Agency Information Collection Activities: Proposed Collection; Comment Request, 22999-23001 [2016-09020]

Download as PDF 22999 Federal Register / Vol. 81, No. 75 / Tuesday, April 19, 2016 / Notices (Catalogue of Federal Domestic Assistance Program Nos. 93.859, Pharmacology, Physiology, and Biological Chemistry Research; 93.350, B—Cooperative Agreements; 93.859, Biomedical Research and Research Training, National Institutes of Health, HHS) Dated: April 13, 2016. David Clary, Program Analyst, Office of Federal Advisory Committee Policy. [FR Doc. 2016–08992 Filed 4–18–16; 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 mstockstill on DSK4VPTVN1PROD with NOTICES In compliance with section 3506(c)(2)(A) of the Paperwork Reduction Act of 1995 concerning 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 on (240) 276– 1243. Comments are invited on: (a) Whether the proposed collections of information 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: Opioid Drugs in Maintenance and Detoxification Treatment of Opioid Dependence—42 CFR part 8 (OMB No. 0930–0206) and Opioid Treatment Programs (OTPs)— Revision 42 CFR part 8 establishes a certification program managed by SAMHSA’s Center for Substance Abuse Treatment (CSAT). The regulation requires that Opioid Treatment Programs (OTPs) be certified. ‘‘Certification’’ is the process by which SAMHSA determines that an OTP is qualified to provide opioid treatment under the Federal opioid treatment standards established by the Secretary of Health and Human Services. To become certified, an OTP must be accredited by a SAMHSA-approved accreditation body. The regulation also provides standards for such services as individualized treatment planning, increased medical supervision, and assessment of patient outcomes. This submission seeks continued approval of the information collection requirements in the regulation and of the forms used in implementing the regulation. SAMHSA currently has approval for the Application for Certification to Use Opioid Drugs in a Treatment Program Under 42 CFR 8.11 (Form SMA–162); the Application for Approval as Accreditation Body Under 42 CFR 8.3(b) (Form SMA–163); and the Exception Request and Record of Justification Under 42 CFR 8.12 (Form SMA–168), which may be used by physicians when there is a patient care situation in which the physician must make a treatment decision that differs from the treatment regimen required by the regulation. Form SMA–168 is a simplified, standardized form to facilitate the documentation, request, and approval process for exceptions. SAMHSA believes that the recordkeeping requirements in the regulation are customary and usual practices within the medical and rehabilitative communities and has not calculated a response burden for them. The recordkeeping requirements set forth in 42 CFR 8.4, 8.11, and 8.12 include maintenance of the following: 5year retention by accreditation bodies of certain records pertaining to accreditation, and documentation by an OTP of the following: A patient’s medical examination when admitted to treatment, a patient’s history, a treatment plan, any prenatal support provided to the patient, justification of unusually large initial doses, changes in a patient’s dosage schedule, justification of unusually large daily doses, the rationale for decreasing a patient’s clinic attendance, and documentation of physiologic dependence. The rule also includes requirements that OTPs and accreditation organizations disclose information. For example, 42 CFR 8.12(e)(1) requires that a physician explain the facts concerning the use of opioid drug treatment to each patient. This type of disclosure is considered to be consistent with the common medical practice and is not considered an additional burden. Further, the rule requires, under Sec. 8.4(i)(1) that accreditation organizations shall make public their fee structure; this type of disclosure is standard business practice and is not considered a burden. A