Proposed Data Collection Submitted for Public Comment and Recommendations, 42096-42098 [2017-18814]

Download as PDF asabaliauskas on DSKBBXCHB2PROD with NOTICES 42096 Federal Register / Vol. 82, No. 171 / Wednesday, September 6, 2017 / Notices productivity of the program; and (3) increase transparency so issues are identified early in the process. Information about this program is available at: https://www.epa.gov/iris. Availability of Meeting Materials: Additional background on this SAB activity, the meeting agenda, and other materials for the meeting will be posted on the SAB Web site at https:// www.epa.gov/sab. Procedures for Providing Public Input: Public comment for consideration by EPA’s federal advisory committees and panels has a different purpose from public comment provided to EPA program offices. Therefore, the process for submitting comments to a federal advisory committee is different from the process used to submit comments to an EPA program office. Federal advisory committees and panels, including scientific advisory committees, provide independent advice to the EPA. Members of the public can submit relevant comments pertaining to the meeting materials or the group conducting this SAB activity. Input from the public to the SAB will have the most impact if it consists of comments that provide specific scientific or technical information or analysis for SAB committees and panels to consider or if it relates to the clarity or accuracy of the technical information. Members of the public wishing to provide comment should contact the DFO directly. Oral Statements: In general, individuals or groups requesting an oral presentation at a public meeting will be limited to five minutes per speaker. Interested parties wishing to provide comments should contact Dr. Suhair Shallal, DFO (preferably via email) at the contact information noted above by September 20, 2017, to be placed on the list of public speakers for the meeting. Written Statements: Written statements will be accepted throughout the advisory process; however, for timely consideration by Committee members, statements should be supplied to the DFO (preferably via email) at the contact information noted above by September 20, 2017. It is the SAB Staff Office general policy to post written comments on the Web page for the advisory meeting. Submitters are requested to provide an unsigned version of each document because the SAB Staff Office does not publish documents with signatures on its Web sites. Members of the public should be aware that their personal contact information, if included in any written comments, may be posted to the SAB Web site. Copyrighted material will not VerDate Sep<11>2014 17:37 Sep 05, 2017 Jkt 241001 be posted without explicit permission of the copyright holder. Accessibility: For information on access or services for individuals with disabilities, please contact Dr. Suhair Shallal at (202) 564–0257 or at shallal.suhair@epa.gov. To request accommodation of a disability, please contact Dr. Shallal preferably at least ten days prior to the meeting, to give EPA as much time as possible to process your request. Dated: August 21, 2017. Christopher Zarba, Director, EPA Science Advisory Board Staff Office. [FR Doc. 2017–18764 Filed 9–5–17; 8:45 am] BILLING CODE 6560–50–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention [60-Day–17–17AUQ; Docket No. CDC–2017– 0064] 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 Mobile Proximity Initial User Feedback information collection project. DATES: Written comments must be received on or before November 6, 2017. ADDRESSES: You may submit comments, identified by Docket No. CDC–2017– 0064 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 SUMMARY: PO 00000 Frm 00041 Fmt 4703 Sfmt 4703 to Regulations.gov, including any personal information provided. For access to the docket to read background documents or comments received, go to Regulations.gov. 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. FOR FURTHER INFORMATION CONTACT: To request more information on the proposed project or to obtain a copy of the information collection plan and instruments, contact Leroy A. Richardson, 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 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 E:\FR\FM\06SEN1.SGM 06SEN1 Federal Register / Vol. 82, No. 171 / Wednesday, September 6, 2017 / Notices 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. Proposed Project Mobile Proximity Initial User Feedback—New—National Institute for Occupational Safety and Health (NIOSH), Centers for Disease Control and Prevention (CDC). asabaliauskas on DSKBBXCHB2PROD with NOTICES Background and Brief Description As a part of The National Institute for Occupational Safety and Health (NIOSH) Pittsburgh Mining Research Division (PMRD) project Design of Proximity Systems for Underground Mobile Equipment, NIOSH researchers are looking to assess the current state of proximity systems being used by industry. In conjunction with performance based testing, researchers are examining the human factors aspects of the systems and their implementations. NIOSH is requesting a three-year OMB approval to collect information. Striking, pinning, and crushing injuries are a serious concern in underground coal mining, especially around mobile equipment. Between 2010 and 2014 powered haulage accounted