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Att 2 60dy FRN
ICR 201609-0920-016 · OMB 0920-0457 · Object 68214901.
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43203 Federal Register / Vol. 81, No. 127 / Friday, July 1, 2016 / Notices of burden hours requested is 1,824 hours. ESTIMATED ANNUALIZED BURDEN HOURS Form name Person with ALS ..................... ALS Case Validation Questions ............................................. ALS Case Registration Form ................................................. Voluntary Survey Modules ..................................................... Disease Progression Survey .................................................. ALS Biorepository Specimen Processing Form ..................... ALS Registry Research Application Form ............................. Annual Update ........................................................................ Chapter/District Outreach Reporting Form ............................ National Office Outreach Reporting Form ............................. Researchers ............................ ALS Service Organization ...... Jeffrey M. Zirger, Health Scientist, Acting Chief, Information Collection Review Office, Office of Scientific Integrity, Office of the Associate Director for Science, Office of the Director, Centers for Disease Control and Prevention. [FR Doc. 2016–15645 Filed 6–30–16; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention [60Day–16–0457: Docket No. CDC–206– 0058] Proposed Data Collection Submitted for Public Comment and Recommendations Centers for Disease Control and Prevention (CDC), Department of Health and Human Services (HHS). ACTION: Notice with comment period. AGENCY: The Centers for Disease Control and Prevention (CDC), as part of its continuing efforts to reduce public burden and maximize the utility of government information, invites the general public and other Federal agencies to take this opportunity to comment on proposed and/or continuing information collections, as required by the Paperwork Reduction Act of 1995. This notice invites comment on Aggregate Reports for Tuberculosis Program Evaluation. The goal of the study is to allow CDC to collect and monitor indicators for key program activities, such as finding tuberculosis infections in recent contacts of cases and in other persons likely to be infected and providing therapy for latent tuberculosis infection in an effort to eliminate Tuberculosis in the United States. SUMMARY: asabaliauskas on DSK3SPTVN1PROD with NOTICES Number of respondents Type of respondents VerDate Sep<11>2014 19:05 Jun 30, 2016 Jkt 238001 Written comments must be received on or before August 30, 2016. ADDRESSES: You may submit comments, identified by Docket No. CDC–2016– 0058 by any of the following methods: • Federal eRulemaking Portal: Regulations.gov. Follow the instructions for submitting comments. • Mail: Leroy A. Richardson, Information Collection Review Office, Centers for Disease Control and Prevention, 1600 Clifton Road NE., MS– D74, Atlanta, Georgia 30329. Instructions: All submissions received must include the agency name and Docket Number. All relevant comments received will be posted without change to Regulations.gov, including any personal information provided. For access to the docket to read background documents or comments received, go to Regulations.gov. DATES: Please note: All public comment should be submitted through the Federal eRulemaking portal (Regulations.gov) or by U.S. mail to the address listed above. To request more information on the proposed project or to obtain a copy of the information collection plan and instruments, contact the Information Collection Review Office, Centers for Disease Control and Prevention, 1600 Clifton Road NE., MS–D74, Atlanta, Georgia 30329; phone: 404–639–7570; Email: omb@cdc.gov. SUPPLEMENTARY INFORMATION: Under the Paperwork Reduction Act of 1995 (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. In addition, the PRA also requires Federal agencies to provide a 60-day notice in the Federal Register concerning each proposed collection of information, including each new proposed collection, each proposed FOR FURTHER INFORMATION CONTACT: PO 00000 Frm 00022 Fmt 4703 Sfmt 4703 1,670 1,500 750 750 325 36 24 135 2 Number of responses per respondent 1 1 1 3 1 1 1 12 12 Average burden per response (in hours) 2/60 10/60 80/60 5/60 30/60 30/60 15/60 5/60 20/60 extension of existing collection of information, and each reinstatement of previously approved information collection before submitting the collection to OMB for approval. To comply with this requirement, we are publishing this notice of a proposed data collection as described below. 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; (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; and (e) estimates of capital or start-up costs and costs of operation, maintenance, and purchase of services to provide information. Burden means the total time, effort, or financial resources expended by persons to generate, maintain, retain, disclose or provide information to or for a Federal agency. This includes the time needed to review instructions; to develop, acquire, install and utilize technology and systems for the purpose of collecting, validating and verifying information, processing and maintaining information, and disclosing and providing information; to train personnel and to be able to respond to a collection of information, to search data sources, to complete and review the collection of information; and to transmit or otherwise disclose the information. E:\FR\FM\01JYN1.SGM 01JYN1 43204 Federal Register / Vol. 81, No. 127 / Friday, July 1, 2016 / Notices Proposed Project Aggregate Reports for Tuberculosis Program Evaluation (0920–0457—Exp. 