number of changes have been made to the forms. Forms have been reworded for clarification, updated with current SAMHSA mailing and web-submission information, and a few additional fields have been provided for clarity and for providers to best explain their services (e.g., expanding the former global patient census in the SMA–162 to request patient census by drug type— methadone, buprenorphine, naltrexone, or other) and the needs of their patients (e.g., including urinalysis results on the SMA–168 and adding ‘‘weather crisis’’ as a standard option for physician justification of the requested exception). Amendments also include the removal of information pertaining to faxing the forms to SAMHSA, as this is no longer an acceptable form of submission. The burden hours have increased slightly (by 28% or approximately 639 hours) due to an increase in the number of facilities accredited and certified by SAMHSA since the previous submissions of these forms. The forms are available online with a unique feature for both the SMA–162 and SMA–168 that pre-populates certain information within the form. This in turn reduces the program’s time spent filling out the forms as well as the staff time spent on processing it. The tables that follow summarize the annual reporting burden associated with the regulation, including burden associated with the forms. ESTIMATED ANNUAL REPORTING REQUIREMENT BURDEN FOR ACCREDITATION BODIES Number of respondents 42 CFR citation Purpose 8.3(b)(1–11) ......... Initial approval (SMA–163) ................ VerDate Sep<11>2014 18:02 Apr 18, 2016 Jkt 238001 PO 00000 Frm 00036 Responses/ respondent 1 Fmt 4703 Sfmt 4703 Total responses 1 E:\FR\FM\19APN1.SGM Hours/ response 1 19APN1 6.00 Total hours 6.00 23000 Federal Register / Vol. 81, No. 75 / Tuesday, April 19, 2016 / Notices ESTIMATED ANNUAL REPORTING REQUIREMENT BURDEN FOR ACCREDITATION BODIES—Continued Number of respondents 42 CFR citation Purpose 8.3(c) .................... 8.3(e) .................... 8.3(f)(2) ................ Renewal of approval (SMA–163) ...... Relinquishment notification ................ Non-renewal notification to accredited OTPs. Notification to SAMHSA for seriously noncompliant OTPs. Notification to OTP for serious noncompliance. General documents and information to SAMHSA upon request. Accreditation survey to SAMHSA upon request. List of surveys, surveyors to SAMHSA upon request. Report of less than full accreditation to SAMHSA. Summaries of Inspections ................. Notifications of Complaints ................ Revocation notification to Accredited OTPs. Submission of 90-day corrective plan to SAMHSA. Notification to accredited OTPs of Probationary Status. 8.4(b)(1)(ii) ........... 8.4(b)(1)(iii) .......... 8.4(d)(1) ............... 8.4(d)(2) ............... 8.4(d)(3) ............... 8.4(d)(4) ............... 8.4(d)(5) ............... 8.4(e) .................... 8.6(a)(2) and (b)(3). 8.6(b) .................... 8.6(b)(1) ............... Sub Total ...... Responses/ respondent Total responses Hours/ response Total hours 2 1 1 2 1 90 1.00 0.50 0.10 2.00 0.50 9.00 2 2 4 1.00 4.00 2 10 20 1.00 20.00 6 5 30 0.50 15.00 6 75 450 0.02 9.00 6 6 36 0.20 7.20 6 5 30 0.50 15.00 6 12 1 50 6 185 300 72 185 0.50 0.50 0.30 150.00 36.00 55.50 1 1 1 10.00 10.00 1 185 185 0.30 55.50 54 ............................................................ 1 1 90 ........................ 1,407 ........................ 394.70 ESTIMATED ANNUAL REPORTING REQUIREMENT BURDEN FOR OPIOID TREATMENT PROGRAMS Number of respondents 42 CFR citation Purpose 8.11(b) .................. 8.11(b) .................. 