for 24 of the 110 underground coal fatalities (NIOSH, 2016). During that same time period, the Mine Safety and Health Administration (MSHA) determined that up to 9 of these fatalities were striking, pinning, or crushing accidents that may have been prevented by proximity detection systems on coal haulage machines or scoops (MSHA, 2016a). Following the final rule requiring proximity detection systems on continuous mining machines, on September 2, 2015, MSHA published a proposed rule requiring proximity systems on mobile machines in underground coal mines (MSHA, 2015a; 2015b). Though the rule is still under development, MSHA reported that by June of 2015, 155 of approximately 2,116 coal haulage machines and scoops had been 42097 study identified a need for additional research related to the performance of proximity detection systems on mobile equipment. Even though the pilot study and related, subsequent studies offer findings, which may potentially compliment findings from the proposed study, these studies were not specifically designed to focus on human factors. Conversely, the proposed study focuses on human factors influencing the safety and effectiveness of proximity systems installed on underground mobile equipment. The proposed research study involves conducting semi-structured interviews and optional observations of regularly assigned job duties with a maximum of 250 mining crew members. To recruit the mines, operators will be contacted. The recruitment conversation is expected to last 15 minutes. Up to 250, 10-minute, semi-structured interviews will be conducted to collect workers’ experiences with and perspectives on current proximity detection systems on mobile haulage equipment. To capture a variety of perspectives, various members of the section crews will be invited to participate in the interviews. Prior to the interview, miners will be read a verbal informed consent and asked to give verbal affirmation that they agree to participate in the study. Workers that do not wish to participate will be given the opportunity to leave. Following the interviews, a subset of mine workers will be observed as a section crew of 7 to 13 individuals performing their normal duties for an hour during their shift. The observation component is optional for the individuals. Since the participant will be performing regular job duties during the observation, this does not require any additional time from the participant. To observe crew members in a designated section, researchers will obtain verbal consent from all miners who may be observed. If a crew member working in a designated section chooses to be excluded from the study, the section will not be observed. Observation will focus on general behavior with and around the proximity system. The total estimated time burden is 44 hours. There are no costs to respondents other than their time. equipped with proximity detection systems (MSHA, 2016b). On January 9 of 2017, MSHA reopened the comment period for equipping underground mobile machines with proximity detection systems. MSHA reopened the comment period for two key reasons. First, MSHA reopened the comment period to explore any additional comments raised during or following the closing of the original comment period. Second, MSHA reopened the comment period to allow for comments on a field-report on proximity detection system utilization in South Africa, which was conducted following the original comment period and presented at the June 22, 2016 NIOSH Proximity Detection Partnership Meeting. Some of concerns raised were related to the potential risks that proximity detection systems on mobile equipment might pose for mine workers. The comments included risk such as those associated with performing routine maintenance and troubleshooting tasks, machine movements, which may result in pinning, crushing, or striking accidents, and sudden equipment stops which may harm machine operators. NIOSH researchers are looking to determine the critical use cases for proximity systems on mobile equipment in underground mines. Researchers would like to answer the following questions: (1) In which situations do proximity detection systems on mobile haulage hinder normal operation? and (2) in which situations do proximity detection systems on mobile haulage endanger miners? Researchers are also interested in determining what factors should be considered related to human machine interfaces when implementing proximity systems on mobile equipment in underground mines. Specifically, researchers hope to answer the following questions: (1) What is the expected behavior of a proximity detection system on mobile haulage? and (2) What are the desired user features of a proximity detection system on mobile haulage? Previously, NIOSH conducted a pilot study on proximity detection systems on mobile equipment used in underground coal mines. The pilot study involved determining the required stopping distances and times for mobile equipment. Findings from the pilot ESTIMATED ANNUALIZED BURDEN HOURS Form name Mine Operators ................................. Mine Recruitment Script ................... VerDate Sep<11>2014 17:37 Sep 05, 2017 Jkt 241001 PO 00000 Frm 00042 Number of responses per respondent Number of respondents Type of respondents Fmt 4703 Sfmt 4703 6 E:\FR\FM\06SEN1.SGM 1 06SEN1 Average burden per response (in hours) 15/60 Total burden (in hours) 2 42098 Federal Register / Vol. 82, No. 171 / Wednesday, September 6, 2017 / Notices ESTIMATED ANNUALIZED BURDEN HOURS—Continued Number of respondents Number of responses per respondent Average burden per response (in hours) Total burden (in hours) Type of respondents Form name Crew Members .................................. Interview protocol ............................. 