Agency Forms Undergoing Paperwork Reduction Act Review, 66661-66662 [2016-23340]

Download as PDF Federal Register / Vol. 81, No. 188 / Wednesday, September 28, 2016 / Notices Communications Act of 1934, as amended. Nature and Extent of Confidentiality: Confidentiality is not required with this collection of information. Privacy Impact Assessment: No impact(s). Needs and Uses: Section 73.682(d) of the Commission’s rules incorporates by reference the Advanced Television Systems Committee, Inc. (‘‘ATSC’’) Program System and Information Protocol (‘‘PSIP’’) standard ‘‘A/65C.’’ PSIP data is transmitted along with a TV broadcast station’s digital signal and provides viewers (via their DTV receivers) with information about the station and what is being broadcast, such as program information. The Commission has recognized the utility that the ATSC PSIP standard offers for both broadcasters and consumers (or viewers) of digital television (‘‘DTV’’). ATSC PSIP standard A/65C requires broadcasters to provide detailed programming information when transmitting their broadcast signal. This standard enhances consumers’ viewing experience by providing detailed information about digital channels and programs, such as how to find a program’s closed captions, multiple streams and V-chip information. This standard requires broadcasters to populate the Event Information Tables (‘‘EITs’’) (or program guide) with accurate information about each event (or program) and to update the EIT if more accurate information becomes available. The previous ATSC PSIP standard A/65–B did not require broadcasters to provide such detailed programming information but only general information. Federal Communications Commission. Marlene H. Dortch, Secretary, Office of Secretary. Agreement No.: 012200–004. Title: G6/Zim Transpacific Vessel Sharing Agreement. Parties: American President Lines, Ltd. and APL Co. Pte Ltd. (Operating as one Party); Hapag-Lloyd AG and HapagLloyd USA LLC (Operating as one Party); Hyundai Merchant Marine Co., Ltd.; Mitsui O.S.K. Lines, Ltd.; Nippon Yusen Kaisha; Orient Overseas Container Line Limited.; and Zim Integrated Shipping Services Limited. Filing Party: David F. Smith, Esq.; Cozen O’Connor; 1200 Nineteenth Street NW., Washington, DC 20036. Synopsis: The amendment would expand the geographic scope to include service between certain foreign ports and the U.S. East Coast. It also adds authority for the parties to share vessels and space on strings operated in the Trade by the G6 Lines pursuant to the G6 Alliance Agreement (FMC Agreement No. 012194). The parties have requested Expedited Review. Agreement No.: 012428–001. Title: CMA CGM/ELJSA Asia—USEC Service Space Charter Agreement. Parties: CMA CGM S.A. and ELJSA Line Joint Service Agreement. Filing Party: Paul M. Keane, Esq.; Cichanowicz, Callan, Keane & DeMay, LLP; 50 Main Street, Suite 1045, White Plains, NY, 10606. Synopsis: The amendment would add Taiwan and Panama to the geographic scope of the Agreement. By Order of the Federal Maritime Commission. Dated: September 23, 2016. Karen V. Gregory, Managing Director. [FR Doc. 2016–23401 Filed 9–27–16; 8:45 am] BILLING CODE P DEPARTMENT OF HEALTH AND HUMAN SERVICES [FR Doc. 2016–23381 Filed 9–27–16; 8:45 am] BILLING CODE 6712–01–P Centers for Disease Control and Prevention FEDERAL MARITIME COMMISSION [30Day–16–16TZ] mstockstill on DSK3G9T082PROD with NOTICES Notice of Agreements Filed The Commission hereby gives notice of the filing of the following agreements under the Shipping Act of 1984. Interested parties may submit comments on the agreements to the Secretary, Federal Maritime Commission, Washington, DC 20573, within twelve days of the date this notice appears in the Federal Register. A copy of the agreements is available through the Commission’s Web site (www.fmc.gov) or by contacting the Office of Agreements at (202) 523–5793 or tradeanalysis@fmc.gov. VerDate Sep<11>2014 20:31 Sep 27, 2016 Jkt 238001 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 PO 00000 Frm 00042 Fmt 4703 Sfmt 4703 66661 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.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 Formative Research to Develop HIV Social Marketing Campaigns for Healthcare Providers—New—National Center for HIV/AIDS, Viral Hepatitis, STD, and TB Prevention (NCHHSTP), Centers for Disease Control and Prevention (CDC). Background and Brief Description According to recent estimates, approximately 1.2 million people are living with human immunodeficiency virus (HIV) in the United States, and for the past several years, approximately 50,000 people have been diagnosed annually. It is well-established that certain populations are disproportionately affected by HIV, including men who have sex with men (MSM), African Americans, Hispanics/ Latinos, and transgender communities. In part, to address these health disparities, CDC first published guidelines for HIV testing in health care settings in 2003. CDC updated this guidance to reflect changes in the evidence base in 2006. As the prevention landscape has evolved, so too has CDC’s guidance for health care E:\FR\FM\28SEN1.SGM 28SEN1 66662 Federal Register / Vol. 81, No. 188 / Wednesday, September 28, 2016 / Notices providers. Most recently, CDC published guidelines for health care providers on pre-exposure prophylaxis (PrEP) and recommendations for HIV prevention with adults and adolescents with HIV. Despite clear and compelling guidance from CDC, past studies have shown that patient-provider communication about HIV testing and prevention is uncommon and conversations that do take place tend to be brief. CDC has