Proposed Information Collection Activity; Comment Request, 11027-11028 [07-1144]
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Federal Register / Vol. 72, No. 47 / Monday, March 12, 2007 / Notices
consistently the leading cause of lost
work days in the industry. The objective
of this project is to develop a selfadministered, paper and pencil risk
assessment tool for the development of
low back disorders specifically directed
towards use in the mining industry.
Many current methods of assessing the
risk of low back disorders do not
address stressors that are relatively
unique to the mining environment,
including the restricted vertical spaces
to assess the degree of risk for the job
and the individual. The tool will be
useful in both prioritizing jobs that need
interventions to reduce low back
disorder risk, and in evaluating the
effectiveness of interventions through
tool administration before and after the
implementation of an intervention.
There will be no cost to respondents
other than their time. The total
estimated annualized burden hours are
80.
in many coal mines that require workers
to adopt stooping or kneeling postures
for extended periods of their workday.
The low back exposure assessment
tool for mining will assess various
occupational exposures associated with
development of back disorders in the
literature (postural demands, lifting,
whole body vibration exposure,
individual and psychosocial issues), as
well as specific mining stressors and
will develop a score that will be used
ESTIMATED ANNUALIZED BURDEN HOURS
Respondents
Number of
respondents
Number of
responses per
respondent
Average
burden per
response
(in hours)
Surface and Underground Miners ...............................................................................................
320 miners
1
15/60
Dated: March 5, 2007.
Joan F. Karr,
Acting Reports Clearance Officer, Centers for
Disease Control and Prevention.
[FR Doc. E7–4368 Filed 3–9–07; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Proposed Information Collection
Activity; Comment Request
Proposed Projects
Title: Tribal Child Support
Enforcement Direct Funding Request
and Reports
OMB No. 0970–0218
Description: The final rule within 45
CFR part 309, published in the Federal
Register on March 30, 2004, contains a
regulatory reporting requirement that in
order to receive funding for a Tribal IV–
D program a Tribal or Tribal
organization must submit a plan
describing how the Tribe or Tribal
organization meets or plans to meet the
objectives of section 455(f) of the Social
Security Act, including establishing
paternity, establishing, modifying, and
enforcing support orders, and locating
noncustodial parents. The plan is
required for all Tribes requesting
funding; however, once a Tribe has met
the requirements to operate a
comprehensive program, a new plan is
not required annually unless a Tribe
makes changes to its title IV–D program.
Tribes and Tribal organizations must
respond if they wish to operate a fully
funded program. In addition, any Tribe
or Tribal organization participating in
the program will be required to submit
form OCSE 34A. This paperwork
collection activity is set to expire in
April 2007.
Respondents: Tribes and Tribal
Organizations.
ANNUAL BURDEN ESTIMATES
Number of
respondents
Instrument
45 CFR 309—Plan ..........................................................................................
Form OCSE 34A ..............................................................................................
pwalker on PROD1PC71 with NOTICES
Estimated Total Annual Burden
Hours: 17,408.
In compliance with the requirements
of Section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995, the
Administration for Children and
Families is soliciting public comment
on the specific aspects of the
information collection described above.
Copies of the proposed collection of
information can be obtained and
comments may be forwarded by writing
to the Administration for Children and
Families, Office of Administration,
VerDate Aug<31>2005
18:04 Mar 09, 2007
Jkt 211001
33
49
Office of Information Services, 370
L’Enfant Promenade, SW., Washington,
DC 20447, Attn: ACF Reports Clearance
Officer. E-mail address:
infocollection@acf.hhs.gov. All requests
should be identified by the title of the
information collection.
The Department specifically requests
comments on: (a) Whether the proposed
collection of information is necessary
for the proper performance of the
functions of the agency, including
whether the information shall have
practical utility; (b) the accuracy of the
PO 00000
Frm 00057
Fmt 4703
Sfmt 4703
Number of
responses per
respondent
1
4
Average burden hours
per response
480
8
Total burden
hours
15,840
1,568
agency’s estimate of the burden of the
proposed collection of information; (c)
the quality, utility, and clarity of the
information to be collected; and (d)
ways to minimize the burden of the
collection of information on
respondents, including through the use
of automated collection techniques or
other forms of information technology.
Consideration will be given to
comments and suggestions submitted
within 60 days of this publication.
