interviews ...................................................................
5,925
............................
Request for Comments: Written
comments and/or suggestions from the
public and affected agencies are invited
on one or more of the following points:
(1) Whether the proposed collection of
information is necessary for the proper
performance of the function of the
agency, including whether the
information will have practical utility;
(2) The accuracy of the agency’s
estimate of the burden of the proposed
collection of information, including the
validity of the methodology and
assumptions used; (3) Ways to enhance
the quality, utility, and clarity of the
information to be collected; and (4)
Ways to minimize the burden of the
collection of information on those who
are to respond, including the use of
appropriate automated, electronic,
mechanical, or other technological
collection techniques or other forms of
information technology.
Direct Comments to OMB: 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
Attention: NIH Desk Officer, Office of
Management and Budget at
OIRA_submission@omb.eop.gov or by
fax to 202–395–6974. To request more
information on the proposed project,
contact Shannon Bell, Director of Office
of Advocacy Relations (OAR), NCI, NIH,
31 Center Drive, Bldg. 31, Room 10A28,
MSC 2580, Bethesda, MD 20892, call
non-toll-free number 301–451–3393 or
VerDate Mar<15>2010
15:54 May 18, 2011
Jkt 223001
e-mail your request, including your
address to: bells@mail.nih.gov.
Comments Due Date: Comments
regarding this information collection are
best assured of having their full effect if
received within 30-days of the date of
this publication.
Dated: May 13, 2011.
Vivian Horovitch-Kelley,
NCI Project Clearance Liaison, National
Institutes of Health.
[FR Doc. 2011–12375 Filed 5–18–11; 8:45 am]
BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Eunice Kennedy Shriver National
Institute of Child Health & Human
Development; Notice of Closed
Meeting
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended (5 U.S.C. App.), 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
PO 00000
Frm 00048
Fmt 4703
Sfmt 9990
20/60
60/60
60/60
90/60
Annual burden
hours
(.33)
(1.0)
(1.0)
(1.5)
1,200
1,800
225
450
............................
3,675
would constitute a clearly unwarranted
invasion of personal privacy.
Name of Committee: National Institute of
Child Health and Human Development Initial
Review Group, Health, Behavior, and Context
Subcommittee.
Date: June 20–21, 2011.
Time: 8 a.m. to 5 p.m.
Agenda: To review and evaluate grant
applications.
Place: Doubletree Hotel Bethesda,
(Formerly Holiday Inn Select), 8120
Wisconsin Avenue, Bethesda, MD 20814.
Contact Person: Michele C. HindiAlexander, PhD, Scientific Review Officer,
Division of Scientific Review, Eunice
Kennedy Shriver National Institute of Child
Health and Human Development, NIH 6100
Executive Blvd., Room 5B01, Bethesda, MD
20892, 301–435–8382,
hindialm@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)
Dated: May 13, 2011.
Jennifer S. Spaeth,
Director, Office of Federal Advisory
Committee Policy.
[FR Doc. 2011–12336 Filed 5–18–11; 8:45 am]
BILLING CODE 4140–01–P
E:\FR\FM\19MYN1.SGM
19MYN1
]]>Agencies
[Federal Register Volume 76, Number 97 (Thursday, May 19, 2011)]
[Notices]
[Pages 28994-28995]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-12375]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
Submission for OMB Review; Comment Request; A Generic Submission
for Formative Research, Pre-Testing, Stakeholder Measures and Advocate
Forms at NCI
Summary: Under the provisions of Section 3507(a)(1)(D) of the
Paperwork Reduction Act of 1995, the National Cancer Institute (NCI),
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. This proposed information
collection was previously published in the Federal Register on March
15, 2011 (76 FR 14034) 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. The 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.
Proposed Collection: Title: A Generic Submission for Formative
Research, Pre-testing, Stakeholder Measures and Advocate Forms at NCI.
Type of Information Collection Request: New. Need and Use of
Information Collection: In order to carry out NCI's legislative
mandate, the Office of Advocacy Relations (OAR) disseminates cancer-
related information to a variety of stakeholders, seeks their input and
feedback, and facilitates collaboration between the Institute and these
external partners to advance NCI's authorized programs. It is
beneficial for NCI, through the OAR, to pretest strategies, concepts,
activities and materials while they are under development.