250 1 10/60 42 Total ........................................... ........................................................... ........................ ........................ ........................ 44 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. DEPARTMENT OF HEALTH AND HUMAN SERVICES [FR Doc. 2017–18814 Filed 9–5–17; 8:45 am] Development of a List of Pre-Dietary Supplement Health and Education Act Dietary Ingredients; Public Meeting; Request for Comments BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Notice of public meeting; request for comments. ACTION: Food and Drug Administration, HHS. Notice; correction. The Food and Drug Administration (FDA) is correcting a document entitled ‘‘B. Braun Medical, Inc.; Withdrawal of Approval of Three New Drug Applications and One Abbreviated New Drug Application’’ that appeared in the Federal Register of August 3, 2017 (82 FR 36150). The document was published with the incorrect docket number. This document corrects that error. FOR FURTHER INFORMATION CONTACT: Lisa Granger, Office of Policy, Food and Drug Administration, Bldg. 32, Rm. 3330, Silver Spring, MD 20993–0002, 301– 796–9115. SUPPLEMENTARY INFORMATION: In the Federal Register of Thursday, August 3, 2017, in FR Doc. 2017–16377, on page 36150, the following correction is made: 1. On page 36150, in the second column, in the header of the document, ‘‘Docket No. FDA–2017–N–0002’’ is corrected to read ‘‘Docket No. FDA– 2017–N–4642’’. asabaliauskas on DSKBBXCHB2PROD with NOTICES Dated: August 28, 2017. Anna K. Abram, Deputy Commissioner for Policy, Planning, Legislation, and Analysis. [FR Doc. 2017–18813 Filed 9–5–17; 8:45 am] BILLING CODE 4164–01–P VerDate Sep<11>2014 17:37 Sep 05, 2017 Jkt 241001 The Food and Drug Administration (FDA or we) is announcing the following public meeting entitled ‘‘Development of a List of Pre-DSHEA Dietary Ingredients.’’ The purpose of the meeting is to give interested stakeholders an opportunity to discuss issues related to FDA’s future development of such a list. DATES: The public meeting will be held on October 3, 2017, from 8 a.m. to 5 p.m. Submit either electronic or written comments on this public meeting by December 4, 2017. See the SUPPLEMENTARY INFORMATION section for registration date and information. ADDRESSES: The public meeting will be held at FDA’s Center for Food Safety and Applied Nutrition, Wiley Auditorium, 5001 Campus Dr., College Park, MD 20740. You may submit comments as follows. Please note that late, untimely filed comments will not be considered. Electronic comments must be submitted on or before December 4, 2017. The https://www.regulations.gov electronic filing system will accept comments until midnight Eastern Time at the end of December 4, 2017. Comments received by mail/hand delivery/courier (for written/paper submissions) will be considered timely if they are postmarked or the delivery service acceptance receipt is on or before that date. SUMMARY: B. Braun Medical, Inc.; Withdrawal of Approval of Three New Drug Applications and One Abbreviated New Drug Application; Correction SUMMARY: Food and Drug Administration, HHS. [Docket No. FDA–2017–N–4642] ACTION: [Docket No. FDA–2017–N–4625] AGENCY: Food and Drug Administration AGENCY: Food and Drug Administration Electronic Submissions Submit electronic comments in the following way: • Federal eRulemaking Portal: https://www.regulations.gov. Follow the PO 00000 Frm 00043 Fmt 4703 Sfmt 4703 instructions for submitting comments. Comments submitted electronically, including attachments, to https:// 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 https://www.regulations.gov. • If you want to submit a comment with confidential information that you do not wish to be made available to the public, submit the comment as a written/paper submission and in the manner detailed (see ‘‘Written/Paper Submissions’’ and ‘‘Instructions’’). Written/Paper Submissions Submit written/paper submissions as follows: • Mail/Hand delivery/Courier (for written/paper submissions): Dockets Management Staff (HFA–305), Food and Drug Administration, 5630 Fishers Lane, Rm. 1061, Rockville, MD 20852. • For written/paper comments submitted to the Dockets Management Staff, FDA will post your comment, as well as any attachments, except for information submitted, marked and identified, as confidential, if submitted as detailed in ‘‘Instructions.’’ Instructions: All submissions received must include the Docket No. FDA– 2017–N–4625 for ‘‘Development of a List of Pre-DSHEA Dietary Ingredients; Public Meeting; Request for Comments.’’ Received comments, those filed in a timely manner (see ADDRESSES), will be placed in the docket and, except for those submitted as ‘‘Confidential Submissions,’’ publicly viewable at https://www.regulations.gov or at the Dockets Management Staff between 9 a.m. and 4 p.m., Monday through Friday. • Confidential Submissions—To submit a comment with confidential E:\FR\FM\06SEN1.SGM 06SEN1

