Agency Forms Undergoing Paperwork Reduction Act Review, 29243-29245 [2011-12469]
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29243
Federal Register / Vol. 76, No. 98 / Friday, May 20, 2011 / Notices
Depository institutions that provide
periodic statements are required to
include information about fees imposed,
interest earned, and the annual
percentage yield earned during those
statement periods. TISA and Regulation
DD mandate the methods by which
institutions determine the account
balance on which interest is calculated.
They also contain rules about
advertising deposit accounts and
overdraft services.
Current Actions: On March 1, 2011,
the Federal Reserve published a notice
in the Federal Register (76 FR 11246)
requesting public comment for 60 days
on the extension, without revision, of
the disclosure requirements in
connection with Regulation DD. The
comment period for this notice expired
on May 2, 2011. The Federal Reserve
did not receive any comments.
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) 639–5960 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.
Board of Governors of the Federal Reserve
System, May 17, 2011.
Jennifer J. Johnson,
Secretary of the Board.
Background
[FR Doc. 2011–12418 Filed 5–19–11; 8:45 am]
BILLING CODE 6210–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day-11–0138]
Agency Forms Undergoing Paperwork
Reduction Act Review
The Centers for Disease Control and
Prevention (CDC) publishes a list of
Proposed Project
Pulmonary Function Testing Course
Approval Program, 29 CFR 1910.1043—
Extension—(OMB No.0920–0138, Exp
8/31/2011). The National Institute for
Occupational Safety and Health
(NIOSH), Centers for Disease Control
and Prevention (CDC).
NIOSH has the responsibility under
the Occupational Safety and Health
Administration’s Cotton Dust Standard,
29 CFR 1920.1043, for approving
courses to train technicians to perform
pulmonary function testing in the cotton
industry. Successful completion of a
NIOSH-approved course is mandatory
under the Standard. To carry out its
responsibility, NIOSH maintains a
Pulmonary Function Testing Course
Approval Program. The program
consists of an application submitted by
potential sponsors (universities,
hospitals, and private consulting firms)
who seek NIOSH approval to conduct
courses, and if approved, notification to
NIOSH of any course or faculty changes
during the approval period, which is
limited to five years. The application
form and added materials, including an
agenda, curriculum vitae, and course
materials are reviewed by NIOSH to
determine if the applicant has
developed a program which adheres to
the criteria required in the Standard.
Following approval, any subsequent
changes to the course are submitted by
course sponsors via letter or e-mail and
reviewed by NIOSH staff to assure that
the changes in faculty or course content
continue to meet course requirements.
Course sponsors also voluntarily submit
an annual report to inform NIOSH of
their class activity level and any faculty
changes. Sponsors who elect to have
their approval renewed for an additional
5 year period submit a renewal
application and supporting
documentation for review by NIOSH
staff to ensure the course curriculum
meets all current standard requirements.
Approved courses that elect to offer
NIOSH–Approved Spirometry Refresher
Courses must submit a separate
application and supporting documents
for review by NIOSH staff. Institutions
and organizations throughout the
country voluntarily submit applications
and materials to become course sponsor
and carry out training. Submissions are
required for NIOSH to evaluate a course
and determine whether it meets the
criteria in the Standard and whether
technicians will be adequately trained
as mandated under the Standard. There
are no costs to the respondents other
than their time. The estimated annual
burden to respondents is 196 hours.
Number of
respondents
Forms for respondents
Initial Application ..........................................................................................................................
Annual Report ..............................................................................................................................
Report for Course Changes ........................................................................................................
Renewal Application ....................................................................................................................
Refresher Course Application ......................................................................................................
Dated: May 13, 2011.
Daniel Holcomb,
Reports Clearance Officer, Centers for Disease
Control and Prevention.
[FR Doc. 2011–12470 Filed 5–19–11; 8:45 am]
jlentini on DSK4TPTVN1PROD with NOTICES
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–11–11BF]
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
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3
35
12
13
10
Average
burden/
response
(in hrs)
Number of
responses/
respondent
1
1
1
1
1
3.5
30/60
45/60
6.0
8.0
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) 639–5960 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) 395–5806. Written
comments should be received within 30
days of this notice.
E:\FR\FM\20MYN1.SGM
20MYN1
29244
Federal Register / Vol. 76, No. 98 / Friday, May 20, 2011 / Notices
Proposed Project
Contact Investigation Outcome
Reporting Forms—New—National
Center for Emerging, Zoonotic and
Infectious Diseases (NCEZID), Centers
for Disease Control and Prevention
(CDC).