developed four social marketing campaigns to support patientprovider communication about HIV. These campaigns have made great strides in addressing health care providers’ information needs, thereby building their capacity to discuss HIV prevention with their patients. At this juncture, particularly with the evolving HIV prevention landscape, more data are needed to deepen our understanding of providers’ interpretation and understanding of existing and emergent HIV prevention science; how providers use guidance or evidence-based approaches in their practices generally as well with populations that have been largely overlooked (e.g., transgender individuals); and how to develop new or enrich existing provider materials to make them more informative, appealing, and usable. The three-year study proposes a series of in-depth interviews with 600 healthcare providers (i.e., physicians, physician assistants, and nurses) identified by contractor staff and professional recruiting firms. Data will be collected through one-time, hourlong, individual, in-depth interviews accompanied by a computer-assisted personal interview (total of 1 hour and 15 minutes per person). We anticipate screening 1,200 individuals to obtain 600 individuals who will participate in a 1-hour, in-depth interview and complete a 15-minute computer-assisted personal interview (web-based) survey. All data collections will be conducted only one time. Respondents who will participate in these interviews will be selected purposively to inform the development of appropriate messaging and materials for healthcare providers. Topic areas addressed within the interviews may include HIV prevention, HIV treatment, and linkage and referral to services. Data will be securely stored on password-protected computers and in locked file cabinets. The information gathered through this data collection will allow CDC to develop timely, relevant, clear, and engaging materials that continue to support patient-provider communications related to HIV prevention. Participation of respondents is voluntary, and there is no cost to respondents other than their time. The total estimated annualized burden hours are 950. ESTIMATED ANNUALIZED BURDEN HOURS Number of respondents Type of respondent Form name Health care providers ............. Screener ............................................................................................ Web-based survey ............................................................................ Interviews .......................................................................................... Exploratory guide—Prevention with positives and retention in care Exploratory guide—Transgender health ........................................... Exploratory guide—HIV prevention ................................................... Message testing guide ...................................................................... Concept testing guide ....................................................................... Materials testing guide ...................................................................... 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. 2016–23340 Filed 9–27–16; 8:45 am] BILLING CODE 4163–18–P Food and Drug Administration mstockstill on DSK3G9T082PROD with NOTICES [Docket No. FDA–2007–E–0400] Determination of Regulatory Review Period for Purposes of Patent Extension; IONSYS Food and Drug Administration, HHS. ACTION: Notice. The Food and Drug Administration (FDA) has determined the regulatory review period for SUMMARY: VerDate Sep<11>2014 18:04 Sep 27, 2016 Jkt 238001 Anyone with knowledge that any of the dates as published (in the SUPPLEMENTARY INFORMATION section) are incorrect may submit either electronic or written comments and ask for a redetermination by November 28, 2016. Furthermore, any interested person may petition FDA for a determination regarding whether the applicant for extension acted with due diligence during the regulatory review period by March 27, 2017. See ‘‘Petitions’’ in the SUPPLEMENTARY INFORMATION section for more information. DATES: DEPARTMENT OF HEALTH AND HUMAN SERVICES AGENCY: IONSYS and is publishing this notice of that determination as required by law. FDA has made the determination because of the submission of an application to the Director of the U.S. Patent and Trademark Office (USPTO), Department of Commerce, for the extension of a patent which claims that human drug product. ADDRESSES: You may submit comments as follows: PO 00000 Frm 00043 Fmt 4703 Sfmt 4703 1,200 600 600 50 50 50 150 150 150 Number of responses per respondent Average burden per response (in hours) 1 1 1 1 1 1 1 1 1 10/60 15/60 1 1 1 1 1 1 1 Electronic Submissions Submit electronic comments in the following way: • Federal eRulemaking Portal: http:// www.regulations.gov. Follow the instructions for submitting comments. Comments submitted electronically, including attachments, to http:// www.regulations.gov will be posted to the docket unchanged. Because your comment will be made public, you are solely responsible for ensuring that your comment does not include any confidential information that you or a third party may not wish to be posted, such as medical information, your or anyone else’s Social Security number, or confidential business information, such as a manufacturing process. Please note that if you include your name, contact information, or other information that identifies you in the body of your comments, that information will be posted on http://www.regulations.gov. • If you want to submit a comment with confidential information that you E:\FR\FM\28SEN1.SGM 28SEN1

