Agency Forms Undergoing Paperwork Reduction Act Review, 28882-28883 [2012-11871]
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28882
Federal Register / Vol. 77, No. 95 / Wednesday, May 16, 2012 / Notices
groups with approximately 75
providers.
Information collected through followup surveys of patients and providers
will be used to assess changes in
knowledge, attitudes, beliefs and
behavior regarding cervical cancer
screening. Qualitative information
collected during the focus groups with
providers will be used to identify
facilitators and barriers to acceptance
and appropriate use of the HPV test and
longer screening intervals. Findings
from the CX3 study will help inform
NBCCEDP standards for primary
cervical cancer screening, including
reimbursement guidelines for the HPV
DNA test.
Participation in the CX3 study is
voluntary and there are no costs to
respondents other than their time. OMB
approval is requested for one year.
Because the majority of information
collection activities were completed in
the first three years of the study, the
estimated burden to respondents will
decrease in the final year of OMB
approval. The total estimated
annualized burden hours are 135.
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Type of respondent
Form name
Patients ...................................................
Providers .................................................
Follow-up Patient Survey .......................................
Follow-up Provider Survey .....................................
Focus Group Moderator Guide ..............................
Kimberly S. Lane,
Deputy Director, Office of Science Integrity,
Office of the Associate Director for Science,
Office of the Director, Centers for Disease
Control and Prevention.
Health (NIOSH), Centers for Disease
Control and Prevention (CDC).
[FR Doc. 2012–11874 Filed 5–15–12; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–12–0566]
Agency Forms Undergoing Paperwork
Reduction Act Review
The Centers for Disease Control and
Prevention (CDC) publishes a list of
information collection requests under
review by the Office of Management and
Budget (OMB) in compliance with the
Paperwork Reduction Act (44 U.S.C.
Chapter 35). To request a copy of these
requests, call the CDC at (404) 639–7570
or send an email to omb@cdc.gov. Send
written comments to CDC Desk Officer,
Office of Management and Budget,
Washington, DC 20503 or by fax to (202)
395–5806. Written comments should be
received within 30 days of this notice.
Proposed Project
srobinson on DSK4SPTVN1PROD with NOTICES
Evaluation of Worker Notification
Program (0920–0566, Expiration 2/28/
2011)—Reinstatement—National
Institute for Occupational Safety and
Background and Brief Description
The National Institute for
Occupational Safety and Health
(NIOSH), under Section 20(a)(1), (a)(4),
(a)(7)(c), and Section 22(d), (e)(5)(7) of
the Occupational Safety and Health Act
(29 U.S.C. 669), ‘‘has the responsibility
to conduct research relating to
occupational safety and health relating
to innovative methods, techniques, and
approaches for dealing with
occupational safety and health
problems.’’ Although the research
studies continued, the notification
activities were discontinued after the
extension ICR was not submitted to
OMB before the original expiration date.
Since the Right to Know movement in
the late 1970s, NIOSH has been
developing methods and materials to
notify subjects of its epidemiological
studies. Within NIOSH, notifying
workers of past exposures is done to
inform surviving cohort members of
findings from NIOSH studies. Current
NIOSH policy dictates how and when
worker notification should occur. The
extent of the notification effort depends
upon the level of excess mortality or the
extent of the disease or illness found in
the study population. Current
notification efforts range from posting
results at the facilities studied to
mailing individual letters to surviving
members of the study population and
other stakeholders. Each year, the
Number of
responses
per
respondent
150
70
75
Average
burden per
response
(in hours)
1
1
1
10/60
30/60
1
NIOSH Industrywide Studies Branch
(IWSB), Division of Surveillance,
Hazard Evaluation, and Field Studies
(DSHEFS) typically prepares materials
for two to three completed studies. This
often requires individual letters be
mailed to study populations ranging in
size from 200–20,000 workers each. An
evaluation instrument would gauge the
effectiveness of notification materials
and improve future communication of
risk information.
The purpose of the proposed Reader
Response Postcard is to obtain feedback
from workers that would improve the
quality and usefulness of the Institute’s
worker notification activities. The actual
number of notifications required in a
given year cannot be known in advance.
Each year, the NIOSH IWSB, DSHEFS,
typically prepares materials for two to
three completed studies. This often
requires individual letters be mailed to
study populations ranging in size from
200–20,000 workers each, averaging
8,000/yr. Researchers from NIOSH
propose to routinely include a Reader
Response postcard with notification
materials to assess the value and
usefulness of said materials. The Reader
Response postcard was tested internally
and the average time to complete was 10
minutes. We are requesting approval for
three years. Participation is voluntary
and there is no cost to respondents
except for their time. The total
estimated annual burden hours are
1,333.
ESTIMATED ANNUALIZED BURDEN HOURS
Form name
Number of
respondents
Number of
responses
Avg. burden
per response
(hours)
Reader Response Card ...............................................................................................................
