Federal Register / Vol. 71, No.
148 / Wednesday, August 2, 2006 / Notices
1992 (57 FR 48801); February 28, 1994
(59 FR 9486); April 29, 1996 (61 FR
18744; November 17, 1997 (62 FR
61332); October 21, 1999 (64 FR 56792);
October 25, 2001 (66 FR 54014) and
November 7, 2003 (68 FR 63098).
Notice of the availability of drafts of
these six updated and one new
toxicological profiles for public review
and comment will be published in the
Federal Register on/or about October
17, 2006, with notice of a 90-day public
comment period for each profile,
starting from the actual release date.
Following the close of the comment
period, chemical-specific comments
will be addressed, and, where
appropriate, changes will be
incorporated into each profile.
Development of Toxicological Profiles
This notice announces the
development of one new and six
updated toxicological profiles of priority
hazardous substances comprising the
twentieth set prepared by ATSDR.
The following toxicological profiles
are now being developed:
SET 20 TOXICOLOGICAL PROFILES
Toxicological profile
1. Aluminum ..........................
2. Cresols .............................
3. Diazinon ............................
4. Dichloropropene, 1,3 ........
5. Guthion* ............................
6. Phenol ..............................
7. Tetrachloroethane,
1,1,2,2- ..............................
* Denotes new profile.
Dated: July 28, 2006.
Ken Rose,
Acting Director, Office of Policy, Planning
and Evaluation, National Center for
Environmental Health, Agency for Toxic
Substances and Disease, Disease Registry.
[FR Doc. E6–12417 Filed 8–1–06; 8:45 am]
BILLING CODE 4163–70–P
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HS grant and budget instrument .....................................................................................
Estimated total annual burden hours:
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43775
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
National Center for Environmental
Health/Agency for Toxic Substances
and Disease Registry; The Program
Peer Review Subcommittee of the
Board of Scientific Counselors (BSC),
Centers for Disease Control and
Prevention (CDC), National Center for
Environmental Health/Agency or Toxic
Substances and Disease Registry
(NCEH/ATSDR): Teleconference
In accordance with section 10(a)(2) of the
Federal Advisory Committee Act (Pub. L. 92–
463), CDC, NCEH/ATSDR announces the
following subcommittee meeting:
Name: Program Peer Review Subcommittee
(PPRS).
Time and Date: 10 a.m.–12 p.m. Eastern
Daylight Savings Time, August 14, 2006.
Place: The teleconference will originate at
NCEH/ATSDR in Atlanta, Georgia. To
participate, dial 877–315–6535 and enter
conference code 383520.
Purpose: Under the charge of the BSC,
NCEH/ATSDR, the PPRS will provide the
Board with advice and recommendations on
NCEH/ATSDR program peer review. They
will serve the function of organizing,
facilitating, and providing a long-term
CAS number perspective to the conduct of NCEH/ATSDR
program peer review.
7429–90–5 Matters to be Discussed: A review of the
1319–77–3 minutes from the previous meeting; a review
0333–41–5 and discussion of the draft Program Peer
0542–75–6 Review Self-Assssment Tool questionnaire; a
0086–50–0 review and discussion of the partners’ and
0108–95–2 senior management questionnaires; a
discussion of the peer review site visit for the
Division of Health Assessment and
0079–34–5
Consultation and the Division of Regional
Operation; and a discussion of the peer
review timeline.
Due to programmatic matters, this
Federal Register Notice is being
published on less than 15 calendar days
notice to the public (41 CFR 102–
.3.150(b))
Agenda items are subject to change as
priorities dictate.
FOR FURTHER INFORMATION CONTACT:
Sandra Malcom, Committee
Management Specialist, office of
Science, NCEH/ATSDR, M/S E–28, 1600
ANNUAL BURDEN ESTIMATES
Instrument
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Clifton Road, NE., Atlanta, Georgia
30333, telephone 404–498–0622.
SUPPLEMENTARY INFORMATION: Public
comment period is scheduled for 11:30
a.m.–11:40 a.m.
The Director, Management Analysis
and Services Office, has been delegated
the authority to sign Federal Register
notices pertaining to announcements of
meetings and other committee
management activities for both CDC and
NCEH/ATSDR. Analysis and Services
Office, Centers for Disease Control and
Prevention.
Dated: July 28, 2006.
Alvin Hall,
Director, Management Analysis and Services
Office, Centers for Disease Control and
Prevention.
[FR Doc. 06–6665 Filed 8–1–06; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
[OMB No.: 0970–0207]
Submission for OMB Review;
Comment Request; Head Start
Program Grant Application and Budget
Instrument
Description: The Head Start Bureau is
proposing to renew, without changes,
the Head Start Grant Application and
Budget Instrument, which standardizes
the grant application information that is
requested from all Head Start and Early
Head Start grantees applying for
continuation grants. The application
and budget forms are available on a data
diskette and on the web at
www.acfgabi.com. Completed
applications can be transmitted
electronically to Regional and Central
Offices. The Administration on
Children, Youth and Families believes
that this application document makes
the process of applying for Head Start
program grants more efficient for
applicants.
