Agency Information Collection Activities: Proposed Collection; Comment Request, 11051-11052 [2017-03190]

Download as PDF Federal Register / Vol. 82, No. 32 / Friday, February 17, 2017 / Notices Dated: February 13, 2017. David Clary, Program Analyst, Office of Federal Advisory Committee Policy. [FR Doc. 2017–03166 Filed 2–16–17; 8:45 am] DEPARTMENT OF HEALTH AND HUMAN SERVICES National Institutes of Health National Institute on Drug Abuse; Notice of Closed Meeting mstockstill on DSK3G9T082PROD with NOTICES Pursuant to section 10(d) of the Federal Advisory Committee Act, as amended (5 U.S.C. App), notice is hereby given of the following meeting. The meeting will be closed to the public in accordance with the provisions set forth in sections 552b(c)(4) and 552b(c)(6), Title 5 U.S.C., as amended. The contract proposals and the discussions could disclose confidential trade secrets or commercial property such as patentable material, and personal information concerning individuals associated with the contract proposals, the disclosure of which would constitute a clearly unwarranted invasion of personal privacy. Name of Committee: National Institute on Drug Abuse Special Emphasis Panel; Analytical Tools and Approaches for (Multidimensional) Scholarly Research Assessment and Decision Support in the Biomedical Enterprise (1214). Date: February 22, 2017. Time: 11:00 a.m. to 5:00 p.m. Agenda: To review and evaluate contract proposals. Place: National Institutes of Health, Neuroscience Center, 6001 Executive Boulevard, Rockville, MD 20852 (Telephone Conference Call). Contact Person: Gerald L. McLaughlin, Ph.D., Scientific Review Officer, Office of Extramural Policy and Review, National Institute on Drug Abuse, NIH, DHHS, 6001 Executive Blvd., Room 4238, MSC 9550, Bethesda, MD 20892–9550, 301–827–5819, gm145a@nih.gov. This notice is being published less than 15 days prior to the meeting due to the timing limitations imposed by the review and funding cycle. (Catalogue of Federal Domestic Assistance Program No.: 93.279, Drug Abuse and Addiction Research Programs, National Institutes of Health, HHS) Dated: February 10, 2017. Natasha M. Copeland, Program Analyst, Office of Federal Advisory Committee Policy. BILLING CODE 4140–01–P VerDate Sep<11>2014 17:38 Feb 16, 2017 Jkt 241001 National Institutes of Health National Institute of Arthritis and Musculoskeletal and Skin Diseases; Notice of Closed Meeting BILLING CODE 4140–01–P [FR Doc. 2017–03169 Filed 2–16–17; 8:45 am] DEPARTMENT OF HEALTH AND HUMAN SERVICES Pursuant to section 10(d) of the Federal Advisory Committee Act, as amended (5 U.S.C. App.), notice is hereby given of the following meeting. The meeting will be closed to the public in accordance with the provisions set forth in sections 552b(c)(4) and 552b(c)(6), Title 5 U.S.C., as amended. The grant applications and the discussions could disclose confidential trade secrets or commercial property such as patentable material, and personal information concerning individuals associated with the grant applications, the disclosure of which would constitute a clearly unwarranted invasion of personal privacy. Name of Committee: Arthritis and Musculoskeletal and Skin Diseases Initial Review Group; Arthritis and Musculoskeletal and Skin Diseases Clinical Trials Review Committee. Date: March 7, 2017. Time: 8:00 a.m. to 5:00 p.m. Agenda: To review and evaluate grant applications. Place: Bethesda Marriott Suites, 6711 Democracy Boulevard, Bethesda, MD 20817. Contact Person: Kathy Salaita, SC.D., Chief, Scientific Review Branch, NIAMS/National Institutes of Health, 6701 Democracy Boulevard, Room 818, Bethesda, MD 20892, Kathy.Salaita@nih.gov. (Catalogue of Federal Domestic Assistance Program Nos. 93.846, Arthritis, Musculoskeletal and Skin Diseases Research, National Institutes of Health, HHS) Dated: February 13, 2017. Sylvia L. Neal, Program Analyst, Office of Federal Advisory Committee Policy [FR Doc. 2017–03162 Filed 2–16–17; 8:45 am] BILLING CODE 4140–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES National Institutes of Health National Institute on Alcohol Abuse and Alcoholism; Notice of Closed