8.11(e)(1) ............. Renewal of approval (SMA–162) ...... Relocation of Program (SMA–162) ... Application for provisional certification. Application for extension of provisional certification. Notification of sponsor or medical director change (SMA–162). Documentation to SAMHSA for interim maintenance. Request to SAMHSA for Exemption from 8.11 and 8.12 (including SMA–168). Notification to SAMHSA Before Establishing Medication Units (SMA– 162). Notification to State Health Officer When Patient Begins Interim Maintenance. Contents of Appellant Request for Review of Suspension. Informal Review Request .................. Appellant’s Review File and Written Statement. Appellant’s Request for Expedited Review. Appellant Review File and Written Statement. 8.11(e)(2) ............. 8.11(f)(5) .............. 8.11(g)(2) ............. 8.11(h) .................. 8.11(i)(1) .............. 8.12(j)(2) .............. 8.24 ...................... 8.25(a) .................. 8.26(a) .................. 8.28(a) .................. mstockstill on DSK4VPTVN1PROD with NOTICES 8.28(c) .................. Responses/ respondent Total responses Hours/ response Total hours 386 35 42 1 1 1 386 35 42 0.15 1.17 1.00 57.90 40.95 42.00 30 1 30 0.25 7.50 60 1 60 0.10 6.00 1 1 1 1.00 1.00 1,325 25 33,125 0.07 2,318.75 10 1 10 0.25 2.50 1 20 20 0.33 6.60 2 1 2 0.25 .50 2 2 1 1 2 2 1.00 5.00 2.00 10.00 2 1 2 1.00 2.00 2 1 2 5.00 10.00 Sub Total ...... ............................................................ 1,900 ........................ 33,719 ........................ 2,507.70 Total ....... ............................................................ 1,954 ........................ 35,126 ........................ 2,902.40 VerDate Sep<11>2014 18:02 Apr 18, 2016 Jkt 238001 PO 00000 Frm 00037 Fmt 4703 Sfmt 4703 E:\FR\FM\19APN1.SGM 19APN1 Federal Register / Vol. 81, No. 75 / Tuesday, April 19, 2016 / Notices Send comments to Summer King, SAMHSA Reports Clearance Officer, 5600 Fishers Lane, Room 15E57B, Rockville, MD 20857 or email a copy at summer.king@samhsa.hhs.gov. Written comments should be received by June 20, 2016. Summer King, Statistician. [FR Doc. 2016–09020 Filed 4–18–16; 8:45 am] DEPARTMENT OF HOMELAND SECURITY Coast Guard [Docket No. USCG–2016–0291] Cooperative Research and Development Agreement: Troposcatter Communications Exploratory Development Coast Guard, DHS. Notice of intent; request for comments. AGENCY: BILLING CODE 4162–20–P ACTION: The Coast Guard announces its intent to enter into a Cooperative Research and Development Agreement (CRADA) with Comtech Systems, Inc., Coast Guard to investigate the potential operational use of troposcatter technology. The [Docket No. USCG–2016–0104] research includes employment of their Modular Transportable Transmission Navigation and Vessel Inspection System (MTTS) in northern Alaska to Circular (NVIC) No. 02–16; Inspection establish beyond line of sight (BLOS) Guidance for Sail Rigging and Masts network links without using existing on Inspected Sailing Vessels infrastructure or satellite communications. Specifically, the AGENCY: Coast Guard, DHS. MTTS will provide a wireless IEEE ACTION: Notice of availability. 802.3 (Ethernet) data link between two locations separated by long distances SUMMARY: The Coast Guard announces and elevated terrain. The MTTS will be the availability of NVIC 02–16. This setup in locations with no shelter/ Circular provides guidance to vessel owners, riggers, marine surveyors, other protection from the Northern Alaskan environment. A Pilot Demonstration marine service providers, and Coast schedule has been proposed in which Guard marine inspectors regarding Comtech Systems will provide their inspection of sail rigging, masts, and MTTS to connect two points separated associated components for commercial by 68 miles with a 3000 foot elevation sailing vessels and the use of in between. The Coast Guard Research preventative maintenance as a good and Development Center (R&D Center) marine practice. It provides guidance for will prepare a Pilot Demonstration the purpose of assisting vessel owners Assessment Plan and Comtech Systems and operators, and U.S. Coast Guard will operate the equipment for personnel with the inspection and exploratory development over a one recommended documentation of week period to collect information on