Respondents: Head Start and Early
Head Start grantees.
Number of Average
Number of responses burden Total bur-
respondents per re- hours per den hours
spondent response
1,600 1 33 52,800
.................... .................... .................... 52,800
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 43776 Federal Register / Vol. 71, No. 148 / Wednesday, August 2, 2006 / Notices
Additional Information: Copies of the
proposed collection may be obtained 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.
OMB Comment: OMB is required to
make a decision concerning the
collection information between 30 and
60 days after publication of this
document in the Federal Register.
Therefore, a comment is best assured of
having its full effect if OMB receives it
within 30 days of publication. Written
comments and recommendations for the
proposed information collection should
be sent directly to the following:
Office of Management and Budget,
Paperwork Reduction Project, 725
17th Street, NW., Washington, DC
20503, Attn: Desk Officer for ACF, E-
mail address:
Katherine_T._Astrich@eop.gov.
P&A SGP .........................................................................................................................
Estimated Total Annual Burden Hours:
Additional Information: Copies of the
proposed collection may be obtained 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. All requests
should be identified by the title of the
information collection: E-mail address:
infocollection@acf.hhs.gov.
OMB Comment: OMB is required to
make a decision concerning the
collection of information between 30
and 60 days after publication of this
document in the Federal Register.
Therefore, a comment is best assured of
having its full effect if OMB receives it
within 30 days of publication. Written
comments and recommendations for the
proposed information collection should
be sent directly to the following:
Office of Management and Budget,
Paperwork Reduction Project, 725
wwhite on PROD1PC61 with NOTICES
17th Street, NW., Washington, DC
20503, Attn: Desk Officer for ACF, E-
mail address: KetherinelT.l
Astrich@omb.eop.gov.
VerDate Aug<31>2005 16:40 Aug 01, 2006
Dated: July 27, 2006. coming fiscal year. While the P&A is
Robert Sargis, mandated to protect and advocate under
Reports Clearance Officer. a range of different Federally authorized
[FR Doc. 06–6619 Filed 8–1–06; 8:45 am] disabilities programs, only the PADD
BILLING CODE 4184–01–M program requires an SGP. Following the
required public input for the coming
fiscal year, the P&As submit the final
DEPARTMENT OF HEALTH AND version of this SGP to the
HUMAN SERVICES Administration on Developmental
Disabilities (ADD). ADD will aggregate
Administration for Children and the information in the SGPs into a
Families national profile of programmatic
[OMB No. 0980–0270] emphasis for P&A Systems in the
coming year. This aggregation will
Submission for OMB Review; provide ADD with a tool for monitoring
Comment Request; Developmental of the public input requirement.
Disabilities Protection and Advocacy Furthermore, it will provide an
Statement of Goals and Priorities overview of program direction, and
Description: Federal statute and permit ADD to track accomplishments
regulation require each State Protection against goals/targets, permitting the
and Advocacy (P&A) System to prepare formulation of technical assistance and
and submit to public comment a compliance with the Government
Statement of Goals and Priorities (SGP) Performance and Results Act of 1993.
for the P&A for Developmental Respondents: State and Tribal
Disabilities (PADD) program for each Governments.
ANNUAL BURDEN ESTIMATES
Number of Average
Number of responses burden Total bur-
Instrument respondents per re- hours per den hours
spondent response
57 1 44 2,508
2,508
Dated: July 27, 2007. made, and on certain sponsors of such
Robert Sargis, animal drug applications and/or
Reports Clearance Officer. investigational animal drug
[FR Doc. 06–6620 Filed 8–1–06; 8:45 am] submissions. This notice establishes the
BILLING CODE 4184–01–M
fee rates for FY 2007.
For FY 2007, the animal drug user fee
rates are: $168,600 for an animal drug
DEPARTMENT OF HEALTH AND application; $84,300 for a supplemental
HUMAN SERVICES animal drug application for which
safety or effectiveness data is required;
Food and Drug Administration $4,115 for an annual product fee;
$51,350 for an annual establishment fee;
Animal Drug User Fee Rates and and $44,850 for an annual sponsor fee.
Payment Procedures for Fiscal Year FDA will issue invoices for FY 2007
2007 product, establishment, and sponsor
fees by December 30, 2006, and these
AGENCY: Food and Drug Administration,
invoices will be due and payable by
HHS.
January 31, 2007.
ACTION: Notice.
The application fee rates are effective
for applications submitted on or after
SUMMARY: The Food and Drug
Administration (FDA) is announcing the October 1, 2006, and will remain in
rates and payment procedures for fiscal effect through September 30, 2007.
year (FY) 2007 animal drug user fees. Applications will not be accepted to
The Federal Food, Drug, and Cosmetic review until FDA has received full
Act (the act), as amended by the Animal payment of application fees and any
Drug User Fee Act of 2003 (ADUFA), other animal drug user fees owed.
authorizes FDA to collect user fees for FOR FURTHER INFORMATION CONTACT: Visit
certain animal drug applications, on the FDA Web site at http://www.fda.gov/
certain animal drug products, on certain oc/adufa or contact Robert Miller,
establishments where such products are Center for Veterinary Medicine (HFV–
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