Background and Brief Description
CDC proposes to collect passengerlevel, epidemiologic, demographic, and
health status data from state/local
Health Departments and maritime
operators at the conclusion of contact
investigations of individuals believed to
have been exposed to a communicable
disease during travel. The information
requested by CDC would be obtained by
the health departments or maritime
operators while conducting the contact
investigation according to their
established policies and procedures,
and would be reported to CDC on a
voluntary basis. This information will
assist CDC in fulfilling its regulatory
responsibility to prevent the
importation of communicable diseases
from foreign countries (42 CFR part 71)
and interstate control of communicable
diseases in humans (42 CFR part 70). To
perform these tasks in a streamlined
manner and ensure that all relevant
information is collected in the most
efficient and timely manner possible,
Quarantine Stations use a number of
forms: Contact Investigation Outcome
Reporting Forms: (1) Optional TB Air/
Land Contact Investigation Outcome
Reporting, (2) Optional Measles,
Mumps, or Rubella Air/Land Contact
Investigation Outcome Reporting, (3)
Optional General Air/Land Contact
Investigation Outcome Reporting Form,
(4) Optional TB Maritime Contact
Investigation Outcome Reporting Form,
(5) Optional Measles, Mumps or Rubella
Maritime Contact Investigation Outcome
Reporting Form, (6) Optional General
Maritime Contact Investigation Outcome
Reporting Form.
Section 361 of the Public Health
Service (PHS) Act (42 U.S.C. 264)
authorizes the Secretary of Health and
Human Services to make and enforce
regulations necessary to prevent the
introduction, transmission or spread of
communicable diseases from foreign
countries into the United States. The
regulations that implement this law, 42
CFR Parts 70 and 71, require
conveyances to report an ‘‘ill person’’ or
any death onboard to authorized
quarantine officers and other personnel
to inspect and undertake necessary
control measures with respect to
conveyances (e.g., airplanes, cruise
ships), persons, and shipments of
animals and etiologic agents in order to
protect the public health. The
notification is made possible by
contacting individuals who may have
been exposed to a communicable
disease during travel and their contacts,
and investigating this exposure so that
the necessary medical or public health
interventions can be implemented.
CDC provides state and local health
departments and maritime conveyance
operators with information to notify and
contact individuals and further
investigate this exposure by contacting
others who may have been potentially
exposed to disease. However, there
currently is no standardized tool or form
to collect pertinent information
regarding the outcome of such
investigations.
To address the need to inform CDC of
additional actions that may be needed to
further protect public health based on
the outcome of the contact
investigations, CDC has developed six
forms to assist health departments and
maritime conveyance operators in
reporting back to CDC. The forms are
specific to the nature of the
investigation; Tuberculosis (TB),
Measles, Mumps, and Rubella or the
General forms specific to other diseases
of public health concern. The purpose
of the forms is the same: to collect
information to help CDC quarantine
officials to fully understand the extent
of disease spread and transmission
during travel and to inform the
development and or refinement of
investigative protocols, aimed at
reducing the spread of communicable
disease.
All six forms collect the following
categories of information: Heath status
of traveler, clinical history including
diagnosis, and interventions related to
exposure.
Respondents are state and local health
departments and maritime conveyance
operators. Respondents will use these
standardized forms to submit data to
CDC for each individual contacted via a
secure means of their choice, e.g., webbased application, fax or e-mail.
The estimated total burden on the
public, included in the chart below, can
vary a great deal depending on the
number of flights and the number of
individuals identified as contacts that
are assigned to a given health
jurisdiction in the U.S. There is no cost
to respondents other than their time.
The total estimated annual burden
hours are 280.
ESTIMATE ANNUALIZED BURDEN HOURS
Number of
respondents
Respondents
jlentini on DSK4TPTVN1PROD with NOTICES
State/Local health department staff .............................................................................................
State/Local health department staff .............................................................................................
State/Local health department staff .............................................................................................
Maritime Operators ......................................................................................................................
Maritime Operators ......................................................................................................................
Maritime Operators ......................................................................................................................
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E:\FR\FM\20MYN1.SGM
2154
367
456
190
140
40
20MYN1
Average
burden/
response
(in hours)
Number of
responses/
respondent
1
1
1
1
1
1
5/60
5/60
5/60
5/60
5/60
5/60
Federal Register / Vol. 76, No. 98 / Friday, May 20, 2011 / Notices
Dated: May 13, 2011.
Daniel Holcomb,
Acting Reports Clearance Officer, Centers for
Disease Control and Prevention.
[FR Doc. 2011–12469 Filed 5–19–11; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–11–11CB]
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) 639–5960 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) 395–5806. Written
comments should be received within 30
days of this notice.
