Agency Forms Undergoing Paperwork Reduction Act Review, 6803-6804 [2012-2961]
Download as PDF
<![CDATA[
6803
Federal Register / Vol. 77, No. 27 / Thursday, February 9, 2012 / Notices
Background and Brief Description
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–0920–11CE]
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
requirement of Section 3506(c)(2)(A) of
the Paperwork Reduction Act of 1995.
To request a copy of these requests, call
the CDC Reports Clearance Officer at
(404) 639–5960 or send an email to
omb@cdc.gov. Send written comments
to CDC Desk Officer, Office of
Management and Budget, Washington,
DC or by fax to (202) 395–6974. Written
comments should be received within 30
days of this notice.
Proposed Project
The National Health and Nutrition
Examination Survey (NHANES) 1999–
2010 Birth Certificate Linkage Study—
Pregnant Women—New—National
Center for Health Statistics (NCHS),
Centers for Disease Control and
Prevention (CDC).
Section 306 of the Public Health
Service (PHS) Act (42 U.S.C. 242k), as
amended, authorizes that the Secretary
of Health and Human Services (DHHS),
acting through NCHS, shall collect
statistics on the extent and nature of
illness and disability; environmental,
social and other health hazards; and
determinants of health of the population
of the United States.
Division of Health and Nutrition
Examination Surveys (DHANES)
proposes to re-contact women who were
pregnant at the time of their
participation in NHANES in 1999–2010
and ask permission to link their data to
the child’s birth certificate data, for the
birth that resulted after the survey. This
study is funded in collaboration with
CDC’s National Center for Chronic
Disease Prevention and Health
Promotion, Division of Reproductive
Health (DRH). Participation is
completely voluntary and confidential.
NHANES was conducted periodically
between 1970 and 1994, and
continuously since 1999 by the NCHS.
A supplemental sample of pregnant
women was selected in NHANES from
1999–2006. This resulted in a total of
1,350 pregnant women. Although this
supplemental sample was discontinued
after 2006, there are an estimated 150
pregnant women in the NHANES
sample for the years 2007–10. This
results in a total estimate of 1,500
women for this project.
The NHANES only collected
information about the pregnant women
at the time of interview. Having
information on their children’s birth
certificates and birth outcomes could
provide insight into issues related to
maternal and child health. No other
survey has the physical examination
and nutritional data that NHANES
collects on pregnant women.
Consents for these projects will be
sent to the appropriate U.S. states, local
areas, or territories, where the birth
certificate retrievals will then be
conducted. Electronic retrieval per
records is estimated at five minutes.
NHANES data users include the U.S.
Congress; the World Health
Organization; numerous Federal
agencies such as the National Institutes
of Health, the Environmental Protection
Agency, and the United States
Department of Agriculture; private
groups such as the American Heart
Association; schools of public health;
private businesses; individual
practitioners; and administrators. This
submission requests approval for two
years. There is no cost to respondents
other than their time. The total
estimated annual burden is 312 hours.
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Number of
responses per
respondent
Average
burden per
response
(in hours)
Type of respondent
Form
Women who were pregnant during
NHANES 1999–2010.
3. State/local vital statistics staff (one per
U.S. State or Territory).
Health Questionnaire/Consent Form .............
750
1
20/60
Locate and transmit birth certificates .............
57
13
5/60
1.
Kimberly S. Lane,
Acting Reports Clearance Officer, Centers for
Disease Control and Prevention.
[FR Doc. 2012–2965 Filed 2–8–12; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–12–11JZ]
mstockstill on DSK4VPTVN1PROD with NOTICES
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
VerDate Mar<15>2010
19:21 Feb 08, 2012
Jkt 226001
PO 00000
Frm 00032
Fmt 4703
Sfmt 4703
requests, call the CDC Reports Clearance
Officer 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
Underreporting of Occupational
Injuries and Illnesses by Workers—
New—National Institute for
Occupational Safety and Health
(NIOSH), Centers for Disease Control
and Prevention (CDC).