Additionally, administrative forms may be part of this generic
submission since they are a necessary part of collecting demographic
information and areas of interest for advocates. Pre-testing, or
formative evaluation, helps ensure that the products and services
developed by NCI have the greatest capacity of being received,
understood, and accepted by their target audiences. Since OAR is
[[Page 28995]]
responsible for matching advocates to NCI programs and initiatives
across the cancer continuum, it necessary to measure the satisfaction
of both internal and external stakeholders with this collaboration.
This customer satisfaction research helps ensure the relevance,
utility, and appropriateness of the many initiatives and products that
OAR and NCI produce. The OAR will use a variety of qualitative (focus
groups, interviews) and quantitative (paper, phone, in-person, and web
surveys) methodologies to conduct this research, allowing NCI to: (1)
Understand characteristics (attitudes, beliefs, and behaviors) of the
intended target audience and use this information in the development of
effective strategies, concepts, activities; (2) use a feedback loop to
help refine, revise, and enhance OAR's efforts--ensuring that they have
the greatest relevance, utility, appropriateness, and impact for/to
target audiences; and (3) expend limited program resource dollars
wisely and effectively. Frequency of Response: On occasion. Affected
Public: Individuals or households; Businesses or other for profit; Not-
for-profit institutions and organizations; Federal Government; State,
Local, or Tribal Government. Type of Respondents: Adult cancer research
advocates; members of the public; health care professionals;
organizational representatives. Table 1 outlines the estimated burden
hours required for a three-year approval of this generic submission.
There are no Capital Costs, Operating Costs, and/or Maintenance Costs
to report.
Table 1--Estimate of Burden Hours Over Three Years
[For generic submissions]
----------------------------------------------------------------------------------------------------------------
Average time
Survey/instrument Number of Frequency of per response Annual burden
respondents response (minutes/hour) hours
----------------------------------------------------------------------------------------------------------------
Self-Administered Post-Activity 3,600 1 20/60 (.33) 1,200
Questionnaires.........................
Other Self-Administered Questionnaires 1,800 1 60/60 (1.0) 1,800
and Forms..............................
Individual In-Depth Interviews.......... 225 1 60/60 (1.0) 225
Focus Group Interviews.................. 300 1 90/60 (1.5) 450
-----------------------------------------------------------------------
Totals.............................. 5,925 ................ ................ 3,675
----------------------------------------------------------------------------------------------------------------
Request for Comments: Written comments and/or suggestions from the
public and affected agencies are invited on one or more of the
following points: (1) Whether the proposed collection of information is
necessary for the proper performance of the function of the agency,
including whether the information will have practical utility; (2) The
accuracy of the agency's estimate of the burden of the proposed
collection of information, including the validity of the methodology
and assumptions used; (3) Ways to enhance the quality, utility, and
clarity of the information to be collected; and (4) Ways to minimize
the burden of the collection of information on those who are to
respond, including the use of appropriate automated, electronic,
mechanical, or other technological collection techniques or other forms
of information technology.
Direct Comments to OMB: 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 Attention: NIH Desk Officer, Office of Management and
Budget at OIRA_submission@omb.eop.gov or by fax to 202-395-6974. To
request more information on the proposed project, contact Shannon Bell,
Director of Office of Advocacy Relations (OAR), NCI, NIH, 31 Center
Drive, Bldg. 31, Room 10A28, MSC 2580, Bethesda, MD 20892, call non-
toll-free number 301-451-3393 or e-mail your request, including your
address to: bells@mail.nih.gov.
Comments Due Date: Comments regarding this information collection
are best assured of having their full effect if received within 30-days
of the date of this publication.
Dated: May 13, 2011.
Vivian Horovitch-Kelley,
NCI Project Clearance Liaison, National Institutes of Health.
[FR Doc. 2011-12375 Filed 5-18-11; 8:45 am]
BILLING CODE 4140-01-P