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12MRN1
11028
Federal Register / Vol. 72, No. 47 / Monday, March 12, 2007 / Notices
Dated: March 6, 2007.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 07–1144 Filed 3–9–07; 8:45 am]
BILLING CODE 4184–01–M
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
Immune Globulins for Primary Immune
Deficiency Diseases: Antibody
Specificity, Potency and Testing;
Public Workshop
AGENCY:
Food and Drug Administration,
HHS.
pwalker on PROD1PC71 with NOTICES
ACTION:
Notice of public workshop.
The Food and Drug Administration
(FDA) is announcing a public workshop
entitled: Immune Globulins for Primary
Immune Deficiency Diseases: Antibody
Specificity, Potency and Testing. The
purpose of the public workshop is to
discuss approaches to identify the most
relevant antibody specificities in
Immune Globulins for the prevention of
infections in patients with primary
immune deficiency diseases (PIDD), and
current and potential potency tests for
Immune Globulins. The public
workshop will also include a discussion
about the declining measles antibody
levels in U.S. licensed Immune
Globulins and the potential clinical
impact on patients with PIDD. The
public workshop sponsors are FDA, the
Immune Deficiency Foundation, and the
Plasma Protein Therapeutics
Association.
Date and Time: The public workshop
will be held on April 25, 2007, from 8
a.m. to 5 p.m., and April 26, 2007, from
8:30 a.m. to 11:30 a.m.
Location: The public workshop will
be held at the Lister Hill Center
Auditorium, Building 38A, National
Institutes of Health, 8800 Rockville
Pike, Bethesda, MD 20894.
Contact Person: Rhonda Dawson,
Center for Biologics Evaluation and
Research (HFM–302), Food and Drug
Administration, 1401 Rockville Pike,
suite 200N, Rockville, MD 20852–1448,
301–827–6129, FAX: 301–827–2843, email: rhonda.dawson@fda.hhs.gov.
Registration: Mail or fax your
registration information (including
name, title, firm name, address,
telephone and fax numbers) to the
contact person by April 6, 2007. There
is no registration fee for the public
workshop. Early registration is
recommended because seating is
limited. Registration on the day of the
public workshop will be provided on a
VerDate Aug<31>2005
18:04 Mar 09, 2007
Jkt 211001
space available basis beginning at 7:30
a.m.
If you need special accommodations
due to a disability, please contact
Rhonda Dawson at least 7 days in
advance of the workshop.
SUPPLEMENTARY INFORMATION: The
public workshop will feature
presentations by national and
international experts from government,
academic institutions, and industry. The
first day of the workshop will include
discussions on: (1) Epidemiology of
serious infections in PIDD patients; (2)
review of European and U.S. PIDD
registry data; (3) surveillance questions
to address the type, rate, and severity of
infections in PIDD patients; (4) rationale
for current potency tests for Immune
Globulins; (5) antibody levels in current
Immune Globulins, including those
levels to emerging pathogens; and (6)
the development of additional or other
useful potency tests. The second day of
the workshop will focus on the potential
clinical impact on PIDD patients of
declining measles antibody levels in
U.S. licensed Immune Globulins.
Transcripts: Transcripts of the public
workshop may be requested in writing
from the Freedom of Information Office
(HFI–35), Food and Drug
Administration, 5600 Fishers Lane, rm.
6–30, Rockville, MD 20857,
approximately 15 working days after the
public workshop at a cost of 10 cents
per page. A transcript of the public
workshop will be available on the
Internet at https://www.fda.gov/cber/
minutes/workshop-min.htm.
Dated: March 5, 2007.
Jeffrey Shuren,
Assistant Commissioner for Policy.
[FR Doc. E7–4313 Filed 3–9–07; 8:45 am]
BILLING CODE 4160–01–S
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Health Resources and Services
Administration
Agency Information Collection
Activities: Proposed Collection:
Comment Request
In compliance with the requirement
for opportunity for public comment on
proposed data collection projects
(section 3506(c)(2)(A) of Title 44, United
States Code, as amended by the
Paperwork Reduction Act of 1995,
Public Law 104–13), the Health
Resources and Services Administration
(HRSA) publishes periodic summaries
of proposed projects being developed
for submission to Office of Management
and Budget (OMB) under the Paperwork
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Frm 00058
Fmt 4703
Sfmt 4703
Reduction Act of 1995. To request more
information on the proposed project or
to obtain a copy of the data collection
plans and draft instruments, call the
HRSA Reports Clearance Officer on
(301) 443–1129.