maintenance for sail rigging and masts suitability, reliability, maintenance on inspected sailing vessels. It is requirements, and ease of use. While the intended to enhance consistency with Coast Guard is currently considering the Coast Guard inspection process for partnering with Comtech Systems, Inc., the commercial sailing fleet. the agency is soliciting public comment DATES: NVIC 02–16 is available on April on the possible nature of and 13, 2016. participation of other parties in the ADDRESSES: This NVIC is available at the proposed CRADA. In addition, the Coast Guard also invites other potential nonfollowing Coast Guard Web site: https:// Federal participants to propose similar www.uscg.mil/hq/cg5/nvic/. CRADAs. FOR FURTHER INFORMATION CONTACT: If DATES: Comments must be submitted to you have questions on this notice, call the online docket via https:// LCDR James T. Fogle, Office of www.regulations.gov, or reach the Commercial Vessel Compliance, Coast Guard, telephone 202—372–1216, email Docket Management Facility, on or before May 19, 2016. James.T.Fogle@uscg.mil. Synopses of proposals regarding Dated: April 13, 2016. future CRADAs must reach the Coast Paul F. Thomas, Guard (see FOR FURTHER INFORMATION USCG, Assistant Commandant for Prevention CONTACT) on or before May 19, 2016. Policy. ADDRESSES: Submit comments online at [FR Doc. 2016–09022 Filed 4–18–16; 8:45 am] https://www.regulations.gov in accordance with Web site instructions. BILLING CODE 9110–04–P mstockstill on DSK4VPTVN1PROD with NOTICES DEPARTMENT OF HOMELAND SECURITY VerDate Sep<11>2014 18:02 Apr 18, 2016 Jkt 238001 SUMMARY: PO 00000 Frm 00038 Fmt 4703 Sfmt 4703 23001 If you have questions on this notice or wish to submit proposals for future CRADAs, contact LCDR Samuel Nassar, Project Official, C4ISR Branch, U.S. Coast Guard Research and Development Center, 1 Chelsea Street, New London, CT 06320, telephone 860–271–2727, email samuel.r.nassar@uscg.mil. SUPPLEMENTARY INFORMATION: FOR FURTHER INFORMATION CONTACT: Public Participation and Request for Comments We request public comments on this notice. Although we do not plan to respond to comments in the Federal Register, we will respond directly to commenters and may modify our proposal in light of comments. Comments should be marked with docket number USCG–2016–0291and should provide a reason for each suggestion or recommendation. You should provide personal contact information so that we can contact you if we have questions regarding your comments; but please note that all comments will be posted to the online docket without change and that any personal information you include can be searchable online (see the Federal Register Privacy Act notice regarding our public dockets, 73 FR 3316, Jan. 17, 2008). We also accept anonymous comments. We encourage you to submit comments through the Federal eRulemaking Portal at https:// www.regulations.gov. If your material cannot be submitted using https:// www.regulations.gov, contact the Coast Guard (see FOR FURTHER INFORMATION CONTACT). Documents mentioned in this notice and all public comments, are in our online docket at https:// www.regulations.gov and can be viewed by following that Web site’s instructions. Additionally, if you go to the online docket and sign up for email alerts, you will be notified when comments are posted or a final rule is published. Do not submit detailed proposals for future CRADAs to the Docket Management Facility. Instead, submit them directly to the Coast Guard (see FOR FURTHER INFORMATION CONTACT). Discussion CRADAs are authorized under 15 U.S.C. 3710(a).1 A CRADA promotes the transfer of technology to the private sector for commercial use, as well as specified research or development 1 The statute confers this authority on the head of each Federal agency. The Secretary of DHS’s authority is delegated to the Coast Guard and other DHS organizational elements by DHS Delegation No. 0160.1, para. II.B.34. E:\FR\FM\19APN1.SGM 19APN1