Agencies

[Federal Register Volume 82, Number 171 (Wednesday, September 6, 2017)]
[Notices]
[Pages 42096-42098]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2017-18814]


=======================================================================
-----------------------------------------------------------------------

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Centers for Disease Control and Prevention

[60-Day-17-17AUQ; Docket No. CDC-2017-0064]


Proposed Data Collection Submitted for Public Comment and 
Recommendations

AGENCY: Centers for Disease Control and Prevention (CDC), Department of 
Health and Human Services (HHS).

ACTION: Notice with comment period.

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

SUMMARY: 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 Mobile Proximity 
Initial User Feedback information collection project.

DATES: Written comments must be received on or before November 6, 2017.

ADDRESSES: You may submit comments, identified by Docket No. CDC-2017-
0064 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.
    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.

FOR FURTHER INFORMATION CONTACT: To request more information on the 
proposed project or to obtain a copy of the information collection plan 
and instruments, contact Leroy A. Richardson, 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 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

[[Page 42097]]

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.

Proposed Project

    Mobile Proximity Initial User Feedback--New--National Institute for 
Occupational Safety and Health (NIOSH), Centers for Disease Control and 
Prevention (CDC).

Background and Brief Description

    As a part of The National Institute for Occupational Safety and 
Health (NIOSH) Pittsburgh Mining Research Division (PMRD) project 
Design of Proximity Systems for Underground Mobile Equipment, NIOSH 
researchers are looking to assess the current state of proximity 
systems being used by industry. In conjunction with performance based 
testing, researchers are examining the human factors aspects of the 
systems and their implementations. NIOSH is requesting a three-year OMB 
approval to collect information.
    Striking, pinning, and crushing injuries are a serious concern in 
underground coal mining, especially around mobile equipment. Between 
2010 and 2014 powered haulage accounted for 24 of the 110 underground 
coal fatalities (NIOSH, 2016). During that same time period, the Mine 
Safety and Health Administration (MSHA) determined that up to 9 of 
these fatalities were striking, pinning, or crushing accidents that may 
have been prevented by proximity detection systems on coal haulage 
machines or scoops (MSHA, 2016a). Following the final rule requiring 
proximity detection systems on continuous mining machines, on September 
2, 2015, MSHA published a proposed rule requiring proximity systems on 
mobile machines in underground coal mines (MSHA, 2015a; 2015b). Though 
the rule is still under development, MSHA reported that by June of 
2015, 155 of approximately 2,116 coal haulage machines and scoops had 
been equipped with proximity detection systems (MSHA, 2016b).
    On January 9 of 2017, MSHA reopened the comment period for 
equipping underground mobile machines with proximity detection systems. 
MSHA reopened the comment period for two key reasons. First, MSHA 
reopened the comment period to explore any additional comments raised 
during or following the closing of the original comment period. Second, 
MSHA reopened the comment period to allow for comments on a field-
report on proximity detection system utilization in South Africa, which 
was conducted following the original comment period and presented at 
the June 22, 2016 NIOSH Proximity Detection Partnership Meeting. Some 
of concerns raised were related to the potential risks that proximity 
detection systems on mobile equipment might pose for mine workers. The 
comments included risk such as those associated with performing routine 
maintenance and troubleshooting tasks, machine movements, which may 
result in pinning, crushing, or striking accidents, and sudden 
equipment stops which may harm machine operators.
    NIOSH researchers are looking to determine the critical use cases 
for proximity systems on mobile equipment in underground mines. 
Researchers would like to answer the following questions: (1) In which 
