Agency Forms Undergoing Paperwork Reduction Act Review, 53311-53312 [2010-21723]

Download as PDF 53311 Federal Register / Vol. 75, No. 168 / Tuesday, August 31, 2010 / Notices Dated: August 25, 2010. Carol Walker, Acting Reports Clearance Officer, Centers for Disease Control and Prevention. [FR Doc. 2010–21737 Filed 8–30–10; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention [30-Day–10–0798] 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 Health Marketing (OMB No. 0920– 0798, exp. 01/31/2011)—Extension— Office of the Associate Director for Communication (OADC), Centers for Disease Control and Prevention (CDC). Background and Brief Description Today, CDC is globally recognized for conducting research and investigations and for its action oriented approach. CDC applies research and findings to improve people’s daily lives and responds to health emergencies— something that distinguishes CDC from its peer agencies. CDC is committed to achieving true improvements in people’s health. To do this, the agency is defining specific health protection goals to prioritize and focus its work and investments and measure progress. It is imperative that CDC provide high-quality timely information and programs in the most effective ways to help people, families, and communities protect their health and safety. Through continuous consumer feedback, prevention research, and public health information technology, we identify and evaluate health needs and interests, translate science into actions to meet those needs, and engage the public in the excitement of discovery and the progress being made to improve the health of the Nation. In our outreach to partners, we build relationships that model shared learning, mutual trust, and diversity in points of view and sectors of society. OADC is requesting a 3-year extension of OMB 0920–0798, Health Marketing, to provide feedback on the development, implementation and satisfaction regarding public health services, products, communication campaigns and information. The information will be collected using standard qualitative and quantitative methods such as interviews, focus groups, and panels, as well as questionnaires administered in person, by telephone, by mail, by e-mail, and online. More specific types of studies may include: User experience and usertesting; concept/product/package development testing; brand positioning/ identity research; customer satisfaction surveying; ethnography/observational studies; and mystery shopping. The data will be used to provide input to the development, delivery and communication of public health services and information at CDC and to address emerging programmatic needs. Every National Center and Office at CDC will have the opportunity to utilize this generic clearance. There is no cost to the respondents other than their time. The total estimated burden hours are 11,250. Type of respondents Number of respondents Number of responses per respondent Average burden per response (in hours) CDC Partners, Public Health Professionals, Health Care Professionals, General Public .......... 25,000 1 27/60 Dated: August 24, 2010. Maryam I. Daneshvar, Reports Clearance Officer, Centers for Disease Control and Prevention. [FR Doc. 2010–21736 Filed 8–30–10; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Proposed Project Centers for Disease Control and Prevention srobinson on DSKHWCL6B1PROD with NOTICES [30-Day–10–0736] 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. VerDate Mar<15>2010 16:33 Aug 30, 2010 Jkt 220001 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. Human Smoking Behavior Study— Reinstatement with Change—National Center for Chronic Disease Prevention and Health Promotion (NCCDPHP), Centers for Disease Control and Prevention (CDC). Background and Brief Description Cigarettes have been ranked as fullflavor, light or ultralight on the basis of machine-measured levels of smoke toxins (yield categories). The machinebased methods approximate human PO 00000 Frm 00041 Fmt 4703 Sfmt 4703 smoking patterns under controlled conditions but may not accurately reflect conditions of actual use, moreover, public health data have not consistently shown differences in health outcomes among smokers of cigarettes of different machine-smoked yield categories. In 2007, the Centers for Disease Control and Prevention (CDC) received OMB approval for a research study designed to elucidate patterns of human smoking behavior, quantify biomarkers of exposure to smoke toxins under conditions of actual use, and assess how smoking behavior modifies the relationship between cigarette yield category, biomarkers of exposure, and measures of cardiovascular reactivity (OMB No. 0920–0736, exp. 3/31/2010). The study was initiated collaboratively by the National Center for Chronic Disease Prevention and Health Promotion (NCCDPHP) and the National E:\FR\FM\31AUN1.SGM 31AUN1 53312 Federal Register / Vol. 75, No. 168 / Tuesday, August 31, 2010 / Notices Center for Environmental Health (NCEH). Information was collected from adult smokers of full-flavor, light and ultralight cigarettes, however, the target number of respondents was not achieved during the initial project period. CDC requests OMB approval to reinstate the information collection in order to meet recruitment goals and complete the data analysis as planned. Changes include a reduction in the number of respondents and a corresponding reduction in the total estimated burden hours. In addition, minor changes will be made to account for changes in cigarette labels, which no longer use descriptors such as fullflavor, light or ultralight. There are no changes to the data collection instruments or the estimated burden per response. Respondents will be asked to participate in a descriptive study of smoking