Proposed Collection; 60-day Comment Request; National Institute of Mental Health Recruitment and Milestone Reporting System (NIMH), 31053-31054 [2015-13112]

Download as PDF Federal Register / Vol. 80, No. 104 / Monday, June 1, 2015 / Notices Hurricane Sandy recovery research to the impacted communities. DATES: The 2015 Hurricane Sandy Conference: Translating Research into Practice is scheduled on August 10 from 9 a.m. to 4:30 p.m. EST and on August 11 from 9 a.m. to 12:30 p.m. EST. ADDRESSES: New York University’s Kimmel Center for University Life, 60 Washington Square South, New York City, NY 10010. Registration is required for public attendance. Individuals who wish to attend the meeting should complete the registration via www.PHE.gov/Research2Practice. FOR FURTHER INFORMATION CONTACT: Please contact sciencepreparedness@ hhs.gov for additional information. SUPPLEMENTARY INFORMATION: Background: Shortly after Hurricane Sandy, ASPR, CDC, and NIEHS each funded a series of two-year research grants and training awards under the Disaster Relief Appropriations Act of 2013 (Pub. L. 113–2) that examine the long-term recovery of health systems, communities, and workers in the area of the country hardest hit by the storm. As the projects near completion, ASPR is hosting a public conference to share the research products and outcomes broadly with the impacted communities and other stakeholders. Availability of Materials: The meeting agenda and materials will be posted on www.PHE.gov/Research2Practice prior to the meeting. Registration for the Public Meeting: Information about registration for the meeting is available at www.PHE.gov/ Research2Practice. Dated: May 22, 2015. Nicole Lurie, Assistant Secretary for Preparedness and Response. BILLING CODE 4150–28–P DEPARTMENT OF HEALTH AND HUMAN SERVICES National Institutes of Health Lhorne on DSK2VPTVN1PROD with NOTICES National Institute of Mental Health: 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., as amended. The grant applications and the discussions could disclose confidential trade secrets or commercial 14:50 May 29, 2015 Jkt 235001 Name of Committee: National Institute of Mental Health Special Emphasis Panel; Pilot Effectiveness Studies and Services Research Grants (R34). Date: June 15, 2015. Time: 9 a.m. to 5 p.m. Agenda: To review and evaluate grant applications. Place: Hyatt Regency Bethesda, One Bethesda Metro Center, 7400 Wisconsin Avenue, Bethesda, MD 20814. Contact Person: Karen Gavin-Evans, Ph.D., Scientific Review Officer, Division of Extramural Activities, National Institute of Mental Health, NIH Neuroscience Center, 6001 Executive Boulevard, Room 6153, MSC 9606, Bethesda, MD 20892, 301–451–2356, gavinevanskm@mail.nih.gov. (Catalogue of Federal Domestic Assistance Program No. 93.242, Mental Health Research Grants, National Institutes of Health, HHS) Dated: May 26, 2015. Carolyn A. Baum, Program Analyst, Office of Federal Advisory Committee Policy. [FR Doc. 2015–13049 Filed 5–29–15; 8:45 am] BILLING CODE 4140–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES National Institutes of Health Proposed Collection; 60-day Comment Request; National Institute of Mental Health Recruitment and Milestone Reporting System (NIMH) In compliance with the requirement of Section 3506(c)(2)(A) of the Paperwork Reduction Act of 1995, for opportunity for public comment on proposed data collection projects, the National Institute of Mental Health (NIMH), National Institutes of Health (NIH), will publish periodic summaries of proposed projects to be submitted to the Office of Management and Budget (OMB) for review and approval. Written comments and/or suggestions from the public and affected agencies are invited on one or more of the following points: (1) Whether the proposed collection of information is necessary for the proper performance of the function of the agency, including whether the information will have practical utility; (2) The accuracy of the agency’s estimate of the burden of the proposed collection of information, including the validity of the methodology and assumptions used; (3) Ways to enhance the quality, utility, and clarity of the information to be SUMMARY: [FR Doc. 2015–13050 Filed 