Comments are invited on: (a) Whether
the proposed collection of information
is necessary for the proper performance
of the functions of the agency, including
whether the information shall have
practical utility; (b) the accuracy of the
agency’s estimate of the burden of the
proposed collection of information; (c)
ways to enhance the quality, utility, and
clarity of the information to be
collected; and (d) ways to minimize the
burden of the collection of information
on respondents, including through the
use of automated collection techniques
or other forms of information
technology.
Proposed Project: Healthcare Integrity
and Protection Data Bank for Final
Adverse Information on Health Care
Providers, Suppliers, and Practitioners
(OMB No. 0915–0239)—Extension
Section 221 (a) of the Health
Insurance Portability and
Accountability Act (HIPAA) of 1996
specifically directs the Secretary to
establish a national health care fraud
and abuse data collection program for
the reporting and disclosure of certain
final adverse actions taken against
health care providers, suppliers, and
practitioners. A final rule was published
October 26, 1999, in the Federal
Register to implement the statutory
requirements of section 1128E of the
Social Security Act (The Act) as added
by section 221 (a) of HIPAA. The Act
requires the Secretary to implement the
national health care fraud and abuse
data collection program. This data bank
is known as the Healthcare Integrity and
Protection Data Bank (HIPDB). It
contains the following types of
information: (1) Civil judgments against
a health care provider, supplier, or
practitioner in Federal or State court
related to the delivery of a health care
item or service; (2) Federal or State
criminal convictions against a health
care provider, supplier, or practitioner
related to the delivery of a health care
item or service; (3) actions by Federal or
State agencies responsible for the
licensing and certification of health care
providers, suppliers, or practitioners; (4)
exclusion of a health care provider,
practitioner or supplier from
participation in Federal or State health
care programs; and (5) any other
adjudicated actions or decisions that the
Secretary shall establish by regulations.
Access to this data bank is limited to
E:\FR\FM\12MRN1.SGM
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]]>Agencies
[Federal Register Volume 72, Number 47 (Monday, March 12, 2007)]
[Notices]
[Pages 11027-11028]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 07-1144]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families
Proposed Information Collection Activity; Comment Request
Proposed Projects
Title: Tribal Child Support Enforcement Direct Funding Request and
Reports
OMB No. 0970-0218
Description: The final rule within 45 CFR part 309, published in
the Federal Register on March 30, 2004, contains a regulatory reporting
requirement that in order to receive funding for a Tribal IV-D program
a Tribal or Tribal organization must submit a plan describing how the
Tribe or Tribal organization meets or plans to meet the objectives of
section 455(f) of the Social Security Act, including establishing
paternity, establishing, modifying, and enforcing support orders, and
locating noncustodial parents. The plan is required for all Tribes
requesting funding; however, once a Tribe has met the requirements to
operate a comprehensive program, a new plan is not required annually
unless a Tribe makes changes to its title IV-D program. Tribes and
Tribal organizations must respond if they wish to operate a fully
funded program. In addition, any Tribe or Tribal organization
participating in the program will be required to submit form OCSE 34A.
This paperwork collection activity is set to expire in April 2007.
Respondents: Tribes and Tribal Organizations.
Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Instrument Number of responses per hours per Total burden
respondents respondent response hours
----------------------------------------------------------------------------------------------------------------
45 CFR 309--Plan................................ 33 1 480 15,840
Form OCSE 34A................................... 49 4 8 1,568
----------------------------------------------------------------------------------------------------------------
Estimated Total Annual Burden Hours: 17,408.
In compliance with the requirements of Section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995, the Administration for Children and
Families is soliciting public comment on the specific aspects of the
information collection described above. Copies of the proposed
collection of information can be obtained and comments may be forwarded
by writing to the Administration for Children and Families, Office of
Administration, Office of Information Services, 370 L'Enfant Promenade,
SW., Washington, DC 20447, Attn: ACF Reports Clearance Officer. E-mail
address: infocollection@acf.hhs.gov. All requests should be identified
by the title of the information collection.
The Department specifically requests comments on: (a) Whether the
proposed collection of information is necessary for the proper
performance of the functions of the agency, including whether the
information shall have practical utility; (b) the accuracy of the
agency's estimate of the burden of the proposed collection of
information; (c) the quality, utility, and clarity of the information
to be collected; and (d) ways to minimize the burden of the collection
of information on respondents, including through the use of automated
collection techniques or other forms of information technology.
Consideration will be given to comments and suggestions submitted
within 60 days of this publication.
[[Page 11028]]
Dated: March 6, 2007.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 07-1144 Filed 3-9-07; 8:45 am]
BILLING CODE 4184-01-M
