Agency Information Collection Activities: Proposed Collection; Comment Request, 3013-3015 [2013-00585]

Download as PDF Federal Register / Vol. 78, No. 10 / Tuesday, January 15, 2013 / Notices and Hematology Research, National Institutes of Health, HHS) DEPARTMENT OF HEALTH AND HUMAN SERVICES Dated: January 8, 2013. David Clary, Program Analyst, Office of Federal Advisory Committee Policy. Substance Abuse and Mental Health Services Administration [FR Doc. 2013–00620 Filed 1–14–13; 8:45 am] BILLING CODE 4140–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES National Institutes of Health Center for Scientific Review; 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 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. srobinson on DSK4SPTVN1PROD with Name of Committee: Center for Scientific Review Special Emphasis Panel; Member Conflict: Neurodevelopment and Neuroplasticity. Date: January 28, 2013. Time: 1:00 p.m. to 2:30 p.m. Agenda: To review and evaluate grant applications. Place: National Institutes of Health, 6701 Rockledge Drive, Bethesda, MD 20892, (Telephone Conference Call). Contact Person: Toby Behar, Ph.D., Scientific Review Officer, Center for Scientific Review, National Institutes of Health, 6701 Rockledge Drive, Room 4136, MSC 7850, Bethesda, MD 20892, (301) 435– 4433, behart@csr.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 Nos. 93.306, Comparative Medicine; 93.333, Clinical Research, 93.306, 93.333, 93.337, 93.393–93.396, 93.837–93.844, 93.846–93.878, 93.892, 93.893, National Institutes of Health, HHS) Dated: January 9, 2013. David Clary, Program Analyst, Office of Federal Advisory Committee Policy. [FR Doc. 2013–00615 Filed 1–14–13; 8:45 am] BILLING CODE 4140–01–P VerDate Mar<15>2010 17:00 Jan 14, 2013 Jkt 229001 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 PO 00000 Frm 00075 Fmt 4703 Sfmt 4703 3013 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 on a voluntary basis 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; 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 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. There are no changes being made to the forms. The reason for the reduction in burden hours is due to more respondents submitting information through an online function. 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 E:\FR\FM\15JAN1.SGM 15JAN1 3014 Federal Register / Vol. 78, No. 10 / Tuesday, January 15, 2013 / Notices filling out the forms as well as the staff time spent on processing it. Also, a final rule effective January 7, 2013, (77 FR 72752, Federal Register December 6, 2012) eliminated dispensing restrictions for buprenorphine products used in OTPs. As a result there OTPs will complete and submit fewer SMA–168 forms, therefore reducing burden hours. 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) .................................... 8.3(c) ............................................... 8.3(e) ............................................... 8.3(f)(2) ........................................... Initial approval (SMA–163) ............. 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 ................................. 54 .................................................... Responses/ respondent Total responses Hours/ response Total hours 1 2 1 1 1 1 1 90 1 2 1 90 6.0 1.0 0.5 0.1 6 2 0.5 9 2 2 4 1.0 4 2 10 20 1.0 20 6 5 30 0.5 15 6 75 450 0.02 9 6 6 36 0.2 7.2 6 5 30 0.5 15 6 12 1 50 6 185 300 72 185 0.5 0.5 0.3 150 36 55.5 1 1 1 10 10.0 1 185 185 0.3 55.0 ........................ 1,407 .................... 394.20 ESTIMATED ANNUAL REPORTING REQUIREMENT BURDEN FOR OPIOID TREATMENT PROGRAMS Number of espondents 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 ................................................. srobinson on DSK4SPTVN1PROD with 8.25(a) ............................................. 8.26(a) ............................................. 8.28(a) ............................................. 8.28(c) ............................................. Sub Total ................................. VerDate Mar<15>2010 17:00 Jan 14, 2013 PO 00000 Frm 00076 Fmt 4703 Total responses Hours/ response Total hours 386 35 42 386 35 42 0.15 1.17 1 57.9 40.95 42.00 1 30 0.25 7.50 60 1 60 0.1 6.00 1 1 1 1 1.00 1,200 20 24,000 0.07 1680 10 1 10 0.25 2.5 1 20 20 0.33 6.6 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 1,775 Sfmt 4703 1 1 1 30 ......................................................... Jkt 229001 Responses/ respondent .................... 24,594 ................ 1868.95 E:\FR\FM\15JAN1.SGM 15JAN1 3015 Federal Register / Vol. 78, No. 10 / Tuesday, January 15, 2013 / Notices ESTIMATED ANNUAL REPORTING REQUIREMENT BURDEN FOR OPIOID TREATMENT PROGRAMS—Continued 42 CFR citation Number of espondents Purpose Total .................................. ......................................................... Send comments to Summer King, SAMHSA Reports Clearance Officer, Room 2–1057, One Choke Cherry Road, Rockville, MD 20857 or email her a copy at summer.king@samhsa.hhs.gov. Written comments should be received by March 18, 2013. Summer King, Statistician. [FR Doc. 2013–00585 Filed 1–14–13; 8:45 am] BILLING CODE 4162–20–P DEPARTMENT OF HOMELAND SECURITY Office of the Secretary [Docket No. DHS–2012–0034] 1,829 Responses/ respondent .................... • Federal e-Rulemaking Portal: http://www.regulations.gov. Follow the instructions for submitting comments. • Fax: 202–343–4010. • Mail: Jonathan R. Cantor, Acting Chief Privacy Officer, Privacy