5–29–15; 8:45 am] VerDate Sep<11>2014 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. PO 00000 Frm 00057 Fmt 4703 Sfmt 4703 31053 collected; and (4) Ways to minimize the burden of the collection of information on those who are to respond, including the use of appropriate automated, electronic, mechanical, or other technological collection techniques or other forms of information technology. To Submit Comments And For Further Information: To obtain a copy of the data collection plans and instruments, submit comments in writing, or request more information on the proposed project, contact: Keisha Shropshire, NIMH Project Clearance Liaison, Science Policy and Evaluation Branch, OSPPC, NIMH, NIH, Neuroscience Center, 6001 Executive Boulevard, MSC 9667, Rockville Pike, Bethesda, MD 20892, or call 301–443– 4335 or Email your request, including your address to: nimhprapubliccomments@mail.nih.gov. Formal requests for additional plans and instruments must be requested in writing. Comment Due Date: Comments received within 60 days of the date of this publication will receive fullest consideration. Proposed Collection: The National Institute of Mental Health Recruitment Milestone Reporting System (NIMH); REVISION; OMB Control Number 0925– 0697. National Institute of Mental Health, National Institutes of Health. Need and Use of Information Collection: Recruitment Milestone Reporting (RMR) allows NIMH staff to monitor more accurately the required recruitment of participants in NIMHsponsored clinical trials and other clinical research studies that plan to enroll 150 or more human subjects in a single study. Clinical studies can have difficulty recruiting, and accurate and timely reporting is the best way to ensure proper use of the grant funds. Investigators develop a recruitment plan that includes tri-yearly milestones for recruitment of the total study population, and for recruitment of racial and ethnic minority participants. Once recruitment is scheduled to begin, investigators report actual progress on recruitment milestones three times per year, by April 1, August 1, and December 1. Studies that fail to meet their milestones may be requested to provide interim monthly reports. The primary use of this information is to ensure that realistic recruitment targets are established from the onset of a project, and that these targets are met throughout the course of the research. By ensuring timely recruitment into clinical research studies, NIMH can reduce the need to extend timelines or supplement funds in order to complete the research project, and potentially E:\FR\FM\01JNN1.SGM 01JNN1 31054 Federal Register / Vol. 80, No. 104 / Monday, June 1, 2015 / Notices increase efficiency in our funding process. OMB approval is requested for 3 years. There are no costs to respondents other than their time. The total estimated annualized burden hours are 2295. ESTIMATED ANNUALIZED BURDEN HOURS Number of respondents Form Type of respondent NIMH Recruitment Milestone Reporting. NIMH Recruitment Milestone Monthly Report. Principal Investigators/Research Assistant. Principal Investigators/Research Assistant. Dated: May 21, 2015. Keisha L Shropshire, Project Clearance Liaison, NIMH, NIH. [FR Doc. 2015–13112 Filed 5–29–15; 8:45 am] BILLING CODE 4140–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Substance Abuse and Mental Health Services Administration Current List of HHS-Certified Laboratories and Instrumented Initial Testing Facilities Which Meet Minimum Standards To Engage in Urine Drug Testing for Federal Agencies Substance Abuse and Mental Health Services Administration, HHS. ACTION: Notice. AGENCY: The Department of Health and Human Services (HHS) notifies federal agencies of the laboratories and Instrumented Initial Testing Facilities (IITF) currently certified to meet the standards of the Mandatory Guidelines for Federal Workplace Drug Testing Programs (Mandatory Guidelines). The Mandatory Guidelines were first published in the Federal Register on April 11, 1988 (53 FR 11970), and subsequently revised in the Federal Register on June 9, 1994 (59 FR 29908); September 30, 1997 (62 FR 51118); April 13, 2004 (69 FR 19644); November 25, 2008 (73 FR 71858); December 10, 