behavior that involves two laboratory visits. Established smokers who are interested in participating will be screened for eligibility during a brief five-minute computer-assisted telephone interview (CATI). We estimate screening approximately 150 individuals annually to yield complete data collection on the annualized goal of 61 respondents. After completing the CATI, individuals who express continued interest in study participation will undergo five additional minutes of eligibility screening at the first laboratory visit. Each respondent who enrolls in the study will make two one-hour visits to an assessment laboratory. The visits will occur on two consecutive days: Visit 1 will be scheduled in the morning of the first day, and Visit 2 will be scheduled in the afternoon of the second day. Samples, measurements, and behavioral information will be collected at each visit. Visit 1 will include biologic sample collection (urine, saliva, breath carbon monoxide), smoking behavior of smoking one cigarette, ventilation hole blocking procedure and breath measurements. Visit 2 will include discussion of quit opportunities if requested, biologic sample collection (urine, saliva, breath carbon monoxide), smoking behavior of smoking one cigarette, ventilation hole blocking procedure and breath measurements. In addition, at Visit 2, each respondent will submit the cigarette butts of all cigarettes smoked since Visit 1 and a completed Smoking Diary Form. The estimated burden for the Smoking Diary Form is ten minutes. The goals of this project are to characterize the range of human smoking behavior for a variety of cigarette categories and machinesmoked yields, and to estimate the levels of biomarkers of exposure with the various cigarette styles. OMB approval is requested for two years. Participation in the study is voluntary. There are no costs to respondents other than their time. The total estimated burden hours are 151. ESTIMATED ANNUALIZED BURDEN HOURS Number of respondents Type of respondent Form name Adult Smokers ......................................................................... CATI Screener ....................... Visit 1 Screener ...................... Smoking Diary ........................ Laboratory Visit ...................... Dated: August 23, 2010. Maryam I. Daneshvar, Reports Clearance Officer, Centers for Disease Control and Prevention. [FR Doc. 2010–21723 Filed 8–30–10; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. FDA–2010–N–0417] srobinson on DSKHWCL6B1PROD with NOTICES Agency Information Collection Activities; Proposed Collection; Comment Request; Experimental Study of Format Variations in the Brief Summary of Direct-to-Consumer Print Advertisements AGENCY: Food and Drug Administration, HHS. ACTION: Notice. The Food and Drug Administration (FDA) is announcing an opportunity for public comment on the proposed collection of certain information by the agency. Under the SUMMARY: VerDate Mar<15>2010 16:33 Aug 30, 2010 Jkt 220001 Paperwork Reduction Act of 1995 (the PRA), Federal agencies are required to publish notice in the Federal Register concerning each proposed collection of information and to allow 60 days for public comment in response to the notice. This notice solicits comments on the Experimental Study of Format Variations in the Brief Summary of Direct-to-Consumer (DTC) Print Advertisements (ads). This study is designed to test different ways of presenting benefit and risk information in the brief summary in DTC print ads. DATES: Submit either electronic or written comments on the collection of information by November 1, 2010. ADDRESSES: Submit electronic comments on the collection of information to https:// www.regulations.gov. Submit written comments on the collection of information to the Division of Dockets Management (HFA–305), Food and Drug Administration, 5630 Fishers Lane, rm. 1061, Rockville, MD 20852. All comments should be identified with the docket number found in brackets in the heading of this document. PO 00000 Frm 00042 Fmt 4703 Sfmt 4703 150 70 61 61 Number of responses per respondent Average burden per response (in hours) 1 1 1 2 5/60 5/60 10/60 1 FOR FURTHER INFORMATION CONTACT: Elizabeth Berbakos, Office of Information Management, Food and Drug Administration, 1350 Piccard Dr., PI50–400B, Rockville, MD 20850, 301– 796–3792, Elizabeth.Berbakos@fda.hhs.gov. Under the PRA (44 U.S.C. 3501–3520), Federal agencies must obtain approval from the Office of Management and Budget (OMB) for each collection of information they conduct or sponsor. ‘‘Collection of information’’ is defined in 44 U.S.C. 3502(3) and 5 CFR 1320.3(c) and includes agency requests or requirements that members of the public submit reports, keep records, or provide information to a third party. Section 3506(c)(2)(A) of the PRA (44 U.S.C. 3506(c)(2)(A)) requires Federal agencies to provide a 60-day notice in the Federal Register concerning each proposed collection of information before submitting the collection to OMB for approval. To comply with this requirement, FDA is publishing notice of the proposed collection of information set forth in this document. SUPPLEMENTARY INFORMATION: E:\FR\FM\31AUN1.SGM 31AUN1

Agencies

[Federal Register Volume 75, Number 168 (Tuesday, August 31, 2010)]
[Notices]
[Pages 53311-53312]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-21723]


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

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Centers for Disease Control and Prevention

[30-Day-10-0736]


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

    Human Smoking Behavior Study--Reinstatement with Change--National 
Center for Chronic Disease Prevention and Health Promotion (NCCDPHP), 
Centers for Disease Control and Prevention (CDC).