E:\FR\FM\09FEN1.SGM
09FEN1
6804
Federal Register / Vol. 77, No. 27 / Thursday, February 9, 2012 / Notices
Background and Brief Description
In 2008, the Congressional Committee
on Education and Labor released the
report, ‘‘Hidden Tragedy:
Underreporting of Workplace Injuries
and Illnesses,’’ indicating ‘‘that workrelated injuries and illnesses in the
United States are chronically and even
grossly underreported.’’ Based in part
on the report’s results, Congress
allocated funds for NIOSH to conduct a
follow-up study using NIOSH’s
occupational supplement to the
National Electronic Injury Surveillance
System (NEISS–Work) to estimate
underreporting among individuals who
seek care at an emergency department
(ED) for an occupational illness, injury,
or exposure.
Objectives for this project are to (1)
assess the reporting behavior of workers
that are injured, ill, or exposed to a
harmful substance at work; (2)
characterize the chronic aspects of
work-related injuries or illnesses; and
(3) estimate the prevalence of workrelated chronic injuries and illnesses
among United States workers treated in
EDs. Particular attention will be paid to
self-employed workers, workers with
work-related illnesses, and workers with
chronic health problems.
Data collection for the telephone
interview survey will be done via a
questionnaire containing questions
about the respondent’s injury, illness, or
exposure that sent them to the ED; the
characteristics of the job they were
working when they were injured,
became ill, or were exposed; their
experiences reporting their injury,
illness, or exposure to the ED and their
employer (if applicable); the presence of
an underlying chronic condition that
was associated with their ED visit; and
the nature of any other work-related
chronic conditions they have
experienced. The questionnaire was
designed to take 30 minutes to complete
and includes a brief series of questions
to screen out individuals who were not
seen in the ED for a work-related injury,
illness, or exposure; who are younger
than age 20 or older than age 64; who
do not speak English or Spanish; or who
were working as volunteers or day
laborers when the injury, illness, or
exposure occurred or was made worse.
Approximately 1,500 to 3,000
interviews will be completed over the
two year period. The only cost to the
respondent will be the cost of their time
spent on the phone completing the
telephone interview survey. The total
estimated burden hours are 750.
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Respondents
U.S. workers presenting to an emergency department ..............................................................
Kimberly S. Lane,
Reports Clearance Officer, Centers for Disease
Control and Prevention.
[FR Doc. 2012–2961 Filed 2–8–12; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2012–N–0001]
Advisory Committee for Reproductive
Health Drugs; Notice of Meeting
AGENCY:
Food and Drug Administration,
HHS.
mstockstill on DSK4VPTVN1PROD with NOTICES
ACTION:
Notice.
This notice announces a forthcoming
meeting of a public advisory committee
of the Food and Drug Administration
(FDA). The meeting will be open to the
public.
Name of Committee: Advisory
Committee for Reproductive Health
Drugs.
General Function of the Committee:
To provide advice and
recommendations to the Agency on
FDA’s regulatory issues.
Date and Time: The meeting will be
held on April 5, 2012, from 8 a.m. to
4:30 p.m.
Location: FDA White Oak Campus,
Building 31, the Great Room, White Oak
VerDate Mar<15>2010
18:04 Feb 08, 2012
Jkt 226001
Conference Center (rm. 1503), 10903
New Hampshire Ave., Silver Spring, MD
20993–0002. Information regarding
special accommodations due to a
disability, visitor parking and
transportation may be accessed at
https://www.fda.gov/Advisory
Committees/default.htm; under the
heading ‘‘Resources for You’’, click on
‘‘Public Meetings at the FDA White Oak
Campus.’’ Please note that visitors to the
White Oak Campus must enter through
Building 1.
Contact Person: Kalyani Bhatt, Center
for Drug Evaluation and Research, Food
and Drug Administration, 10903 New
Hampshire Ave., WO31–2417, Silver
Spring, MD 20993–0002, 301–796–9001,
Fax: 301–847–8533, email:
ACRHD@fda.hhs.gov, or FDA Advisory
Committee Information Line, 1–800–
741–8138 (301–443–0572 in the
Washington, DC area), and follow the
prompts to the desired center or product
area. Please call the Information Line for
up-to-date information on this meeting.