2008 (73 FR 75122); and on April 30, 2010 (75 FR 22809). A notice listing all currently HHScertified laboratories and IITFs is published in the Federal Register during the first week of each month. If any laboratory or IITF certification is suspended or revoked, the laboratory or IITF will be omitted from subsequent lists until such time as it is restored to full certification under the Mandatory Guidelines. If any laboratory or IITF has withdrawn from the HHS National Laboratory Certification Program (NLCP) Lhorne on DSK2VPTVN1PROD with NOTICES SUMMARY: VerDate Sep<11>2014 14:50 May 29, 2015 Jkt 235001 Frm 00058 Fmt 4703 Sfmt 4703 Average time per response (in hours) Annual hour burden 900 3 45/60 2025 40 9 45/60 270 during the past month, it will be listed at the end and will be omitted from the monthly listing thereafter. This notice is also available on the Internet at https://beta.samhsa.gov/ workplace. FOR FURTHER INFORMATION CONTACT: Giselle Hersh, Division of Workplace Programs, SAMHSA/CSAP, Room 7– 1051, One Choke Cherry Road, Rockville, Maryland 20857; 240–276– 2600 (voice), 240–276–2610 (fax). SUPPLEMENTARY INFORMATION: The Mandatory Guidelines were initially developed in accordance with Executive Order 12564 and section 503 of Public Law 100–71. The ‘‘Mandatory Guidelines for Federal Workplace Drug Testing Programs,’’ as amended in the revisions listed above, requires strict standards that laboratories and IITFs must meet in order to conduct drug and specimen validity tests on urine specimens for federal agencies. To become certified, an applicant laboratory or IITF must undergo three rounds of performance testing plus an on-site inspection. To maintain that certification, a laboratory or IITF must participate in a quarterly performance testing program plus undergo periodic, on-site inspections. Laboratories and IITFs in the applicant stage of certification are not to be considered as meeting the minimum requirements described in the HHS Mandatory Guidelines. A HHS-certified laboratory or IITF must have its letter of certification from HHS/SAMHSA (formerly: HHS/NIDA), which attests that it has met minimum standards. In accordance with the Mandatory Guidelines dated November 25, 2008 (73 FR 71858), the following HHScertified laboratories and IITFs meet the minimum standards to conduct drug and specimen validity tests on urine specimens: HHS-Certified Instrumented Initial Testing Facilities: Dynacare Medical Laboratories, 6628 50th Street NW., Edmonton, AB Canada T6B 2N7, 780–784–1190. PO 00000 Frequency of response HHS-Certified Laboratories: ACM Medical Laboratory, Inc., 160 Elmgrove Park, Rochester, NY 14624, 585–429–2264. Aegis Analytical Laboratories, Inc., 345 Hill Ave., Nashville, TN 37210, 615–255–2400, (Formerly: Aegis Sciences Corporation, Aegis Analytical Laboratories, Inc., Aegis Analytical Laboratories). Alere Toxicology Services, 1111 Newton St., Gretna, LA 70053, 504–361– 8989/800–433–3823, (Formerly: Kroll Laboratory Specialists, Inc., Laboratory Specialists, Inc.). Alere Toxicology Services, 450 Southlake Blvd., Richmond, VA 23236, 804–378–9130, (Formerly: Kroll Laboratory Specialists, Inc., Scientific Testing Laboratories, Inc.; Kroll Scientific Testing Laboratories, Inc.). Baptist Medical Center-Toxicology Laboratory, 11401 I–30, Little Rock, AR 72209–7056, 501–202–2783, (Formerly: Forensic Toxicology Laboratory Baptist Medical Center). Clinical Reference Lab, 8433 Quivira Road, Lenexa, KS 66215–2802, 800– 445–6917. DrugScan, Inc., 200 Precision Road, Suite 200, Horsham, PA 19044, 800–235–4890. Dynacare Medical Laboratories *, A Division of the Gamma-Dynacare Laboratory Partnership, 245 Pall Mall Street, London, ONT, Canada N6A 1P4, 519–679–1630. ElSohly Laboratories, Inc., 5 Industrial Park Drive, Oxford, MS 38655, 662– 236–2609. Fortes Laboratories, Inc., 25749 SW Canyon Creek Road, Suite 600, Wilsonville, OR 97070, 503–486– 1023. Laboratory Corporation of America Holdings, 7207 N. Gessner Road, Houston, TX 77040, 713–856–8288/ 800–800–2387. Laboratory Corporation of America Holdings, 69 First Ave., Raritan, NJ 08869, 908–526–2400/800–437– 4986, (Formerly: Roche Biomedical Laboratories, Inc.). E:\FR\FM\01JNN1.SGM 01JNN1