Office, Department of Homeland Security, Washington, DC 20528. Instructions: All submissions received must include the agency name and docket number for this rulemaking. All comments received will be posted without change to http:// www.regulations.gov, including any personal information provided. Docket: For access to the docket to read background documents or comments received, visit http:// www.regulations.gov. For general questions, please contact: Laurence E. Castelli, 202–325–0280, CBP Privacy Officer, Office of International Trade/Regulations and Rulings, U.S. Customs and Border Protection, Mint Annex, 799 9th Street NW., Washington, DC 20229–1177. For privacy issues, please contact: Jonathan R. Cantor, 202–343–1717, Acting Chief Privacy Officer, Privacy Office, Department of Homeland Security, Washington, DC 20528. SUPPLEMENTARY INFORMATION: FOR FURTHER INFORMATION CONTACT: Privacy Act of 1974; U.S. Customs and Border Protection; DHS/CBP–004– Intellectual Property Rights eRecordation and Search Systems, System of Records Department of Homeland Security, Privacy Office. ACTION: Notice of Privacy Act system of records. AGENCY: In accordance with the Privacy Act of 1974, the Department of Homeland Security, U.S. Customs and Border Protection proposes to establish a new system of records titled, ‘‘U.S. Customs and Border Protection, DHS/ CBP–004–Intellectual Property Rights eRecordation and Search Systems System of Records.’’ This system of records allows the Department and CBP to collect and maintain records on copyrights, trademarks, and trade names that the respective owners have applied to have recorded with CBP. In addition, the Department is issuing a Notice of Proposed Rulemaking elsewhere in the Federal Register to exempt this system of records from certain provisions of the Privacy Act. This newly established system will be included in the Department’s inventory of record systems. SUMMARY: Submit comments on or before February 14, 2013. This new system will be effective February 14, 2013. ADDRESSES: You may submit comments, identified by docket number DHS– 2012–034 by one of the following methods: srobinson on DSK4SPTVN1PROD with DATES: VerDate Mar<15>2010 17:00 Jan 14, 2013 Jkt 229001 I. Background In accordance with the Privacy Act of 1974, 5 U.S.C. 552a, the Department of Homeland Security (DHS), U.S. Customs and Border Protection (CBP) proposes to establish a new DHS system of records titled, ‘‘DHS/CBP–004–Intellectual Property Rights e-Recordation and Search Systems System of Records.’’ The Intellectual Property Rights eRecordation and Search Systems (IPRRSS) collect, use, and maintain records related to intellectual property rights recordations and their owners. The purpose of IPRRSS is to aid in the enforcement of intellectual property rights by making intellectual property recordations available to the public and to CBP officials. IPRRSS collectively encompasses three separate systems. The first system is the online Intellectual Property Rights e-Recordation (IPRR) system, which allows intellectual property owners to submit applications for trademark and copyright recordations. The IPRR PO 00000 Frm 00077 Fmt 4703 Sfmt 4703 Total responses 26,001 Hours/ response Total hours ................ 2,263.15 system shares information with the public Intellectual Property Rights Search (IPRS) system and the CBP Intellectual Property Rights Internal Search (IPRiS) system. Because CBP may collect personally identifiable information (PII) about intellectual property rights holders, their agents, or their licensees in IPRR, IPRS, and IPRiS (collectively IPRRSS), CBP is providing the public notice about how CBP collects, uses, and maintains records related to intellectual property rights recordations. The authority for this system derives from Section 42 of the Lanham Act (Trademark Act of 1946), as amended, 15 U.S.C. 1124; Sections 101 and 602 through 603 of the Copyright Act of 1976, as amended, 17 U.S.C. 101, 602– 603; and Sections 526, 595a, and 624 of the Tariff Act of 1930, as amended, 19 U.S.C. 1526, 1595a, and 1624. The cited sections provide that intellectual property rights owners may submit information to CBP to enable CBP officials to identify infringing articles at the borders and prevent the importation of counterfeit or pirated merchandise. Owners seeking to have merchandise excluded from entry must provide proof to CBP of the validity of the intellectual property rights they seek to protect. Pursuant to the Independent Offices Appropriations Act of 1952, 31 U.S.C. 9701, and regulations at 19 CFR 133.3, 133.13, and 133.33, intellectual property rights owners or their agents must pay a fee when they apply for the recordation with CBP of their trademark, trade name, or copyright. Through IPRR’s web-based interface, the user will be prompted through several steps that capture the user’s required application information. Once the applicant has entered all required application information, IPRR will guide the applicant through a series of prompts seeking his/her billing name, billing address, and credit card information. IPRR forwards this payment information to Pay.gov for payment processing, and the applicant name and an IPRR tracking number to the DHS/CBP–003 Credit/Debit Card Data System (CDCDS) System of Records for payment reconciliation. Pay.gov sends a nightly activity file, including the last four digits of the credit card, authorization number, billing name, billing address, IPRR E:\FR\FM\15JAN1.SGM 15JAN1