A notice in the Federal Register about
last minute modifications that impact a
previously announced advisory
committee meeting cannot always be
published quickly enough to provide
timely notice. Therefore, you should
always check the Agency’s Web site and
call the appropriate advisory committee
hot line/phone line to learn about
PO 00000
Frm 00033
Fmt 4703
Sfmt 4703
1,500
Number of
responses
per
respondent
Average
burden per
response
(in hours)
1
30/60
possible modifications before coming to
the meeting.
Agenda: The committee will discuss
the benefits and risks of mirabegron
(YM178), under new drug application
(NDA) 202611, submitted by Astellas
Pharma Global Development Inc., for
the proposed indication of treatment of
overactive bladder (OAB) with
symptoms of urge urinary incontinence,
urgency, and urinary frequency.
Mirabegron is a beta-3-adrenoceptor
(AR) agonist and is a new molecular
entity. The benefit/risk discussion will
focus on the adequacy of the
demonstration of efficacy and safety in
the treatment of OAB.
FDA intends to make background
material available to the public no later
than two business days before the
meeting. If FDA is unable to post the
background material on its Web site
prior to the meeting, the background
material will be made publicly available
at the location of the advisory
committee meeting, and the background
material will be posted on FDA’s Web
site after the meeting. Background
material is available at https://www.fda.
gov/AdvisoryCommittees/Calendar/
default.htm. Scroll down to the
appropriate advisory committee link.
Procedure: Interested persons may
present data, information, or views,
orally or in writing, on issues pending
before the committee. Written
E:\FR\FM\09FEN1.SGM
09FEN1
]]>Agencies
[Federal Register Volume 77, Number 27 (Thursday, February 9, 2012)]
[Notices]
[Pages 6803-6804]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-2961]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30Day-12-11JZ]
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 Reports Clearance Officer 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
Underreporting of Occupational Injuries and Illnesses by Workers--
New--National Institute for Occupational Safety and Health (NIOSH),
Centers for Disease Control and Prevention (CDC).
[[Page 6804]]
Background and Brief Description
In 2008, the Congressional Committee on Education and Labor
released the report, ``Hidden Tragedy: Underreporting of Workplace
Injuries and Illnesses,'' indicating ``that work-related injuries and
illnesses in the United States are chronically and even grossly
underreported.'' Based in part on the report's results, Congress
allocated funds for NIOSH to conduct a follow-up study using NIOSH's
occupational supplement to the National Electronic Injury Surveillance
System (NEISS-Work) to estimate underreporting among individuals who
seek care at an emergency department (ED) for an occupational illness,
injury, or exposure.
Objectives for this project are to (1) assess the reporting
behavior of workers that are injured, ill, or exposed to a harmful
substance at work; (2) characterize the chronic aspects of work-related
injuries or illnesses; and (3) estimate the prevalence of work-related
chronic injuries and illnesses among United States workers treated in
EDs. Particular attention will be paid to self-employed workers,
workers with work-related illnesses, and workers with chronic health
problems.
Data collection for the telephone interview survey will be done via
a questionnaire containing questions about the respondent's injury,
illness, or exposure that sent them to the ED; the characteristics of
the job they were working when they were injured, became ill, or were
exposed; their experiences reporting their injury, illness, or exposure
to the ED and their employer (if applicable); the presence of an
underlying chronic condition that was associated with their ED visit;
and the nature of any other work-related chronic conditions they have
experienced. The questionnaire was designed to take 30 minutes to
complete and includes a brief series of questions to screen out
individuals who were not seen in the ED for a work-related injury,
illness, or exposure; who are younger than age 20 or older than age 64;
who do not speak English or Spanish; or who were working as volunteers
or day laborers when the injury, illness, or exposure occurred or was
made worse.
Approximately 1,500 to 3,000 interviews will be completed over the
two year period. The only cost to the respondent will be the cost of
their time spent on the phone completing the telephone interview
survey. The total estimated burden hours are 750.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Average
Number of Number of burden per
Respondents respondents responses per response (in
respondent hours)
----------------------------------------------------------------------------------------------------------------
U.S. workers presenting to an emergency department.............. 1,500 1 30/60
----------------------------------------------------------------------------------------------------------------
Kimberly S. Lane,
Reports Clearance Officer, Centers for Disease Control and Prevention.
[FR Doc. 2012-2961 Filed 2-8-12; 8:45 am]
BILLING CODE 4163-18-P
