Agency Forms Undergoing Paperwork Reduction Act Review, 9198-9199 [2016-03821]

Download as PDF 9198 Federal Register / Vol. 81, No. 36 / Wednesday, February 24, 2016 / Notices holding company by acquiring 100 percent of the voting shares of Superior Bancshares, Inc., and thereby indirectly acquire voting shares of Superior Bank, both in Hazelwood, Missouri. Board of Governors of the Federal Reserve System, February 19, 2016. Margaret McCloskey Shanks, Deputy Secretary of the Board. [FR Doc. 2016–03817 Filed 2–23–16; 8:45 am] BILLING CODE 6210–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Agency for Toxic Substances and Disease Registry [Docket No. ATSDR–2016–0003] Availability of Draft Toxicological Profiles; Jet Fuels and 1Bromopropane Agency for Toxic Substances and Disease Registry (ATSDR), Department of Health and Human Services (DHHS). ACTION: Notice of availability, and request for comments. AGENCY: mstockstill on DSK4VPTVN1PROD with NOTICES VerDate Sep<11>2014 17:59 Feb 23, 2016 Jkt 238001 Although a number of key studies for this substance were identified and evaluated during the draft profile development process, this Federal Register notice seeks to solicit any additional studies, particularly unpublished data and ongoing studies. These studies will be evaluated for possible addition to the profile now or in the future. The Toxicological Profiles for Jet Fuels and 1-Bromopropane are available online at https://www.atsdr.cdc.gov/ toxprofiles/index.asp and www.regulations.gov, Docket No. ATSDR–2016–0003. Donna B. Knutson, Acting Director, Office of Policy, Planning and Evaluation, National Center for Environmental Health, and Agency for Toxic Substances and Disease Registry. [FR Doc. 2016–03861 Filed 2–23–16; 8:45 am] BILLING CODE 4163–70–P Ms. Delores Grant, Division of Toxicology and Human Health Sciences, Agency for Toxic Substances and Disease Registry, 1600 Clifton Rd. NE., MS F–57, Atlanta, GA 30329. Phone: (800) 232–4636 or 770–488–3351. DEPARTMENT OF HEALTH AND HUMAN SERVICES The Superfund Amendments and Reauthorization Act (SARA) of 1986 (Pub. L. 99–499) amended the Comprehensive Environmental Response, Compensation, and Liability Act (CERCLA or Superfund). Section 211 of SARA also amended Title 10 of the U.S. Code, creating the Defense Environmental Restoration Program. Section 2704(a) of Title 10 of the U.S. Code directs the Secretary of Defense to notify the Secretary of HHS of not less than 25 of the most commonly found unregulated hazardous substances at defense facilities. The Secretary of HHS is to prepare toxicological profiles of these substances. Each profile is to include an examination, summary, and interpretation of available toxicological information and epidemiologic evaluations. This information is used to ascertain the level of significant human exposure for the substance and the associated health effects. The toxicological profile includes a determination of whether adequate information on the health effects of each substance is available or is in the process of being developed. When adequate information is not available, ATSDR, in cooperation with the National Toxicology Program (NTP), may plan a program of research designed to determine these health effects. Agency Forms Undergoing Paperwork Reduction Act Review FOR FURTHER INFORMATION CONTACT: This notice, prepared by the Agency for Toxic Substances and Disease Registry (ATSDR) for the Department of Defense, announces the availability of two new draft toxicological profile on unregulated hazardous substances for review and comment. All toxicological profiles issued as ‘‘Drafts for Public Comment’’ represent ATSDR’s best efforts to provide important toxicological information on priority hazardous substances. We are seeking public comments and additional information or reports on studies about the health effects of Jet Fuels and 1-Bromopropane for review and potential inclusion in the profile. ATSDR remains committed to providing a public comment period for these documents as a means to best serve public health and our clients. Comments can include additional information or reports on studies about the health effects of Jet Fuels and 1Bromopropane. Although ATSDR will consider key studies for these substances during the profile development process, this Federal Register notice solicits any relevant, additional studies, particularly unpublished data. ATSDR will evaluate the quality and relevance of such data or studies for possible inclusion into the profile. DATES: Written comments on the draft Toxicological Profiles must be received on or before May 24, 2016. SUMMARY: You may submit comments, identified by docket number ATSDR– 2016–0003, by any of the following methods: • Federal eRulemaking Portal: www.regulations.gov. Follow the instructions for submitting comments. • Mail: Division of Toxicology and Human Health Sciences, Agency for Toxic Substances and Disease Registry, 1600 Clifton Rd. NE., MS F–57, Atlanta, GA 30329. Attn: Docket No. ATSDR– 2016–0003. Instructions: All submissions received must include the agency name and docket number for this notice. All relevant comments will be posted without change. Because all public comments regarding ATSDR Toxicological Profiles are available for public inspection, no confidential business information or other confidential information should be submitted in response to this notice. ADDRESSES: SUPPLEMENTARY INFORMATION: PO 00000 Frm 00038 Fmt 4703 Sfmt 4703 Centers for Disease Control and Prevention [30Day–16–0821] The Centers for Disease Control and Prevention (CDC) has submitted the following information collection request to the Office of Management and Budget (OMB) for review and approval in accordance with the Paperwork Reduction Act of 1995. The notice for the proposed information collection is published to obtain comments from the public and affected agencies. Written comments and suggestions from the public and affected agencies concerning the proposed collection of information are encouraged. Your comments should address any of the following: (a) Evaluate whether the proposed collection of information is necessary for the proper performance of the