Agencies

[Federal Register Volume 78, Number 10 (Tuesday, January 15, 2013)]
[Notices]
[Pages 3013-3015]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2013-00585]


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

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 on a 
voluntary basis 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; 
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 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.
    There are no changes being made to the forms. The reason for the 
reduction in burden hours is due to more respondents submitting 
information through an online function. 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

[[Page 3014]]

filling out the forms as well as the staff time spent on processing it. 
Also, a final rule effective January 7, 2013, (77 FR 72752, Federal 
Register December 6, 2012) eliminated dispensing restrictions for 
buprenorphine products used in OTPs. As a result there OTPs will 
complete and submit fewer SMA-168 forms, therefore reducing burden 
hours.
    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/     Total
        42 CFR citation              Purpose        respondents    respondent   responses    response    hours
----------------------------------------------------------------------------------------------------------------
8.3(b)(1-11)..................  Initial approval               1            1            1        6.0          6
                                 (SMA-163).
8.3(c)........................  Renewal of                     2            1            2        1.0          2
                                 approval (SMA-
                                 163).
8.3(e)........................  Relinquishment                 1            1            1        0.5        0.5
                                 notification.
8.3(f)(2).....................  Non-renewal                    1           90           90        0.1          9
                                 notification to
                                 accredited OTPs.
8.4(b)(1)(ii).................  Notification to                2            2            4        1.0          4
                                 SAMHSA for
                                 seriously
                                 noncompliant
                                 OTPs.
8.4(b)(1)(iii)................  Notification to                2           10           20        1.0         20
                                 OTP for serious
                                 noncompliance.
8.4(d)(1).....................  General                        6            5           30        0.5         15
                                 documents and
                                 information to
                                 SAMHSA upon
                                 request.
8.4(d)(2).....................  Accreditation                  6           75          450       0.02          9
                                 survey to
                                 SAMHSA upon
                                 request.
8.4(d)(3).....................  List of surveys,               6            6           36        0.2        7.2
                                 surveyors to
                                 SAMHSA upon
                                 request.
8.4(d)(4).....................  Report of less                 6            5           30        0.5         15
                                 than full
                                 accreditation
                                 to SAMHSA.
8.4(d)(5).....................  Summaries of                   6           50          300        0.5        150
                                 Inspections.
8.4(e)........................  Notifications of              12            6           72        0.5         36
                                 Complaints.
8.6(a)(2) and (b)(3)..........  Revocation                     1          185          185        0.3       55.5
                                 notification to
                                 Accredited OTPs.
8.6(b)........................  Submission of 90-              1            1            1         10       10.0
                                 day corrective
                                 plan to SAMHSA.
8.6(b)(1).....................  Notification to                1          185          185        0.3       55.0
                                 accredited OTPs
                                 of Probationary
                                 Status.
                               ---------------------------------------------------------------------------------
    Sub Total.................  54..............  ..............        1,407  ...........     394.20
----------------------------------------------------------------------------------------------------------------