8,000
1
10/60
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Federal Register / Vol. 77, No. 95 / Wednesday, May 16, 2012 / Notices
Kimberly S. Lane,
Deputy Director, Office of Scientific Integrity,
Office of the Associate Director for Science,
Office of the Director, Centers for Disease
Control and Prevention.
[FR Doc. 2012–11871 Filed 5–15–12; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[Docket No. CDC–2012–0004]
Draft Public Health Action Plan—A
National Public Health Action Plan for
the Detection, Prevention, and
Management of Infertility
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
ACTION: Notice of availability and
request for public comment.
AGENCY:
The Centers for Disease
Control and Prevention (CDC), located
within the Department of Health and
Human Services (HHS) is publishing
this notice requesting public comment
on the draft National Public Health
Action Plan for the Detection,
Prevention, and Management of
Infertility. The draft plan can be found
at https://www.regulations.gov Docket
No. CDC–2012–0004. Also found in the
docket is a supporting document for
reference, the Outline for a National
Action Plan for the Prevention,
Detection, and Management of
Infertility, which was subsequently
developed into the present Plan.
DATES: Written comments must be
received on or before June 15, 2012.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2012–
0004, by any of the following methods:
• Internet: Access the Federal
eRulemaking portal at https://
www.regulations.gov. Follow the
instructions for submitting comments.
• Mail: Centers for Disease Control
and Prevention, National Center for
Chronic Disease Prevention and Health
Promotion, Division of Reproductive
Health, Attn: National Public Health
Action Plan for the Detection,
Prevention, and Management of
Infertility, Docket No. CDC–2012–0004,
4770 Buford Highway NE., Mailstop K–
34, Atlanta, Georgia, 30341.
Instructions: All submissions received
must include the agency name and
docket number for this notice. All
relevant comments received will be
posted publicly without change,
including any personal or proprietary
srobinson on DSK4SPTVN1PROD with NOTICES
SUMMARY:
VerDate Mar<15>2010
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Jkt 226001
information provided. To download an
electronic version of the plan, access
https://www.regulations.gov. Written
comments, identified by Docket No.
CDC–2012–0004, will be available for
public inspection Monday through
Friday, except for legal holidays, from 9
a.m. until 5 p.m., Eastern Daylight Time,
at 2900 Woodcock Blvd., Atlanta,
Georgia 30341. Please call ahead to
(770) 488–5200 and ask for a
representative from the Division of
Reproductive Health to schedule your
visit. Comments may also be viewed at
www.regulations.gov.
FOR FURTHER INFORMATION CONTACT:
Denise Jamieson, Centers for Disease
Control and Prevention, National Center
for Chronic Disease Prevention and
Health Promotion, Division of
Reproductive Health, 4770 Buford
Highway NE., Mailstop K–34, Atlanta,
Georgia 30341, (770)488–5200.
SUPPLEMENTARY INFORMATION: In 2007, a
CDC-wide ad hoc workgroup formed to
examine the full scope of infertility
activities across the agency. This
workgroup conducted an assessment to
identify gaps and opportunities in
public health surveillance, research,
communications, programs, and policy
development, which led to the 2010
publication of a white paper outlining
the need for a national plan, with a
public health focus, on infertility
prevention, detection, and management.
In consultation with many
governmental and nongovernmental
partners, CDC developed the National
Public Health Action Plan for the
Detection, Prevention and Management
of Infertility. Addressing both male and
female infertility, the plan outlines and
summarizes actions needed to promote,
preserve, and restore the ability of
women in the United States to conceive,
carry a pregnancy to term, and deliver
a healthy infant. This goal extends
beyond simply addressing the inability
to conceive but also focuses on reducing
the burden of impaired fecundity by
promoting behaviors that maintain
fertility; by promoting prevention, early
detection, and treatment of medical
conditions; and by reducing
environmental and occupational threats
to fertility. Given the public health
focus of this action plan, promoting
healthy pregnancy outcomes associated
with treating and managing infertility is
also important, as is improving the
efficacy and safety of infertility
treatment.
The document is organized into three
chapters: ‘‘Detection of Infertility,’’
‘‘Prevention of Infertility,’’ and
‘‘Management of Infertility.’’ Each
chapter addresses the topic’s public
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28883
health importance, existing challenges,
and opportunities for action to decrease
the impact of infertility on the public’s
health. The suggested opportunities
provide federal and other government
agencies, professional and consumer
organizations, and other partners and
stakeholders a foundation and platform
to work together to decrease the burden
of infertility in the United States.
Dated: May 9, 2012.
Kathleen Sebelius,
Secretary.