functions of the agency, including whether the information will have practical utility; (b) Evaluate the accuracy of the agencies estimate of the burden of the proposed collection of information, including the validity of the methodology and assumptions used; (c) Enhance the quality, utility, and clarity of the information to be collected; (d) Minimize the burden of the collection of information on those who are to respond, including through the use of appropriate automated, electronic, mechanical, or other technological collection techniques or other forms of information technology, E:\FR\FM\24FEN1.SGM 24FEN1 9199 Federal Register / Vol. 81, No. 36 / Wednesday, February 24, 2016 / Notices e.g., permitting electronic submission of responses; and (e) Assess information collection costs. To request additional information on the proposed project or to obtain a copy of the information collection plan and instruments, call (404) 639–7570 or send an email to omb@cdc.gov. Written comments and/or suggestions regarding the items contained in this notice should be directed to the Attention: CDC Desk Officer, Office of Management and Budget, Washington, DC 20503 or by fax to (202) 395–5806. Written comments should be received within 30 days of this notice. Proposed Project Quarantine Station Illness Response Forms: Airline, Maritime, and Land/ Border Crossing (OMB Control No. 0920–0821; expires 04/30/2016)— Revision—Division of Global Migration and Quarantine, National Center for Emerging Zoonotic and Infectious Diseases, Centers for Disease Control and Prevention (CDC). Background and Brief Description CDC is requesting approval for a revision to this existing information collection with the intent of ensuring that CDC can continue and improve the collection of pertinent information related to communicable disease or deaths that occur aboard conveyances during travel within the United States and into the United States from a foreign country, as authorized under 42 Code of Federal Regulations part 70 and 71, respectively. Concerning routine operations, CDC is adjusting its estimates of respondents and burden associated with the use of the Air Travel, Maritime Conveyance, and Land Travel Illness or Death Investigation forms. • CDC is requesting an increase in the number of respondents to the Air Travel Illness or Death Investigation form, from 1,626 respondents to 1,800. This results in an additional 14 hours of burden per year. • CDC is requesting fewer respondents to the Maritime Conveyance Illness or Death Investigation Form, from 1,873 to 750 reports. This results in a decrease of 93 hours. • CDC is requesting a decrease in the number of respondents to the Land Travel Illness or Death Investigation form, from 259 respondents to 100. This results in a decrease of 14 hours. Also included are changes to account for the end of the entry risk assessment program for travelers entering the United States from the formerly Ebola affected countries. Responses to the United States Travelers Health Declaration and the Ebola Entry Risk Assessment Forms, including the Ill Traveler version, are no longer required for these travelers; therefore, CDC is requesting to remove these forms from this information collection. The changes are as follows: • CDC is requesting the removal of 49,238 respondents to the United States Travel Health Declaration (English: Hard Copy, fillable PDF, electronic portal), resulting in a decrease of 12,310 burden hours. • CDC is requesting the removal of 1,586 respondents to the United States Travel Health Declaration (French translation guide), with a decrease 397 burden hours. • CDC is requesting the removal of 176 respondents for the United States Travel Health Declaration (Arabic translation guide), with a decrease of 44 burden hours. The changes for the Ebola Risk Assessment Form are as follows: • CDC is requesting the removal of 3,447 respondents to the Ebola Risk Assessment Form (English hard copy), and an associated decrease of 862 burden hours. • CDC is requesting the removal of 111 respondents to the Ebola Risk Assessment French translation guide and a decrease of 28 burden hours. • CDC is requesting the removal of 13 respondents to the Ebola Risk Assessment Arabic translation guide, and 3 fewer burden hours. • CDC is requesting the removal of the Ebola Entry Screening Risk Assessment (Ill Traveler Interview), which decreases the number of respondents by 100 and the burden by 25 hours. CDC is no longer requesting the use of this version of the IVR Active Monitoring Survey. Therefore, the following changes are requested: • CDC is requesting the removal of 49,238 respondents to the IVR Active Monitoring Survey (English: Recorded), with 68,933 fewer burden hours. • CDC is requesting the removal of 1,586 respondents to the IVR Active Monitoring Survey (French: Recorded) with a decrease of 2,220 hours of burden. • CDC is requesting the removal of 176 respondents to the IVR Active Monitoring: Arabic translation assistance (no script), with a decrease of 246 burden hours. These adjustments and changes result in a decrease of 85,161 burden hours. CDC requests a total of 2,650 respondents and 221 burden hours annually. The respondents to these information collections are travelers and ship medical personnel. There is no cost to respondents other than the time required to provide the information requested. ESTIMATED ANNUALIZED BURDEN HOURS Number of respondents Respondent Form Traveler ............................................ Ship Medical Personnel ................... Airline Travel Illness or Death Investigation Form ....... Maritime Conveyance Illness or Death Investigation Form. Land Travel Illness or Death Investigation Form ......... mstockstill on DSK4VPTVN1PROD with NOTICES Traveler ............................................ 1 1 5/60 5/60 100 1 5/60 [FR Doc. 2016–03821 Filed 2–23–16; 8:45 am] BILLING CODE 4163–18–P 17:59 Feb 23, 2016 Jkt 238001 PO 00000 Frm 00039 Fmt 4703 Sfmt 9990 E:\FR\FM\24FEN1.SGM Average burden per response (in minutes) 1,800 750 Leroy A. Richardson, 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. VerDate Sep<11>2014 Number of responses per respondent 24FEN1