Agencies

[Federal Register Volume 81, Number 188 (Wednesday, September 28, 2016)]
[Notices]
[Pages 66661-66662]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-23340]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Centers for Disease Control and Prevention

[30Day-16-16TZ]


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, 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

    Formative Research to Develop HIV Social Marketing Campaigns for 
Healthcare Providers--New--National Center for HIV/AIDS, Viral 
Hepatitis, STD, and TB Prevention (NCHHSTP), Centers for Disease 
Control and Prevention (CDC).

Background and Brief Description

    According to recent estimates, approximately 1.2 million people are 
living with human immunodeficiency virus (HIV) in the United States, 
and for the past several years, approximately 50,000 people have been 
diagnosed annually. It is well-established that certain populations are 
disproportionately affected by HIV, including men who have sex with men 
(MSM), African Americans, Hispanics/Latinos, and transgender 
communities.
    In part, to address these health disparities, CDC first published 
guidelines for HIV testing in health care settings in 2003. CDC updated 
this guidance to reflect changes in the evidence base in 2006. As the 
prevention landscape has evolved, so too has CDC's guidance for health 
care

[[Page 66662]]

providers. Most recently, CDC published guidelines for health care 
providers on pre-exposure prophylaxis (PrEP) and recommendations for 
HIV prevention with adults and adolescents with HIV. Despite clear and 
compelling guidance from CDC, past studies have shown that patient-
provider communication about HIV testing and prevention is uncommon and 
conversations that do take place tend to be brief.
    CDC has developed four social marketing campaigns to support 
patient-provider communication about HIV. These campaigns have made 
great strides in addressing health care providers' information needs, 
thereby building their capacity to discuss HIV prevention with their 
patients. At this juncture, particularly with the evolving HIV 
prevention landscape, more data are needed to deepen our understanding 
of providers' interpretation and understanding of existing and emergent 
HIV prevention science; how providers use guidance or evidence-based 
approaches in their practices generally as well with populations that 
have been largely overlooked (e.g., transgender individuals); and how 
to develop new or enrich existing provider materials to make them more 
informative, appealing, and usable.
    The three-year study proposes a series of in-depth interviews with 
600 healthcare providers (i.e., physicians, physician assistants, and 
nurses) identified by contractor staff and professional recruiting 
firms. Data will be collected through one-time, hour-long, individual, 
in-depth interviews accompanied by a computer-assisted personal 
interview (total of 1 hour and 15 minutes per person). We anticipate 
screening 1,200 individuals to obtain 600 individuals who will 
participate in a 1-hour, in-depth interview and complete a 15-minute 
computer-assisted personal interview (web-based) survey. All data 
collections will be conducted only one time. Respondents who will 
participate in these interviews will be selected purposively to inform 
the development of appropriate messaging and materials for healthcare 
providers. Topic areas addressed within the interviews may include HIV 
prevention, HIV treatment, and linkage and referral to services. Data 
will be securely stored on password-protected computers and in locked 
file cabinets.
    The information gathered through this data collection will allow 
CDC to develop timely, relevant, clear, and engaging materials that 
continue to support patient-provider communications related to HIV 
prevention. Participation of respondents is voluntary, and there is no 
cost to respondents other than their time.
    The total estimated annualized burden hours are 950.

                                        Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
                                                                                         Number of     Average
                                                                           Number of     responses    burden per
          Type of respondent                        Form name             respondents       per        response
                                                                                        respondent    (in hours)
----------------------------------------------------------------------------------------------------------------
Health care providers.................  Screener........................        1,200             1        10/60
                                        Web-based survey................          600             1        15/60
                                        Interviews......................          600             1            1
                                        Exploratory guide--Prevention              50             1            1
                                         with positives and retention in
                                         care.
                                        Exploratory guide--Transgender             50             1            1
                                         health.
                                        Exploratory guide--HIV                     50             1            1
                                         prevention.
                                        Message testing guide...........          150             1            1
                                        Concept testing guide...........          150             1            1
                                        Materials testing guide.........          150             1            1
----------------------------------------------------------------------------------------------------------------


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. 2016-23340 Filed 9-27-16; 8:45 am]
 BILLING CODE 4163-18-P