Agency Forms Undergoing Paperwork Reduction Act Review, 10907-10908 [2011-4330]

Download as PDF srobinson on DSKHWCL6B1PROD with NOTICES Federal Register / Vol. 76, No. 39 / Monday, February 28, 2011 / Notices 057653–85–7, 039227–28–6, 019408– 74–3, 040321–76–4). 40. Chloroethane (CAS No. 000075– 00–3). 41. Chloromethane (CAS No. 000074– 87–3). 42. Dinitrotoluene (CAS Nos. 025321– 14–6, 000121–14–2, 000606–20–2). 43. Chloroform (CAS No. 000067–66– 3). 44. Chlorpyrifos (CAS No. 002921– 88–2). 45. Endrin (CAS Nos. 000072–20–8, 053494–70–5, 007421–93–4). 46. Tetrachloroethylene (CAS No. 000127–18–4). 47. Trichloroethylene (CAS No. 000079–01–6). 48. 1,2–Dichloroethene (CAS Nos. 000540–59–0, 000156–60–5, 000156– 59–2). 49. Carbon disulfide (CAS No. 000075–15–0). 50. 1,1–Dichloroethene (CAS No. 000075–35–4). 51. 2,4–Dinitrophenol (CAS No. 000051–28–5). 52. 4,6-Dinitro-o-cresol (CAS No. 000534–52–1). 53. Disulfoton (CAS No. 000298–04– 4). 54. Hexachlorobutadiene (CAS No. 000087–68–3). 55. Polycyclic aromatic hydrocarbons (CAS No. 130498–29–2). 56. Acetone (CAS No. 000067–64–1). 57. Chlordane (CAS Nos. 000057–74– 9, 005103–71–9, 005103–74–2, 027304– 13–8, 056641–38–4, 12789–03–6, 056534–02–2, 039765–80–5, 005103– 73–1, 003734–48–3). 58. Chlordecone/Mirex (CAS Nos. 000143–50–0, 002385–85–5). 59. Chlorinated Dibenzofurans (CDFs) (CAS Nos. 042934–53–2, 039001–02–0, 038998–75–3, 057117–31–4, 055684– 94–1, 030402–15–4, 051207–31–9, 067562–39–4, 072918–21–9, 030402– 14–3, 057117–44–9, 070648–26–9, 060851–34–5, 057117–41–6, 055673– 89–7). 60. 1,2-Dibromo-3-chloropropane (CAS Nos. 000096–12–8, 067708–83–2). 61. 1,2-Dibromoethane (CAS No. 000106–93–4). 62. 2-Hexanone (CAS No. 000591–78– 6). 63. 4,4′-Methylene bis(2chloroaniline) (CAS No. 000101–14–4). 64. N-Nitrosodiphenylamine (CAS No. 000086–30–6). 65. 2-Butanone (CAS No. 000078–93– 3). 66. 1,1-Dichloroethane (CAS No. 000075–34–3). 67. 1,2-Diphenylhydrazine (CAS No. 000122–66–7). 68. Bis(2-chloroethyl) ether (CAS No. 000111–44–4). VerDate Mar<15>2010 18:30 Feb 25, 2011 Jkt 223001 69. Chlorobenzene (CAS No. 000108– 90–7). 70. Radium (CAS Nos. 007440–14–4, 013982–63–3, 015262–20–1, 013233– 32–4). 71. Thorium (CAS Nos. 007440–29–1, 014269–63–7, 014274–82–9). 72. 1,1,2-Trichloroethane (CAS No. 000079–00–5). 73. N-Nitrosodimethylamine (CAS No. 000062–75–9). 74. N-Nitrosodi-n-propylamine (CAS No. 000621–64–7). Submission of Nominations for the Evaluation Set 25 Proposed Substances: Today’s notice invites voluntary public nominations for substances not listed in this notice. Nominations are most useful if they include the full name of the nominator, title, affiliation, e-mail address, and telephone number. ATSDR will evaluate all data and information associated with nominated substances and will determine the final list of substances to be chosen for toxicological profile development. Substances will be chosen according to ATSDR’s specific guidelines for selection. These guidelines can be found in the Selection Criteria announced in the Federal Register on May 7, 1993 (85FR27286). Please submit nominations by any of the following methods: E-mail: tpcandidatecomments@cdc.gov. Fax: 770.488.4178. Mail: CDR Jessilynn Taylor, 1600 Clifton Rd., NE., MS F–62, Atlanta, GA 30333. For further information, please contact Commander Jessilynn B. Taylor by e-mail at jxt1@cdc.gov or by phone at 770–488–3313. Please ensure that your comments are submitted within the specified nomination period. Nominations received after the closing date will be marked as late and may be considered only if time and resources permit. FOR FURTHER INFORMATION CONTACT: Ken Rose, Director, Office of Policy, Planning and Evaluation, National Center for Environmental Health/Agency for Toxic Substances and Disease Registry. [FR Doc. 2011–4327 Filed 2–25–11; 8:45 am] BILLING CODE 4163–70–P PO 00000 Frm 00034 Fmt 4703 Sfmt 4703 10907 DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention [30Day–11–0679] 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. Proposed Project Division of Heart Disease and Stroke Prevention Management Information System—Revision—National Center for Chronic Disease Prevention and Health Promotion (NCCDPHP), Centers for Disease Control and Prevention (CDC). Background and Brief Description CDC’s Division of Heart Disease and Stroke Prevention (DHDSP) is currently approved to collect progress and activity information from awardees funded through two programs: The National Heart Disease and Stroke Prevention Program (NHDSPP), and the WellIntegrated Screening and Evaluation for Women Across the Nation (WISEWOMAN) program. Information is collected semi-annually through an electronic Management Information System (MIS). The current approval is scheduled to expire 5/31/2011 (OMB No. 0920–0679). CDC requests OMB approval to continue information collection, with changes, for three years. A net reduction in the number of respondents will result in a net reduction in burden hours. Although there will be an increase in the number of awardees funded for State-based heart disease and stroke prevention (HDSP) programs, reporting requirements involving the MIS will be discontinued for awardees funded through the WISEWOMAN program. No changes are proposed to the information collection instrument, the burden per response, or the frequency of information collection. CDC currently supports populationbased heart disease and stroke prevention efforts in selected States and E:\FR\FM\28FEN1.SGM 28FEN1 10908 Federal Register / Vol. 76, No. 39 / Monday, February 28, 2011 / Notices the District of Columbia. As funding allows, CDC’s strategic plan calls for expanding the program to health departments