Agencies

[Federal Register Volume 81, Number 36 (Wednesday, February 24, 2016)]
[Notices]
[Pages 9198-9199]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-03821]


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

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Centers for Disease Control and Prevention

[30Day-16-0821]


Agency Forms Undergoing Paperwork Reduction Act Review

    The Centers for Disease Control and Prevention (CDC) has submitted 
the following information collection request to the Office of 
Management and Budget (OMB) for review and approval in accordance with 
the Paperwork Reduction Act of 1995. The notice for the proposed 
information collection is published to obtain comments from the public 
and affected agencies.
    Written comments and suggestions from the public and affected 
agencies concerning the proposed collection of information are 
encouraged. Your comments should address any of the following: (a) 
Evaluate whether the proposed collection of information is necessary 
for the proper performance of the functions of the agency, including 
whether the information will have practical utility; (b) Evaluate the 
accuracy of the agencies estimate of the burden of the proposed 
collection of information, including the validity of the methodology 
and assumptions used; (c) Enhance the quality, utility, and clarity of 
the information to be collected; (d) Minimize the burden of the 
collection of information on those who are to respond, including 
through the use of appropriate automated, electronic, mechanical, or 
other technological collection techniques or other forms of information 
technology,

[[Page 9199]]

e.g., permitting electronic submission of responses; and (e) Assess 
information collection costs.
    To request additional information on the proposed project or to 
obtain a copy of the information collection plan and instruments, call 
(404) 639-7570 or send an email to omb@cdc.gov. Written comments and/or 
suggestions regarding the items contained in this notice should be 
directed to the Attention: CDC Desk Officer, Office of Management and 
Budget, Washington, DC 20503 or by fax to (202) 395-5806. Written 
comments should be received within 30 days of this notice.

Proposed Project

    Quarantine Station Illness Response Forms: Airline, Maritime, and 
Land/Border Crossing (OMB Control No. 0920-0821; expires 04/30/2016)--
Revision--Division of Global Migration and Quarantine, National Center 
for Emerging Zoonotic and Infectious Diseases, Centers for Disease 
Control and Prevention (CDC).