Agencies

[Federal Register Volume 80, Number 104 (Monday, June 1, 2015)]
[Notices]
[Pages 31053-31054]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2015-13112]


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

DEPARTMENT OF HEALTH AND HUMAN SERVICES

National Institutes of Health


Proposed Collection; 60-day Comment Request; National Institute 
of Mental Health Recruitment and Milestone Reporting System (NIMH)

Summary: In compliance with the requirement of Section 3506(c)(2)(A) of 
the Paperwork Reduction Act of 1995, for opportunity for public comment 
on proposed data collection projects, the National Institute of Mental 
Health (NIMH), National Institutes of Health (NIH), will publish 
periodic summaries of proposed projects to be submitted to the Office 
of Management and Budget (OMB) for review and approval.
    Written comments and/or suggestions from the public and affected 
agencies are invited on one or more of the following points: (1) 
Whether the proposed collection of information is necessary for the 
proper performance of the function of the agency, including whether the 
information will have practical utility; (2) The accuracy of the 
agency's estimate of the burden of the proposed collection of 
information, including the validity of the methodology and assumptions 
used; (3) Ways to enhance the quality, utility, and clarity of the 
information to be collected; and (4) Ways to minimize the burden of the 
collection of information on those who are to respond, including the 
use of appropriate automated, electronic, mechanical, or other 
technological collection techniques or other forms of information 
technology.
    To Submit Comments And For Further Information: To obtain a copy of 
the data collection plans and instruments, submit comments in writing, 
or request more information on the proposed project, contact: Keisha 
Shropshire, NIMH Project Clearance Liaison, Science Policy and 
Evaluation Branch, OSPPC, NIMH, NIH, Neuroscience Center, 6001 
Executive Boulevard, MSC 9667, Rockville Pike, Bethesda, MD 20892, or 
call 301-443-4335 or Email your request, including your address to: 
nimhprapubliccomments@mail.nih.gov. Formal requests for additional 
plans and instruments must be requested in writing.
    Comment Due Date: Comments received within 60 days of the date of 
this publication will receive fullest consideration.
    Proposed Collection: The National Institute of Mental Health 
Recruitment Milestone Reporting System (NIMH); REVISION; OMB Control 
Number 0925-0697. National Institute of Mental Health, National 
Institutes of Health.
    Need and Use of Information Collection: Recruitment Milestone 
Reporting (RMR) allows NIMH staff to monitor more accurately the 
required recruitment of participants in NIMH-sponsored clinical trials 
and other clinical research studies that plan to enroll 150 or more 
human subjects in a single study. Clinical studies can have difficulty 
recruiting, and accurate and timely reporting is the best way to ensure 
proper use of the grant funds. Investigators develop a recruitment plan 
that includes tri-yearly milestones for recruitment of the total study 
population, and for recruitment of racial and ethnic minority 
participants. Once recruitment is scheduled to begin, investigators 
report actual progress on recruitment milestones three times per year, 
by April 1, August 1, and December 1. Studies that fail to meet their 
milestones may be requested to provide interim monthly reports. The 
primary use of this information is to ensure that realistic recruitment 
targets are established from the onset of a project, and that these 
targets are met throughout the course of the research. By ensuring 
timely recruitment into clinical research studies, NIMH can reduce the 
need to extend timelines or supplement funds in order to complete the 
research project, and potentially

[[Page 31054]]

increase efficiency in our funding process.
    OMB approval is requested for 3 years. There are no costs to 
respondents other than their time. The total estimated annualized 
burden hours are 2295.

                                        Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
                                                                                   Average time
             Form                    Type of         Number of     Frequency of    per response     Annual hour
                                   respondent       respondents      response       (in hours)        burden
----------------------------------------------------------------------------------------------------------------
NIMH Recruitment Milestone      Principal                    900               3           45/60            2025
 Reporting.                      Investigators/
                                 Research
                                 Assistant.
NIMH Recruitment Milestone      Principal                     40               9           45/60             270
 Monthly Report.                 Investigators/
                                 Research
                                 Assistant.
----------------------------------------------------------------------------------------------------------------


    Dated: May 21, 2015.
Keisha L Shropshire,
Project Clearance Liaison, NIMH, NIH.
[FR Doc. 2015-13112 Filed 5-29-15; 8:45 am]
 BILLING CODE 4140-01-P
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