in all U.S. States and territories. CDC works with HDSP program awardees to implement and evaluate evidence-based public health prevention and control strategies that address risk factors and reduce disparities, disease, disability, and death from heart disease and stroke. The DHDSP MIS provides a standardized, electronic interface for the collection of progress and activity information from HDSP awardees. The information collection includes work plans, objectives, partners, data sources, and policy and environmental assessments. The MIS produces both State-specific and aggregate reports that are used for performance monitoring, program evaluation, and technical assistance. The monitoring and evaluation plan for HDSP awardees is part of an overall initiative within CDC’s National Center for Chronic Disease Prevention and Health Promotion (NCCDPHP) to promote more efficient ways of using resources and achieving greater health impact. CDC will continue to use the information collected through the DHDSP MIS to identify State-specific heart disease and stroke prevention priorities and objectives, and to describe the impact and reach of program interventions. Respondents will be 42 health departments in 41 States and the District of Columbia (DC). Respondents will continue to submit their progress and activity information to CDC semiannually. There are no costs to respondents other than their time. The total estimated annualized burden hours are 504. Estimated annualized burden hours Respondents Number of respondents Number of responses per respondent Average burden per response (in hours) State-Based Heart Disease and Stroke Prevention Programs ................................................... 42 2 6 Dated: February 22, 2011. Carol Walker, Acting Reports Clearance Officer, Centers for Disease Control and Prevention. [FR Doc. 2011–4330 Filed 2–25–11; 8:45 am] BILLING CODE 4163–18–P Prevention and the Agency for Toxic Substances and Disease Registry. Dated: February 17, 2011. Elaine L. Baker, Director, Management Analysis and Services Office, Centers for Disease Control and Prevention. [FR Doc. 2011–4305 Filed 2–25–11; 8:45 am] DEPARTMENT OF HEALTH AND HUMAN SERVICES BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Disease, Disability, and Injury Prevention and Control Special Emphasis Panel (SEP): Maternal Vitamin D Status and Preterm Birth, DP11–002, Initial Review Food and Drug Administration [Docket No. FDA–2011–D–0074] Correction: The notice was published in the Federal Register on December 17, 2010, Volume 75, Number 242, Page 78999. The time and date should read as follows: srobinson on DSKHWCL6B1PROD with NOTICES Time and Date: 11 a.m.–5 p.m., April 12, 2011 (Closed). Contact Person for More Information: Donald Blackman, Ph.D., Scientific Review Officer, CDC, National Center for Chronic Disease Prevention and Health Promotion, Office of the Director, Extramural Research Program Office, 4770 Buford Highway, NE., Mailstop K– 92, Atlanta, Georgia 30341, Telephone: (770) 488–3023, E-mail: DBY7@cdc.gov. 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 the Centers for Disease Control and 18:30 Feb 25, 2011 Jkt 223001 Although you can comment on any guidance at any time (see 21 CFR 10.115(g)(5)), to ensure that the Agency considers your comment on this draft guidance before it begins work on the final version of the guidance, submit either electronic or written comments on the draft guidance by May 31, 2011. DATES: Centers for Disease Control and Prevention VerDate Mar<15>2010 administration to a patient instead of being dispensed directly to the patient for self-administration or to the patient’s caregiver for administration to the patient. Second, the draft guidance addresses when a Medication Guide will be required as part of a REMS. The draft guidance is intended to answer questions that have arisen concerning these topics. Draft Guidance for Industry on Medication Guides—Distribution Requirements and Inclusion of Medication Guides in Risk Evaluation and Mitigation Strategies; Availability AGENCY: Food and Drug Administration, HHS. ACTION: Notice. The Food and Drug Administration (FDA) is announcing the availability of a draft guidance for industry entitled ‘‘Medication Guides— Distribution Requirements and Inclusion in Risk Evaluation and Mitigation Strategies (REMS).’’ This draft guidance addresses two topics pertaining to Medication Guides for drug and biological products. First, the draft guidance addresses when FDA intends to exercise enforcement discretion regarding dispensing requirements for Medication Guides that must be distributed with a drug or biological product dispensed to a healthcare professional for SUMMARY: PO 00000 Frm 00035 Fmt 4703 Sfmt 4703 Submit written requests for single copies of the draft guidance to the Division of Drug Information, Center for Drug Evaluation and Research, Food and Drug Administration, 10903 New Hampshire Ave., Bldg. 51, rm. 2201, Silver Spring, MD 20993–0002; or the Office of Communication, Outreach and Development (HFM–40), Center for Biologics Evaluation and Research (CBER), Food and Drug Administration, 1401 Rockville Pike, Rockville, MD 20852–1448. The guidance may also be obtained by mail by calling CBER at 1– 800–835–4709 or 301–827–1800. Send one self-addressed adhesive label to assist that office in processing your requests. See the SUPPLEMENTARY INFORMATION section for electronic access to the draft guidance document. Submit electronic comments on the draft guidance to https:// www.regulations.gov. Submit written comments to the Division of Dockets Management (HFA–305), Food and Drug ADDRESSES: E:\FR\FM\28FEN1.SGM 28FEN1