Background and Brief Description

    CDC is requesting approval for a revision to this existing 
information collection with the intent of ensuring that CDC can 
continue and improve the collection of pertinent information related to 
communicable disease or deaths that occur aboard conveyances during 
travel within the United States and into the United States from a 
foreign country, as authorized under 42 Code of Federal Regulations 
part 70 and 71, respectively.
    Concerning routine operations, CDC is adjusting its estimates of 
respondents and burden associated with the use of the Air Travel, 
Maritime Conveyance, and Land Travel Illness or Death Investigation 
forms.
     CDC is requesting an increase in the number of respondents 
to the Air Travel Illness or Death Investigation form, from 1,626 
respondents to 1,800. This results in an additional 14 hours of burden 
per year.
     CDC is requesting fewer respondents to the Maritime 
Conveyance Illness or Death Investigation Form, from 1,873 to 750 
reports. This results in a decrease of 93 hours.
     CDC is requesting a decrease in the number of respondents 
to the Land Travel Illness or Death Investigation form, from 259 
respondents to 100. This results in a decrease of 14 hours.
    Also included are changes to account for the end of the entry risk 
assessment program for travelers entering the United States from the 
formerly Ebola affected countries. Responses to the United States 
Travelers Health Declaration and the Ebola Entry Risk Assessment Forms, 
including the Ill Traveler version, are no longer required for these 
travelers; therefore, CDC is requesting to remove these forms from this 
information collection. The changes are as follows:
     CDC is requesting the removal of 49,238 respondents to the 
United States Travel Health Declaration (English: Hard Copy, fillable 
PDF, electronic portal), resulting in a decrease of 12,310 burden 
hours.
     CDC is requesting the removal of 1,586 respondents to the 
United States Travel Health Declaration (French translation guide), 
with a decrease 397 burden hours.
     CDC is requesting the removal of 176 respondents for the 
United States Travel Health Declaration (Arabic translation guide), 
with a decrease of 44 burden hours.
    The changes for the Ebola Risk Assessment Form are as follows:
     CDC is requesting the removal of 3,447 respondents to the 
Ebola Risk Assessment Form (English hard copy), and an associated 
decrease of 862 burden hours.
     CDC is requesting the removal of 111 respondents to the 
Ebola Risk Assessment French translation guide and a decrease of 28 
burden hours.
     CDC is requesting the removal of 13 respondents to the 
Ebola Risk Assessment Arabic translation guide, and 3 fewer burden 
hours.
     CDC is requesting the removal of the Ebola Entry Screening 
Risk Assessment (Ill Traveler Interview), which decreases the number of 
respondents by 100 and the burden by 25 hours.

CDC is no longer requesting the use of this version of the IVR Active 
Monitoring Survey. Therefore, the following changes are requested:
     CDC is requesting the removal of 49,238 respondents to the 
IVR Active Monitoring Survey (English: Recorded), with 68,933 fewer 
burden hours.
     CDC is requesting the removal of 1,586 respondents to the 
IVR Active Monitoring Survey (French: Recorded) with a decrease of 
2,220 hours of burden.
 CDC is requesting the removal of 176 respondents to the IVR 
Active Monitoring: Arabic translation assistance (no script), with a 
decrease of 246 burden hours.

    These adjustments and changes result in a decrease of 85,161 burden 
hours.
    CDC requests a total of 2,650 respondents and 221 burden hours 
annually. The respondents to these information collections are 
travelers and ship medical personnel. There is no cost to respondents 
other than the time required to provide the information requested.

                                        Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
                                                                                                      Average
                                                                     Number of       Number of      burden per
              Respondent                          Form              respondents    responses per   response  (in
                                                                                    respondent       minutes)
----------------------------------------------------------------------------------------------------------------
Traveler..............................  Airline Travel Illness             1,800               1            5/60
                                         or Death Investigation
                                         Form.
Ship Medical Personnel................  Maritime Conveyance                  750               1            5/60
                                         Illness or Death
                                         Investigation Form.
Traveler..............................  Land Travel Illness or               100               1            5/60
                                         Death Investigation
                                         Form.
----------------------------------------------------------------------------------------------------------------


Leroy A. Richardson,
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. 2016-03821 Filed 2-23-16; 8:45 am]
 BILLING CODE 4163-18-P
This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.