Agencies

[Federal Register Volume 81, Number 75 (Tuesday, April 19, 2016)]
[Notices]
[Pages 22999-23001]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-09020]


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

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 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 on (240) 276-1243.
    Comments are invited on: (a) Whether the proposed collections of 
information 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: Opioid Drugs in Maintenance and Detoxification 
Treatment of Opioid Dependence--42 CFR part 8 (OMB No. 0930-0206) and 
Opioid Treatment Programs (OTPs)--Revision

    42 CFR part 8 establishes a certification program managed by 
SAMHSA's Center for Substance Abuse Treatment (CSAT). The regulation 
requires that Opioid Treatment Programs (OTPs) be certified. 
``Certification'' is the process by which SAMHSA determines that an OTP 
is qualified to provide opioid treatment under the Federal opioid 
treatment standards established by the Secretary of Health and Human 
Services. To become certified, an OTP must be accredited by a SAMHSA-
approved accreditation body. The regulation also provides standards for 
such services as individualized treatment planning, increased medical 
supervision, and assessment of patient outcomes. This submission seeks 
continued approval of the information collection requirements in the 
regulation and of the forms used in implementing the regulation.
    SAMHSA currently has approval for the Application for Certification 
to Use Opioid Drugs in a Treatment Program Under 42 CFR 8.11 (Form SMA-
162); the Application for Approval as Accreditation Body Under 42 CFR 
8.3(b) (Form SMA-163); and the Exception Request and Record of 
Justification Under 42 CFR 8.12 (Form SMA-168), which may be used by 
physicians when there is a patient care situation in which the 
physician must make a treatment decision that differs from the 
treatment regimen required by the regulation. Form SMA-168 is a 
simplified, standardized form to facilitate the documentation, request, 
and approval process for exceptions.
    SAMHSA believes that the recordkeeping requirements in the 
regulation are customary and usual practices within the medical and 
rehabilitative communities and has not calculated a response burden for 
them. The recordkeeping requirements set forth in 42 CFR 8.4, 8.11, and 
8.12 include maintenance of the following: 5-year retention by 
accreditation bodies of certain records pertaining to accreditation, 
and documentation by an OTP of the following: A patient's medical 
examination when admitted to treatment, a patient's history, a 
treatment plan, any prenatal support provided to the patient, 
justification of unusually large initial doses, changes in a patient's 
dosage schedule, justification of unusually large daily doses, the 
rationale for decreasing a patient's clinic attendance, and 
documentation of physiologic dependence.
    The rule also includes requirements that OTPs and accreditation 
organizations disclose information. For example, 42 CFR 8.12(e)(1) 
requires that a physician explain the facts concerning the use of 
opioid drug treatment to each patient. This type of disclosure is 
considered to be consistent with the common medical practice and is not 
considered an additional burden. Further, the rule requires, under Sec. 
8.4(i)(1) that accreditation organizations shall make public their fee 
structure; this type of disclosure is standard business practice and is 
not considered a burden.
    A number of changes have been made to the forms. Forms have been 
reworded for clarification, updated with current SAMHSA mailing and 
web-submission information, and a few additional fields have been 
provided for clarity and for providers to best explain their services 
(e.g., expanding the former global patient census in the SMA-162 to 
request patient census by drug type--methadone, buprenorphine, 
naltrexone, or other) and the needs of their patients (e.g., including 
urinalysis results on the SMA-168 and adding ``weather crisis'' as a 
standard option for physician justification of the requested 
exception). Amendments also include the removal of information 
pertaining to faxing the forms to SAMHSA, as this is no longer an 
acceptable form of submission. The burden hours have increased slightly 
(by 28% or approximately 639 hours) due to an increase in the number of 
facilities accredited and certified by SAMHSA since the previous 
submissions of these forms. The forms are available online with a 
unique feature for both the SMA-162 and SMA-168 that pre-populates 
certain information within the form. This in turn reduces the program's 
time spent filling out the forms as well as the staff time spent on 
processing it.
    The tables that follow summarize the annual reporting burden 
associated with the regulation, including burden associated with the 
forms.

                                         Estimated Annual Reporting Requirement Burden for Accreditation Bodies
--------------------------------------------------------------------------------------------------------------------------------------------------------
                                                                             Number of      Responses/         Total          Hours/
            42 CFR citation                          Purpose                respondents     respondent       responses       response       Total hours
--------------------------------------------------------------------------------------------------------------------------------------------------------
8.3(b)(1-11)...........................  Initial approval (SMA-163).....               1               1               1            6.00            6.00

[[Page 23000]]