situations do proximity detection systems on mobile haulage hinder 
normal operation? and (2) in which situations do proximity detection 
systems on mobile haulage endanger miners? Researchers are also 
interested in determining what factors should be considered related to 
human machine interfaces when implementing proximity systems on mobile 
equipment in underground mines. Specifically, researchers hope to 
answer the following questions: (1) What is the expected behavior of a 
proximity detection system on mobile haulage? and (2) What are the 
desired user features of a proximity detection system on mobile 
haulage?
    Previously, NIOSH conducted a pilot study on proximity detection 
systems on mobile equipment used in underground coal mines. The pilot 
study involved determining the required stopping distances and times 
for mobile equipment. Findings from the pilot study identified a need 
for additional research related to the performance of proximity 
detection systems on mobile equipment. Even though the pilot study and 
related, subsequent studies offer findings, which may potentially 
compliment findings from the proposed study, these studies were not 
specifically designed to focus on human factors. Conversely, the 
proposed study focuses on human factors influencing the safety and 
effectiveness of proximity systems installed on underground mobile 
equipment.
    The proposed research study involves conducting semi-structured 
interviews and optional observations of regularly assigned job duties 
with a maximum of 250 mining crew members. To recruit the mines, 
operators will be contacted. The recruitment conversation is expected 
to last 15 minutes.
    Up to 250, 10-minute, semi-structured interviews will be conducted 
to collect workers' experiences with and perspectives on current 
proximity detection systems on mobile haulage equipment. To capture a 
variety of perspectives, various members of the section crews will be 
invited to participate in the interviews.
    Prior to the interview, miners will be read a verbal informed 
consent and asked to give verbal affirmation that they agree to 
participate in the study. Workers that do not wish to participate will 
be given the opportunity to leave. Following the interviews, a subset 
of mine workers will be observed as a section crew of 7 to 13 
individuals performing their normal duties for an hour during their 
shift. The observation component is optional for the individuals. Since 
the participant will be performing regular job duties during the 
observation, this does not require any additional time from the 
participant. To observe crew members in a designated section, 
researchers will obtain verbal consent from all miners who may be 
observed. If a crew member working in a designated section chooses to 
be excluded from the study, the section will not be observed. 
Observation will focus on general behavior with and around the 
proximity system.
    The total estimated time burden is 44 hours. There are no costs to 
respondents other than their time.

                                        Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
                                                                     Number of    Average burden
      Type of respondents           Form name        Number of     responses per   per response    Total burden
                                                    respondents     respondent      (in hours)      (in hours)
----------------------------------------------------------------------------------------------------------------
Mine Operators................  Mine Recruitment               6               1           15/60               2
                                 Script.

[[Page 42098]]

 
Crew Members..................  Interview                    250               1           10/60              42
                                 protocol.
                                                 ---------------------------------------------------------------
    Total.....................  ................  ..............  ..............  ..............              44
----------------------------------------------------------------------------------------------------------------


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. 2017-18814 Filed 9-5-17; 8:45 am]
 BILLING CODE 4163-18-P
This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.