[FR Doc. 2012–11774 Filed 5–15–12; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2012–N–0009]
Cooperative Agreement To Support
Innovation in Vaccine Clinical Trial
Design and Collaboration in
Pharmacovigilance To Advance Global
Access to Safe and Effective Vaccines
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
The Food and Drug
Administration (FDA) announces its
intention to accept and consider a single
source application for an award of a
cooperative agreement to the World
Health Organization (WHO) in support
of collaborative efforts to advance
innovative approaches to vaccine
clinical trial design and to enhance the
utilization of a range of
pharmacovigilance tools as a means to
further vaccine safety and potentially
facilitate more rapid introduction of
new vaccines. The goal of FDA’s Center
for Biologics Evaluation and Research
(CBER) is to enhance technical
collaboration and cooperation between
FDA, WHO, and its Member States to
facilitate strengthening regulatory
capacity globally.
DATES: Important dates are as follows:
1. The application due date is June 15,
2012.
2. The anticipated start date is
September 15, 2012.
3. The expiration date is June 16,
2012.
ADDRESSES: Submit the paper
application to: Vieda Hubbard, Grants
Management (HFA–500), 5630 Fishers
Lane, Rockville, MD 20857, and a copy
to Leslie Haynes, Center for Biologics
Evaluation and Research, Office of the
Director (HFM–30), 1401 Rockville Pike,
Rockville, MD 20852–1448. For more
SUMMARY:
E:\FR\FM\16MYN1.SGM
16MYN1
Agencies
[Federal Register Volume 77, Number 95 (Wednesday, May 16, 2012)]
[Notices]
[Pages 28882-28883]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-11871]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30Day-12-0566]
Agency Forms Undergoing Paperwork Reduction Act Review
The Centers for Disease Control and Prevention (CDC) publishes a
list of information collection requests under review by the Office of
Management and Budget (OMB) in compliance with the Paperwork Reduction
Act (44 U.S.C. Chapter 35). To request a copy of these requests, call
the CDC at (404) 639-7570 or send an email to omb@cdc.gov. Send written
comments to CDC Desk Officer, Office of Management and Budget,
Washington, DC 20503 or by fax to (202) 395-5806. Written comments
should be received within 30 days of this notice.
Proposed Project
Evaluation of Worker Notification Program (0920-0566, Expiration 2/
28/2011)--Reinstatement--National Institute for Occupational Safety and
Health (NIOSH), Centers for Disease Control and Prevention (CDC).
Background and Brief Description
The National Institute for Occupational Safety and Health (NIOSH),
under Section 20(a)(1), (a)(4), (a)(7)(c), and Section 22(d), (e)(5)(7)
of the Occupational Safety and Health Act (29 U.S.C. 669), ``has the
responsibility to conduct research relating to occupational safety and
health relating to innovative methods, techniques, and approaches for
dealing with occupational safety and health problems.'' Although the
research studies continued, the notification activities were
discontinued after the extension ICR was not submitted to OMB before
the original expiration date.
Since the Right to Know movement in the late 1970s, NIOSH has been
developing methods and materials to notify subjects of its
epidemiological studies. Within NIOSH, notifying workers of past
exposures is done to inform surviving cohort members of findings from
NIOSH studies. Current NIOSH policy dictates how and when worker
notification should occur. The extent of the notification effort
depends upon the level of excess mortality or the extent of the disease
or illness found in the study population. Current notification efforts
range from posting results at the facilities studied to mailing
individual letters to surviving members of the study population and
other stakeholders. Each year, the NIOSH Industrywide Studies Branch
(IWSB), Division of Surveillance, Hazard Evaluation, and Field Studies
(DSHEFS) typically prepares materials for two to three completed
studies. This often requires individual letters be mailed to study
populations ranging in size from 200-20,000 workers each. An evaluation
instrument would gauge the effectiveness of notification materials and
improve future communication of risk information.
The purpose of the proposed Reader Response Postcard is to obtain
feedback from workers that would improve the quality and usefulness of
the Institute's worker notification activities. The actual number of
notifications required in a given year cannot be known in advance. Each
year, the NIOSH IWSB, DSHEFS, typically prepares materials for two to
three completed studies. This often requires individual letters be
mailed to study populations ranging in size from 200-20,000 workers
each, averaging 8,000/yr. Researchers from NIOSH propose to routinely
include a Reader Response postcard with notification materials to
assess the value and usefulness of said materials. The Reader Response
postcard was tested internally and the average time to complete was 10
minutes. We are requesting approval for three years. Participation is
voluntary and there is no cost to respondents except for their time.
The total estimated annual burden hours are 1,333.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Avg. burden
Form name Number of Number of per response
respondents responses (hours)
----------------------------------------------------------------------------------------------------------------
Reader Response Card......................................... 8,000 1 10/60
----------------------------------------------------------------------------------------------------------------
[[Page 28883]]
Kimberly S. Lane,
Deputy Director, Office of Scientific Integrity, Office of the
Associate Director for Science, Office of the Director, Centers for
Disease Control and Prevention.
[FR Doc. 2012-11871 Filed 5-15-12; 8:45 am]
BILLING CODE 4163-18-P