Meeting Pursuant to section 10(d) of the Federal Advisory Committee Act, as amended (5 U.S.C. App.), notice is hereby given of the following meeting. The meeting will be closed to the public in accordance with the provisions set forth in sections 552b(c)(4) and 552b(c)(6), Title 5 U.S.C., PO 00000 Frm 00052 Fmt 4703 Sfmt 4703 11051 as amended. The grant applications and the discussions could disclose confidential trade secrets or commercial property such as patentable material, and personal information concerning individuals associated with the grant applications, the disclosure of which would constitute a clearly unwarranted invasion of personal privacy. Name of Committee: National Institute on Alcohol Abuse and Alcoholism Special Emphasis Panel; NIAAA—Review of Member Conflict applications (AA2 & AA3). Date: March 17, 2017. Time: 1:00 p.m. to 3:30 p.m. Agenda: To review and evaluate grant applications. Place: National Institutes of Health, National Institute on Alcohol Abuse and Alcoholism, 5635 Fishers Lane, Bethesda, MD 20892 (Telephone Conference Call). Contact Person: Ranga Srinivas, Ph.D., Chief, Extramural Project Review Branch, National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health, 5365 Fishers Lane, Room 2085, Rockville, MD 20852, (301) 451–2067, srinivar@ mail.nih.gov. (Catalogue of Federal Domestic Assistance Program Nos. 93.271, Alcohol Research Career Development Awards for Scientists and Clinicians; 93.272, Alcohol National Research Service Awards for Research Training; 93.273, Alcohol Research Programs; 93.891, Alcohol Research Center Grants; 93.701, ARRA Related Biomedical Research and Research Support Awards., National Institutes of Health, HHS) Dated: February 13, 2017. Melanie J. Pantoja, Program Analyst, Office of Federal Advisory Committee Policy. [FR Doc. 2017–03161 Filed 2–16–17; 8:45 am] BILLING CODE 4140–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Substance Abuse and Mental Health Services Administration Agency Information Collection Activities: Proposed Collection; Comment Request In compliance with Section 3506(c)(2)(A) of the Paperwork Reduction Act of 1995 concerning the opportunity for public comment on proposed collections of information, the Substance Abuse and Mental Health Services Administration (SAMHSA) will publish periodic summaries of proposed projects. To request more information on the proposed projects or to obtain a copy of the information collection plans, call the SAMHSA Reports Clearance Officer at (240) 276– 1243. Comments are invited on: (a) Whether the proposed collections of information E:\FR\FM\17FEN1.SGM 17FEN1 11052 Federal Register / Vol. 82, No. 32 / Friday, February 17, 2017 / Notices are 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; and (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. Proposed Project: Mandatory Guidelines for Federal Workplace Drug Testing Programs (OMB No. 0930– 0158)—Revision SAMHSA will request OMB approval for the Federal Drug Testing Custody and Control Form (CCF) for federal agency and federally regulated drug testing programs which must comply with the HHS Mandatory Guidelines for Federal Workplace Drug Testing Programs using Urine (82 FR 7920) dated January 23, 2017, and OMB approval for information provided by test facilities (laboratories and Instrumented Initial Test Facilities, IITFs) for the National Laboratory Certification Program (NLCP). The CCF is used by all federal agencies and employers regulated by the Department of Transportation (DOT) and the Nuclear Regulatory Commission (NRC) to document the collection and chain of custody of urine specimens at the collection site, for HHS-certified test facilities to report results, and for Medical Review Officers (MROs) to document and report a verified result. SAMHSA allows the use of the CCF as a paper or electronic form. The current OMB-approved CCF has a May 31, 2017 expiration date. SAMHSA has resubmitted the CCF with minor content revisions to the form for OMB approval. These revisions are: • Remove the checkbox, the letters ‘‘DOT’’, and hash line in front of Specify DOT Agency in Step 1: Completed by collector or employer Representative; Line D: Specify Testing Authority. • Addition of four new analytes (oxycodone, oxymorphone, hydrocodone, and hydromorphone) in Step 5A: Primary Specimen Report— Completed by Test Facility. • Removal of the analyte methylenedioxyethylamphetamine Custody and Control Form: 1 Donor ............................................................................ Collector ........................................................................ Laboratory ..................................................................... IITF ................................................................................ Medical Review Officer ................................................. NLCP Application Form: 2 Laboratory ..................................................................... IITF ................................................................................ Sections B and C—NLCP Inspection Checklist: 3 Laboratory ..................................................................... IITF ................................................................................ Record Keeping: Laboratory ..................................................................... IITF ................................................................................ Total ....................................................................... mstockstill on DSK3G9T082PROD with NOTICES Send comments to Summer King, SAMHSA Reports Clearance Officer, Room 15 E57B, 5600 Fishers Lane, Rockville, MD 20857 OR email a copy to summer.king@samhsa.hhs.gov. Written comments should be received by April 18, 2017. Total number of responses [FR Doc. 2017–03190 Filed 2–16–17; 8:45 am] BILLING CODE 4162–20–P 17:38 Feb 16, 2017 Jkt 241001 5,400,000 5,400,000 5,400,000 0 5,400,000 0.08 0.07 0.05 0 0.05 450,000 360,000 270,000 0 270,000 1 0 1 0 1 0 3 0 3 0 30 0 1 0 30 0 1 0 30 0 30 0 1 0 30 0 250 0 7,500 0 5,400,061 ........................ 5,400,061 ........................ 1,357,533 Federal Emergency Management Agency [Docket ID FEMA–2008–0010] Federal Emergency Management Agency, DHS. ACTION: Committee management; notice of open Federal Advisory Committee Meeting. AGENCY: Frm 00053 Annual burden (hours) 1 1 1 0 1 DEPARTMENT OF HOMELAND SECURITY PO 00000 Burden per response (hours) 5,400,000 5,400,000 5,400,000 0 5,400,000 Board of Visitors for the National Fire Academy Summer King, Statistician. VerDate Sep<11>2014 Responses per respondent Number of respondents Form/respondent (MDEA) in Step 5A: Primary Specimen Report—Completed by Test Facility. Based upon information from federal agencies and from DOT concerning their regulated industries, the number of respondents has been reduced from a total of 6.1 million in 2013 to 5.4 million, which reduces the total burden hours by 188,766. Laboratories and IITFs seeking HHS certification under the NLCP must complete and submit the NLCP application form. The NLCP application form has not been revised compared to the previous form. Prior to an inspection, an HHScertified laboratory or IITF is required to submit specific information regarding its procedures. Collecting this information prior to an inspection allows the inspectors to thoroughly review and understand the testing procedures before arriving for the onsite inspection. The NLCP information checklist has not been revised compared to the previous form. The annual total burden estimates for the CCF, the NLCP application, the NLCP information checklist, and the NLCP recordkeeping requirements are shown in the following table. Fmt 4703 Sfmt 4703 The Board of Visitors for the National Fire Academy (Board) will meet via teleconference on March 16, 2017. The meeting will be open to the public. DATES: The meeting will take place on Thursday, March 16, 2017, from 1:00 to 3:00 p.m. Eastern Daylight Time. Please note that the meeting may close early if the Board has completed its business. ADDRESSES: Members of the public who wish to participate in the teleconference should contact Ruth MacPhail as listed in the FOR FURTHER INFORMATION CONTACT section by close of business SUMMARY: E:\FR\FM\17FEN1.SGM 17FEN1