9–30–2016)—Extension—National Center for HIV/AIDS, Viral Hepatitis, STD, and TB Prevention (NCHHSTP), Centers for Disease Control and Prevention (CDC) Background and Brief Description CDC requests the extension of the Aggregate Reports for Tuberculosis Program Evaluation, previously approved under OMB No. 0920–0457 for 3-years. There are no revisions to the report forms, data definitions, or reporting instructions. To ensure the elimination of tuberculosis in the United States, CDC monitors indicators for key program activities, such as finding tuberculosis infections in recent contacts of cases and in other persons likely to be infected and providing therapy for latent tuberculosis infection. In 2000, CDC implemented two program evaluation reports for annual submission: Aggregate report of followup for contacts of tuberculosis, and Aggregate report of screening and preventive therapy for tuberculosis infection (OMB No. 0920–0457). The respondents for these reports are the 68 state and local tuberculosis control programs receiving federal cooperative agreement funding through the CDC Division of Tuberculosis Elimination (DTBE). These reports emphasize treatment outcomes, high-priority target populations vulnerable to tuberculosis, and programmed electronic report entry, which transitioned to the National Tuberculosis Indicators Project (NTIP), a secure web-based system for program evaluation data, in 2010. No other federal agency collects this type of national tuberculosis data, and the Aggregate report of follow-up for contacts of tuberculosis, and Aggregate report of screening and preventive therapy for tuberculosis infection are the only data source about latent tuberculosis infection for monitoring national progress toward tuberculosis elimination with these activities. CDC provides ongoing assistance in the preparation and utilization of these reports at the local and state levels of public health jurisdiction. CDC also provides respondents with technical support for the NTIP software (Electronic—100%, Use of Electronic Signatures—No). There is no cost to respondents. ESTIMATED ANNUALIZED BURDEN HOURS Type of respondent Form name Data clerks and Program Managers, electronic. Program Managers, manual ..................... Follow-up and Treatment of Contacts to Tuberculosis Cases Form (Att 3a). Follow-up and Treatment of Contacts to Tuberculosis Cases Form (Att 3a). Follow-up and Treatment of Contacts to Tuberculosis Cases Form (Att 3a). Targeted Testing and Treatment for Latent Tuberculosis Infection (Att 3b). Targeted Testing and Treatment for Latent Tuberculosis Infection (Att 3b). Targeted Testing and Treatment for Latent Tuberculosis Infection (Att 3b). Data clerks, (manual) ................................ Data clerks and Program Managers, electronic. Program Managers, (manual) ................... Data clerks, (manual) ................................ Total ................................................... ................................................................... Jeffrey M. Zirger, Health Scientist, Acting Chief, Information Collection Review Office, Office of Scientific Integrity, Office of the Associate Director for Science, Office of the Director, Centers for Disease Control and Prevention. [FR Doc. 2016–15647 Filed 6–30–16; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES asabaliauskas on DSK3SPTVN1PROD with NOTICES Centers for Disease Control and Prevention [60Day–16–16ATI; Docket No. CDC–2016– 0057] Proposed Data Collection Submitted for Public Comment and Recommendations Centers for Disease Control and Prevention (CDC), Department of Health and Human Services (HHS). AGENCY: VerDate Sep<11>2014 19:05 Jun 30, 2016 Jkt 238001 ACTION: Number of responses per respondent 100 1 30/60 50 18 1 30/60 9 18 1 3 54 100 1 30/60 50 18 1 30/60 9 18 1 3 54 .................... ........................ .................... 226 Notice with comment period. The Centers for Disease Control and Prevention (CDC), as part of its continuing efforts to reduce public burden and maximize the utility of government information, invites the general public and other Federal agencies to take this opportunity to comment on proposed and/or continuing information collections, as required by the Paperwork Reduction Act of 1995. This notice invites comment on Development of CDC’s Act Against AIDS Social Marketing Campaigns Targeting Consumers. CDC is requesting approval for revision to the previously approved project to continue testing HIV/AIDS prevention and treatment messages to be included in social marketing campaigns targeting consumers. SUMMARY: Written comments must be received on or before August 30, 2016. DATES: PO 00000 Frm 00023 Fmt 4703 Sfmt 4703 Average burden per response (in hours) Number of respondents Total burden hours You may submit comments, identified by Docket No. CDC–2016– 0057 by any of the following methods: • Federal eRulemaking Portal: Regulation.gov. Follow the instructions for submitting comments. • Mail: Leroy A. Richardson, Information Collection Review Office, Centers for Disease Control and Prevention, 1600 Clifton Road NE., MS– D74, Atlanta, Georgia 30329. Instructions: All submissions received must include the agency name and Docket Number. All relevant comments received will be posted without change to Regulations.gov, including any personal information provided. For access to the docket to read background documents or comments received, go to Regulations.gov. ADDRESSES: Please note: All public comment should be submitted through the Federal eRulemaking portal (Regulations.gov) or by U.S. mail to the address listed above. E:\FR\FM\01JYN1.SGM 01JYN1
| File Type | application/pdf |
| File Title | Att 2 60dy FRN |
| File Modified | 2016-07-01 |
| File Created | 2016-07-01 |