                   Estimated Annual Reporting Requirement Burden for Opioid Treatment Programs
----------------------------------------------------------------------------------------------------------------
                                                     Number of     Responses/     Total       Hours/     Total
        42 CFR citation              Purpose        respondents    respondent   responses    response    hours
----------------------------------------------------------------------------------------------------------------
8.11(b).......................  Renewal of                   386            1          386       0.15       57.9
                                 approval (SMA-
                                 162).
8.11(b).......................  Relocation of                 35            1           35       1.17      40.95
                                 Program (SMA-
                                 162).
8.11(e)(1)....................  Application for               42            1           42          1      42.00
                                 provisional
                                 certification.
8.11(e)(2)....................  Application for               30            1           30       0.25       7.50
                                 extension of
                                 provisional
                                 certification.
8.11(f)(5)....................  Notification of               60            1           60        0.1       6.00
                                 sponsor or
                                 medical
                                 director change
                                 (SMA-162).
8.11(g)(2)....................  Documentation to               1            1            1          1       1.00
                                 SAMHSA for
                                 interim
                                 maintenance.
8.11(h).......................  Request to                 1,200           20       24,000       0.07       1680
                                 SAMHSA for
                                 Exemption from
                                 8.11 and 8.12
                                 (including SMA-
                                 168).
8.11(i)(1)....................  Notification to               10            1           10       0.25        2.5
                                 SAMHSA Before
                                 Establishing
                                 Medication
                                 Units (SMA-162).
8.12(j)(2)....................  Notification to                1           20           20       0.33        6.6
                                 State Health
                                 Officer When
                                 Patient Begins
                                 Interim
                                 Maintenance.
8.24..........................  Contents of                    2            1            2       0.25        .50
                                 Appellant
                                 Request for
                                 Review of
                                 Suspension.
8.25(a).......................  Informal Review                2            1            2       1.00       2.00
                                 Request.
8.26(a).......................  Appellant's                    2            1            2       5.00      10.00
                                 Review File and
                                 Written
                                 Statement.
8.28(a).......................  Appellant's                    2            1            2       1.00       2.00
                                 Request for
                                 Expedited
                                 Review.
8.28(c).......................  Appellant Review               2            1            2       5.00      10.00
                                 File and
                                 Written
                                 Statement.
                               ---------------------------------------------------------------------------------
    Sub Total.................  ................           1,775  ...........       24,594  .........    1868.95
                               ---------------------------------------------------------------------------------

[[Page 3015]]

 
        Total.................  ................           1,829  ...........       26,001  .........   2,263.15
----------------------------------------------------------------------------------------------------------------

    Send comments to Summer King, SAMHSA Reports Clearance Officer, 
Room 2-1057, One Choke Cherry Road, Rockville, MD 20857 or email her a 
copy at summer.king@samhsa.hhs.gov. Written comments should be received 
by March 18, 2013.

Summer King,
Statistician.
[FR Doc. 2013-00585 Filed 1-14-13; 8:45 am]
BILLING CODE 4162-20-P