Agencies

[Federal Register Volume 82, Number 32 (Friday, February 17, 2017)]
[Notices]
[Pages 11051-11052]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2017-03190]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Substance Abuse and Mental Health Services Administration


Agency Information Collection Activities: Proposed Collection; 
Comment Request

    In compliance with Section 3506(c)(2)(A) of the Paperwork Reduction 
Act of 1995 concerning the opportunity for public comment on proposed 
collections of information, the Substance Abuse and Mental Health 
Services Administration (SAMHSA) will publish periodic summaries of 
proposed projects. To request more information on the proposed projects 
or to obtain a copy of the information collection plans, call the 
SAMHSA Reports Clearance Officer at (240) 276-1243.
    Comments are invited on: (a) Whether the proposed collections of 
information

[[Page 11052]]

are 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; and (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.

Proposed Project: Mandatory Guidelines for Federal Workplace Drug 
Testing Programs (OMB No. 0930-0158)--Revision

    SAMHSA will request OMB approval for the Federal Drug Testing 
Custody and Control Form (CCF) for federal agency and federally 
regulated drug testing programs which must comply with the HHS 
Mandatory Guidelines for Federal Workplace Drug Testing Programs using 
Urine (82 FR 7920) dated January 23, 2017, and OMB approval for 
information provided by test facilities (laboratories and Instrumented 
Initial Test Facilities, IITFs) for the National Laboratory 
Certification Program (NLCP).
    The CCF is used by all federal agencies and employers regulated by 
the Department of Transportation (DOT) and the Nuclear Regulatory 
Commission (NRC) to document the collection and chain of custody of 
urine specimens at the collection site, for HHS-certified test 
facilities to report results, and for Medical Review Officers (MROs) to 
document and report a verified result. SAMHSA allows the use of the CCF 
as a paper or electronic form.
    The current OMB-approved CCF has a May 31, 2017 expiration date. 
SAMHSA has resubmitted the CCF with minor content revisions to the form 
for OMB approval. These revisions are:
     Remove the checkbox, the letters ``DOT'', and hash line in 
front of Specify DOT Agency in Step 1: Completed by collector or 
employer Representative; Line D: Specify Testing Authority.
     Addition of four new analytes (oxycodone, oxymorphone, 
hydrocodone, and hydromorphone) in Step 5A: Primary Specimen Report--
Completed by Test Facility.
     Removal of the analyte methylenedioxyethylamphetamine 
(MDEA) in Step 5A: Primary Specimen Report--Completed by Test Facility.
    Based upon information from federal agencies and from DOT 
concerning their regulated industries, the number of respondents has 
been reduced from a total of 6.1 million in 2013 to 5.4 million, which 
reduces the total burden hours by 188,766.
    Laboratories and IITFs seeking HHS certification under the NLCP 
must complete and submit the NLCP application form. The NLCP 
application form has not been revised compared to the previous form.
    Prior to an inspection, an HHS-certified laboratory or IITF is 
required to submit specific information regarding its procedures. 
Collecting this information prior to an inspection allows the 
inspectors to thoroughly review and understand the testing procedures 
before arriving for the onsite inspection. The NLCP information 
checklist has not been revised compared to the previous form.
    The annual total burden estimates for the CCF, the NLCP 
application, the NLCP information checklist, and the NLCP recordkeeping 
requirements are shown in the following table.

----------------------------------------------------------------------------------------------------------------
                                                                                    Burden per
         Form/respondent             Number of     Responses per   Total number      response      Annual burden
                                    respondents     respondent     of responses       (hours)         (hours)
----------------------------------------------------------------------------------------------------------------
Custody and Control Form: \1\
    Donor.......................       5,400,000               1       5,400,000            0.08         450,000
    Collector...................       5,400,000               1       5,400,000            0.07         360,000
    Laboratory..................       5,400,000               1       5,400,000            0.05         270,000
    IITF........................               0               0               0               0               0
    Medical Review Officer......       5,400,000               1       5,400,000            0.05         270,000
NLCP Application Form: \2\
    Laboratory..................               1               1               1               3               3
    IITF........................               0               0               0               0               0
Sections B and C--NLCP
 Inspection Checklist: \3\
    Laboratory..................              30               1              30               1              30
    IITF........................               0               0               0               0               0
Record Keeping:
    Laboratory..................              30               1              30             250           7,500
    IITF........................               0               0               0               0               0
                                 -------------------------------------------------------------------------------
        Total...................       5,400,061  ..............       5,400,061  ..............       1,357,533
----------------------------------------------------------------------------------------------------------------

    Send comments to Summer King, SAMHSA Reports Clearance Officer, 
Room 15 E57B, 5600 Fishers Lane, Rockville, MD 20857 OR email a copy to 
summer.king@samhsa.hhs.gov. Written comments should be received by 
April 18, 2017.

Summer King,
Statistician.
[FR Doc. 2017-03190 Filed 2-16-17; 8:45 am]
BILLING CODE 4162-20-P