Proposed Project
SEARCH for Diabetes in Youth
Study—New—Division of Diabetes
Translation, National Center for Chronic
Disease Prevention and Health
Promotion (NCCDPHP), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
Diabetes is one of the most common
chronic diseases among children in the
United States. When diabetes strikes
during childhood, it is routinely
assumed to be type 1, or juvenile-onset,
diabetes. Type 1 diabetes (T1D)
develops when the body’s immune
system destroys pancreatic cells that
make the hormone insulin. Type 2
diabetes begins when the body develops
a resistance to insulin and no longer
uses it properly. As the need for insulin
rises, the pancreas gradually loses its
ability to produce sufficient amounts of
insulin to regulate blood sugar.
Reports of increasing frequency of
both type 1 and type 2 diabetes in youth
have been among the most concerning
aspects of the evolving diabetes
epidemic. In response to this growing
public health concern, the Centers for
Disease Control and Prevention (CDC)
and the National Institutes of Health
(NIH) funded the SEARCH for Diabetes
in Youth Study.
The SEARCH for Diabetes in Youth
Study began in 2000 as a multi-center,
epidemiological study, conducted in six
geographically dispersed Study Centers
that reflected the racial and ethnic
diversity of the U.S. Phases 1 (2000–
2005) and 2 (2005–2010) produced
estimates of the prevalence and
incidence of diabetes among youth age
< 20 years, according to diabetes type,
age, sex, and race/ethnicity, and
characterized selected acute and chronic
complications of diabetes and their risk
factors, as well as the quality of life and
quality of health care.
CDC proposes to collect de-identified,
case-level information from five
SEARCH sites during Phase 3 of the
SEARCH for Diabetes in Youth Study.
Phase 3 brings together major and
timely facets of childhood diabetes
research: An epidemiologic component
that assesses temporal trends in the
incidence of diabetes in youth; a
pathophysiologic component addressing
the natural history of diabetes in youth;
a health services research component to
evaluate the processes and quality of
care for youth with diabetes; and a
public health perspective on case
classification of diabetes in youth.
Information will be collected for three
years through a data collection
29245
contractor, which will serve as the
SEARCH Study Coordinating Center.
Data will be transmitted electronically
to the Coordinating Center through a
secure, dedicated Web site. Information
can be entered and transmitted at any
time. The information collection has
three components.
The Registry Study will collect
information on newly diagnosed
incident diabetes cases in youth age
< 20 years. CDC estimates that each
clinical site will identify and register an
average of 255 cases per year. The items
collected for each case include an
inpatient survey, core information,
medications, and physical exam data.
The total estimated annualized burden
for this information collection is 744
hours.
The Cohort Study is a longitudinal
research study about SEARCH cases
whose diabetes was incident in 2002 or
later. CDC estimates that each clinical
site will conduct follow-up on an
average of 142 cases per year. The items
collected for each case include health
questionnaires for youth and parents,
physical exam information, and surveys
about eating behavior, blood sugar,
neuropathy, family relationships, and
quality of life. Information will also be
collected to monitor unanticipated
occurrences and conditions. CDC
estimates that each site will report an
average of 13 unanticipated occurrences
per year.
Respondents will be the five study
sites funded for SEARCH Phase 3.
Participation in the data collection is
required for the study sites, but
participation in the SEARCH study is
voluntary for individuals who are
followed at those sites.
The total estimated annualized
burden is 2,132 hours. There are no
costs to respondents other than their
time.
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
responses per
respondent
Number of
respondents
Type of respondents
jlentini on DSK4TPTVN1PROD with NOTICES
SEARCH Clinical Sites: Registry Study .........
5
255
SEARCH Clinical Sites: Cohort Study ............
5
142
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Form name
Extended Core ...............................................
Medication Inventory ......................................
Inpatient Survey .............................................
Specimen Collection (Registry) ......................
Physical Exam (Registry) ...............................
Health Questionnaire-Youth ...........................
Health Questionnaire-Parent ..........................
CES–Depression ............................................
Medical Record Validation .............................
Quality of Care ...............................................
Peds QL .........................................................
SEARCH MNSI Neuropathy ..........................
Diabetes Eating Survey .................................
E:\FR\FM\20MYN1.SGM
20MYN1
Average
burden per
response
10/60
5/60
10/60
5/60
5/60
15/60
15/60
4/60
10/60
13/60
5/60
5/60
5/60
]]>Agencies
[Federal Register Volume 76, Number 98 (Friday, May 20, 2011)]
[Notices]
[Pages 29243-29245]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-12469]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30Day-11-11BF]
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) 639-5960 or send an e-mail
to omb@cdc.gov. Send written comments to CDC Desk Officer, Office of
Management and Budget, Washington, DC or by fax to (202) 395-5806.