Background and Brief Description

    Cigarettes have been ranked as full-flavor, light or ultralight on 
the basis of machine-measured levels of smoke toxins (yield 
categories). The machine-based methods approximate human smoking 
patterns under controlled conditions but may not accurately reflect 
conditions of actual use, moreover, public health data have not 
consistently shown differences in health outcomes among smokers of 
cigarettes of different machine-smoked yield categories.
    In 2007, the Centers for Disease Control and Prevention (CDC) 
received OMB approval for a research study designed to elucidate 
patterns of human smoking behavior, quantify biomarkers of exposure to 
smoke toxins under conditions of actual use, and assess how smoking 
behavior modifies the relationship between cigarette yield category, 
biomarkers of exposure, and measures of cardiovascular reactivity (OMB 
No. 0920-0736, exp. 3/31/2010). The study was initiated collaboratively 
by the National Center for Chronic Disease Prevention and Health 
Promotion (NCCDPHP) and the National

[[Page 53312]]

Center for Environmental Health (NCEH). Information was collected from 
adult smokers of full-flavor, light and ultralight cigarettes, however, 
the target number of respondents was not achieved during the initial 
project period.
    CDC requests OMB approval to reinstate the information collection 
in order to meet recruitment goals and complete the data analysis as 
planned. Changes include a reduction in the number of respondents and a 
corresponding reduction in the total estimated burden hours. In 
addition, minor changes will be made to account for changes in 
cigarette labels, which no longer use descriptors such as full-flavor, 
light or ultralight. There are no changes to the data collection 
instruments or the estimated burden per response.
    Respondents will be asked to participate in a descriptive study of 
smoking behavior that involves two laboratory visits. Established 
smokers who are interested in participating will be screened for 
eligibility during a brief five-minute computer-assisted telephone 
interview (CATI). We estimate screening approximately 150 individuals 
annually to yield complete data collection on the annualized goal of 61 
respondents. After completing the CATI, individuals who express 
continued interest in study participation will undergo five additional 
minutes of eligibility screening at the first laboratory visit.
    Each respondent who enrolls in the study will make two one-hour 
visits to an assessment laboratory. The visits will occur on two 
consecutive days: Visit 1 will be scheduled in the morning of the first 
day, and Visit 2 will be scheduled in the afternoon of the second day. 
Samples, measurements, and behavioral information will be collected at 
each visit. Visit 1 will include biologic sample collection (urine, 
saliva, breath carbon monoxide), smoking behavior of smoking one 
cigarette, ventilation hole blocking procedure and breath measurements. 
Visit 2 will include discussion of quit opportunities if requested, 
biologic sample collection (urine, saliva, breath carbon monoxide), 
smoking behavior of smoking one cigarette, ventilation hole blocking 
procedure and breath measurements. In addition, at Visit 2, each 
respondent will submit the cigarette butts of all cigarettes smoked 
since Visit 1 and a completed Smoking Diary Form. The estimated burden 
for the Smoking Diary Form is ten minutes.
    The goals of this project are to characterize the range of human 
smoking behavior for a variety of cigarette categories and machine-
smoked yields, and to estimate the levels of biomarkers of exposure 
with the various cigarette styles.
    OMB approval is requested for two years. Participation in the study 
is voluntary. There are no costs to respondents other than their time. 
The total estimated burden hours are 151.

                                        Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
                                                                                     Number of    Average burden
          Type of respondent                    Form name            Number of     responses per   per response
                                                                    respondents     respondent      (in hours)
----------------------------------------------------------------------------------------------------------------
Adult Smokers.........................  CATI Screener...........             150               1            5/60
                                        Visit 1 Screener........              70               1            5/60
                                        Smoking Diary...........              61               1           10/60
                                        Laboratory Visit........              61               2               1
----------------------------------------------------------------------------------------------------------------


    Dated: August 23, 2010.
Maryam I. Daneshvar,
Reports Clearance Officer, Centers for Disease Control and Prevention.
[FR Doc. 2010-21723 Filed 8-30-10; 8:45 am]
BILLING CODE 4163-18-P
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