 
8.3(c).................................  Renewal of approval (SMA-163)..               2               1               2            1.00            2.00
8.3(e).................................  Relinquishment notification....               1               1               1            0.50            0.50
8.3(f)(2)..............................  Non-renewal notification to                   1              90              90            0.10            9.00
                                          accredited OTPs.
8.4(b)(1)(ii)..........................  Notification to SAMHSA for                    2               2               4            1.00            4.00
                                          seriously noncompliant OTPs.
8.4(b)(1)(iii).........................  Notification to OTP for serious               2              10              20            1.00           20.00
                                          noncompliance.
8.4(d)(1)..............................  General documents and                         6               5              30            0.50           15.00
                                          information to SAMHSA upon
                                          request.
8.4(d)(2)..............................  Accreditation survey to SAMHSA                6              75             450            0.02            9.00
                                          upon request.
8.4(d)(3)..............................  List of surveys, surveyors to                 6               6              36            0.20            7.20
                                          SAMHSA upon request.
8.4(d)(4)..............................  Report of less than full                      6               5              30            0.50           15.00
                                          accreditation to SAMHSA.
8.4(d)(5)..............................  Summaries of Inspections.......               6              50             300            0.50          150.00
8.4(e).................................  Notifications of Complaints....              12               6              72            0.50           36.00
8.6(a)(2) and (b)(3)...................  Revocation notification to                    1             185             185            0.30           55.50
                                          Accredited OTPs.
8.6(b).................................  Submission of 90-day corrective               1               1               1           10.00           10.00
                                          plan to SAMHSA.
8.6(b)(1)..............................  Notification to accredited OTPs               1             185             185            0.30           55.50
                                          of Probationary Status.
                                                                         -------------------------------------------------------------------------------
    Sub Total..........................  ...............................              54  ..............           1,407  ..............          394.70
--------------------------------------------------------------------------------------------------------------------------------------------------------


                                       Estimated Annual Reporting Requirement Burden for Opioid Treatment Programs
--------------------------------------------------------------------------------------------------------------------------------------------------------
                                                                             Number of      Responses/         Total          Hours/
            42 CFR citation                          Purpose                respondents     respondent       responses       response       Total hours
--------------------------------------------------------------------------------------------------------------------------------------------------------
8.11(b)................................  Renewal of approval (SMA-162)..             386               1             386            0.15           57.90
8.11(b)................................  Relocation of Program (SMA-162)              35               1              35            1.17           40.95
8.11(e)(1).............................  Application for provisional                  42               1              42            1.00           42.00
                                          certification.
8.11(e)(2).............................  Application for extension of                 30               1              30            0.25            7.50
                                          provisional certification.
8.11(f)(5).............................  Notification of sponsor or                   60               1              60            0.10            6.00
                                          medical director change (SMA-
                                          162).
8.11(g)(2).............................  Documentation to SAMHSA for                   1               1               1            1.00            1.00
                                          interim maintenance.
8.11(h)................................  Request to SAMHSA for Exemption           1,325              25          33,125            0.07        2,318.75
                                          from 8.11 and 8.12 (including
                                          SMA-168).
8.11(i)(1).............................  Notification to SAMHSA Before                10               1              10            0.25            2.50
                                          Establishing Medication Units
                                          (SMA-162).
8.12(j)(2).............................  Notification to State Health                  1              20              20            0.33            6.60
                                          Officer When Patient Begins
                                          Interim Maintenance.
8.24...................................  Contents of Appellant Request                 2               1               2            0.25             .50
                                          for Review of Suspension.
8.25(a)................................  Informal Review Request........               2               1               2            1.00            2.00
8.26(a)................................  Appellant's Review File and                   2               1               2            5.00           10.00
                                          Written Statement.
8.28(a)................................  Appellant's Request for                       2               1               2            1.00            2.00
                                          Expedited Review.
8.28(c)................................  Appellant Review File and                     2               1               2            5.00           10.00
                                          Written Statement.
                                                                         -------------------------------------------------------------------------------
    Sub Total..........................  ...............................           1,900  ..............          33,719  ..............        2,507.70
                                                                         -------------------------------------------------------------------------------
        Total..........................  ...............................           1,954  ..............          35,126  ..............        2,902.40
--------------------------------------------------------------------------------------------------------------------------------------------------------


[[Page 23001]]

    Send comments to Summer King, SAMHSA Reports Clearance Officer, 
5600 Fishers Lane, Room 15E57B, Rockville, MD 20857 or email a copy at 
summer.king@samhsa.hhs.gov. Written comments should be received by June 
20, 2016.

Summer King,
Statistician.
[FR Doc. 2016-09020 Filed 4-18-16; 8:45 am]
 BILLING CODE 4162-20-P