Agencies

[Federal Register Volume 76, Number 39 (Monday, February 28, 2011)]
[Notices]
[Pages 10907-10908]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-4330]

-----------------------------------------------------------------------

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Centers for Disease Control and Prevention

[30Day-11-0679]

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.

Proposed Project

Division of Heart Disease and Stroke Prevention Management
Information System--Revision--National Center for Chronic Disease
Prevention and Health Promotion (NCCDPHP), Centers for Disease Control
and Prevention (CDC).

Background and Brief Description

CDC's Division of Heart Disease and Stroke Prevention (DHDSP) is
currently approved to collect progress and activity information from
awardees funded through two programs: The National Heart Disease and
Stroke Prevention Program (NHDSPP), and the Well-Integrated Screening
and Evaluation for Women Across the Nation (WISEWOMAN) program.
Information is collected semi-annually through an electronic Management
Information System (MIS). The current approval is scheduled to expire
5/31/2011 (OMB No. 0920-0679).
CDC requests OMB approval to continue information collection, with
changes, for three years. A net reduction in the number of respondents
will result in a net reduction in burden hours. Although there will be
an increase in the number of awardees funded for State-based heart
disease and stroke prevention (HDSP) programs, reporting requirements
involving the MIS will be discontinued for awardees funded through the
WISEWOMAN program. No changes are proposed to the information
collection instrument, the burden per response, or the frequency of
information collection.
CDC currently supports population-based heart disease and stroke
prevention efforts in selected States and

[[Page 10908]]

the District of Columbia. As funding allows, CDC's strategic plan calls
for expanding the program to health departments in all U.S. States and
territories. CDC works with HDSP program awardees to implement and
evaluate evidence-based public health prevention and control strategies
that address risk factors and reduce disparities, disease, disability,
and death from heart disease and stroke.
The DHDSP MIS provides a standardized, electronic interface for the
collection of progress and activity information from HDSP awardees. The
information collection includes work plans, objectives, partners, data
sources, and policy and environmental assessments. The MIS produces
both State-specific and aggregate reports that are used for performance
monitoring, program evaluation, and technical assistance. The
monitoring and evaluation plan for HDSP awardees is part of an overall
initiative within CDC's National Center for Chronic Disease Prevention
and Health Promotion (NCCDPHP) to promote more efficient ways of using
resources and achieving greater health impact.
CDC will continue to use the information collected through the
DHDSP MIS to identify State-specific heart disease and stroke
prevention priorities and objectives, and to describe the impact and
reach of program interventions. Respondents will be 42 health
departments in 41 States and the District of Columbia (DC). Respondents
will continue to submit their progress and activity information to CDC
semi-annually. There are no costs to respondents other than their time.
The total estimated annualized burden hours are 504.
Estimated annualized burden hours

----------------------------------------------------------------------------------------------------------------
Number of Average burden
Respondents Number of responses per per response
respondents respondent (in hours)
----------------------------------------------------------------------------------------------------------------
State-Based Heart Disease and Stroke Prevention Programs..... 42 2 6
----------------------------------------------------------------------------------------------------------------

Dated: February 22, 2011.
Carol Walker,
Acting Reports Clearance Officer, Centers for Disease Control and
Prevention.
[FR Doc. 2011-4330 Filed 2-25-11; 8:45 am]
BILLING CODE 4163-18-P

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