Written comments should be received within 30 days of this notice.
[[Page 29244]]
Proposed Project
Contact Investigation Outcome Reporting Forms--New--National Center
for Emerging, Zoonotic and Infectious Diseases (NCEZID), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
CDC proposes to collect passenger-level, epidemiologic,
demographic, and health status data from state/local Health Departments
and maritime operators at the conclusion of contact investigations of
individuals believed to have been exposed to a communicable disease
during travel. The information requested by CDC would be obtained by
the health departments or maritime operators while conducting the
contact investigation according to their established policies and
procedures, and would be reported to CDC on a voluntary basis. This
information will assist CDC in fulfilling its regulatory responsibility
to prevent the importation of communicable diseases from foreign
countries (42 CFR part 71) and interstate control of communicable
diseases in humans (42 CFR part 70). To perform these tasks in a
streamlined manner and ensure that all relevant information is
collected in the most efficient and timely manner possible, Quarantine
Stations use a number of forms: Contact Investigation Outcome Reporting
Forms: (1) Optional TB Air/Land Contact Investigation Outcome
Reporting, (2) Optional Measles, Mumps, or Rubella Air/Land Contact
Investigation Outcome Reporting, (3) Optional General Air/Land Contact
Investigation Outcome Reporting Form, (4) Optional TB Maritime Contact
Investigation Outcome Reporting Form, (5) Optional Measles, Mumps or
Rubella Maritime Contact Investigation Outcome Reporting Form, (6)
Optional General Maritime Contact Investigation Outcome Reporting Form.
Section 361 of the Public Health Service (PHS) Act (42 U.S.C. 264)
authorizes the Secretary of Health and Human Services to make and
enforce regulations necessary to prevent the introduction, transmission
or spread of communicable diseases from foreign countries into the
United States. The regulations that implement this law, 42 CFR Parts 70
and 71, require conveyances to report an ``ill person'' or any death
onboard to authorized quarantine officers and other personnel to
inspect and undertake necessary control measures with respect to
conveyances (e.g., airplanes, cruise ships), persons, and shipments of
animals and etiologic agents in order to protect the public health. The
notification is made possible by contacting individuals who may have
been exposed to a communicable disease during travel and their
contacts, and investigating this exposure so that the necessary medical
or public health interventions can be implemented.
CDC provides state and local health departments and maritime
conveyance operators with information to notify and contact individuals
and further investigate this exposure by contacting others who may have
been potentially exposed to disease. However, there currently is no
standardized tool or form to collect pertinent information regarding
the outcome of such investigations.
To address the need to inform CDC of additional actions that may be
needed to further protect public health based on the outcome of the
contact investigations, CDC has developed six forms to assist health
departments and maritime conveyance operators in reporting back to CDC.
The forms are specific to the nature of the investigation; Tuberculosis
(TB), Measles, Mumps, and Rubella or the General forms specific to
other diseases of public health concern. The purpose of the forms is
the same: to collect information to help CDC quarantine officials to
fully understand the extent of disease spread and transmission during
travel and to inform the development and or refinement of investigative
protocols, aimed at reducing the spread of communicable disease.
All six forms collect the following categories of information:
Heath status of traveler, clinical history including diagnosis, and
interventions related to exposure.
Respondents are state and local health departments and maritime
conveyance operators. Respondents will use these standardized forms to
submit data to CDC for each individual contacted via a secure means of
their choice, e.g., web-based application, fax or e-mail.
The estimated total burden on the public, included in the chart
below, can vary a great deal depending on the number of flights and the
number of individuals identified as contacts that are assigned to a
given health jurisdiction in the U.S. There is no cost to respondents
other than their time. The total estimated annual burden hours are 280.
Estimate Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Average
Number of Number of burden/
Respondents respondents responses/ response (in
respondent hours)
----------------------------------------------------------------------------------------------------------------
State/Local health department staff............................. 2154 1 5/60
State/Local health department staff............................. 367 1 5/60
State/Local health department staff............................. 456 1 5/60
Maritime Operators.............................................. 190 1 5/60
Maritime Operators.............................................. 140 1 5/60
Maritime Operators.............................................. 40 1 5/60
----------------------------------------------------------------------------------------------------------------
[[Page 29245]]
Dated: May 13, 2011.
Daniel Holcomb,
Acting Reports Clearance Officer, Centers for Disease Control and
Prevention.
[FR Doc. 2011-12469 Filed 5-19-11; 8:45 am]
BILLING CODE 4163-18-P
