Agency Information Collection Activities: Submission for OMB Review; Comment Request, 66211-66213 [2019-26001]

Download as PDF Federal Register / Vol. 84, No. 232 / Tuesday, December 3, 2019 / Notices DEPARTMENT OF HEALTH AND HUMAN SERVICES National Institutes of Health National Institute of Biomedical Imaging and Bioengineering; Notice of Closed Meeting Pursuant to section 10(d) of the Federal Advisory Committee Act, as amended, 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: National Institute of Biomedical Imaging and Bioengineering Special Emphasis Panel; BRAIN Initiative: Theories, Models and Methods for Analysis of Complex Data from the Brain (2020/05). Date: February 13, 2020. Time: 9:00 a.m. to 7:00 p.m. Agenda: To review and evaluate grant applications. Place: National Institutes of Health, Two Democracy Plaza, 6707 Democracy Boulevard Bethesda, MD 20892 (Virtual Meeting). Contact Person: Dennis Hlasta, Ph.D., Scientific Review Officer, National Institute of Biomedical Imaging and Bioengineering, National Institutes of Health, 6707 Democracy Blvd., Bethesda, MD 20892, (301) 451–4794, dennis.hlasta@nih.gov. Dated: November 26, 2019. Miguelina Perez, Program Analyst, Office of Federal Advisory Committee Policy. [FR Doc. 2019–26063 Filed 12–2–19; 8:45 am] BILLING CODE 4140–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES National Institutes of Health lotter on DSKBCFDHB2PROD with NOTICES National Institute on Deafness and Other Communication Disorders; Notice of Meetings Pursuant to section 10(d) of the Federal Advisory Committee Act, as amended, notice is hereby given of meetings of the National Deafness and Other Communication Disorders Advisory Council. The meetings will be open to the public as indicated below, with attendance limited to space available. Individuals who plan to attend and VerDate Sep<11>2014 18:27 Dec 02, 2019 Jkt 250001 need special assistance, such as sign language interpretation or other reasonable accommodations, should notify the Contact Person listed below in advance of the meeting. The meetings 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: National Deafness and Other Communication Disorders Advisory Council. Date: January 31, 2020. Closed: 8:30 a.m. to 10:00 a.m. Agenda: To review and evaluate grant applications. Place: National Institutes of Health, Neuroscience Center Building (NSC), Room C and D, 6001 Executive Boulevard, Rockville, MD 20852. Open: 10:00 a.m. to 2:00 p.m. Agenda: Staff reports on divisional, programmatical, and special activities. Place: National Institutes of Health, Neuroscience Center Building (NSC), Room C and D, 6001 Executive Boulevard, Rockville, MD 20852. Contact Person: Craig A. Jordan, Ph.D., Director, Division of Extramural Activities, NIDCD, NIH, Room 8345, MSC 9670, 6001 Executive Blvd., Bethesda, MD 20892–9670, 301–496–8693, jordanc@nidcd.nih.gov. Name of Committee: National Deafness and Other Communication Disorders Advisory Council. Date: May 29, 2020. Closed: 8:30 a.m. to 10:00 a.m. Agenda: To review and evaluate grant applications. Place: Porter Neuroscience Research Center, Building 35A, Room 620, 35 Convent Drive, Bethesda, MD 20892. Open: 10:00 a.m. to 2:00 p.m. Agenda: staff reports on divisional, programmatical, and special activities. Place: Porter Neuroscience Research Center, Building 35A, Room 620, 35 Convent Drive, Bethesda, MD 20892. Contact Person: Craig A. Jordan, Ph.D., Director, Division of Extramural Activities, NIDCD, NIH, Room 8345, MSC 9670, 6001 Executive Blvd., Bethesda, MD 20892–9670, 301–496–8693, jordanc@nidcd.nih.gov. Any interested person may file written comments with the committee by forwarding the statement to the Contact Person listed on this notice. The statement should include the name, address, telephone number and when applicable, the business or professional affiliation of the interested person. In the interest of security, NIH has instituted stringent procedures for entrance onto the NIH campus. All visitor vehicles, including taxicabs, hotel, and airport shuttles PO 00000 Frm 00066 Fmt 4703 Sfmt 4703 66211 will be inspected before being allowed on campus. Visitors will be asked to show one form of identification (for example, a government-issued photo ID, driver’s license, or passport) and to state the purpose of their visit. Information is also available on the Institute’s/Center’s home page: https:// www.nidcd.nih.gov/about/advisory-council, where an agenda and any additional information for the meeting will be posted when available. (Catalogue of Federal Domestic Assistance Program Nos. 93.173, Biological Research Related to Deafness and Communicative Disorders, National Institutes of Health, HHS) Dated: November 26, 2019. Sylvia L. Neal, Program Analyst, Office of Federal Advisory Committee Policy. [FR Doc. 2019–26065 Filed 12–2–19; 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: Submission for OMB Review; Comment Request Periodically, the Substance Abuse and Mental Health Services Administration (SAMHSA) will publish a summary of information collection requests under OMB review, in compliance with the Paperwork Reduction Act (44 U.S.C. chapter 35). To request a copy of these documents, call the SAMHSA Reports Clearance Officer on (240) 276–1243. Project: Notification of Intent To Use Schedule III, IV, or V Opioid Drugs for the Maintenance and Detoxification Treatment of Opiate Addiction Under 21 U.S.C. 823(g)(2) (OMB No. 0930– 0234 and OMB No. 0930–0369)— Revision The Drug Addiction Treatment Act of 2000 (‘‘DATA,’’ Pub. L. 106–310) amended the Controlled Substances Act (21 U.S.C. 823(g)(2)) to permit qualifying practitioners to seek and obtain waivers to prescribe certain approved narcotic treatment drugs for the treatment of opiate addiction. The legislation set eligibility requirements and certification requirements as well as an interagency notification review process for practitioners who seek waivers. To implement these provisions, SAMHSA developed Notification of Intent Forms that facilitate the submission and review of notifications. The forms provide the information necessary to determine whether practitioners meets the qualifications for waivers set forth under the law at the E:\FR\FM\03DEN1.SGM 03DEN1 66212 Federal Register / Vol. 84, No. 232 / Tuesday, December 3, 2019 / Notices 30-, 100-, and 275-patient limits. This includes the annual reporting requirements for practitioners with waivers for a 275 patient limit. On October 24, 2018, the Substance Use Disorder Prevention that Promotes Opioid Recovery and Treatment for Patients and Communities (SUPPORT) Act (Pub. L. 115–71) was signed into law. Sections 3201–3202 of the SUPPORT Act made several amendments to the Controlled Substances Act regarding office-based opioid treatment that affords practitioners greater flexibility in the provision of medication-assisted treatment (MAT). The SUPPORT Act expands the definition of ‘‘qualifying other practitioner’’ enabling Clinical Nurse Specialists, Certified Registered Nurse Anesthetists, and Certified Nurse Midwives (CNSs, CRNAs, and CNMs) to apply for a Drug Addiction Treatment Act of 2000 (DATA) waiver until October 1, 2023. It also allows qualified practitioners (i.e., MDs, DOs, NPs, PAs, CNSs, CRNAs, and CNMs) who are board certified in addiction medicine or addiction psychiatry, -or- practitioners who provide MAT in a qualified practice setting, to start treating up to 100 patients in the first year of MAT practice (as defined in 42 CFR 8.2) with a waiver. Further, the SUPPORT Act extends the ability to treat up to 275 patients to 42 CFR citation ‘‘qualifying other practitioners’’ (i.e., NPs, PAs, CNSs, CRNAs, and CNMs) if they have a waiver to treat up 100 patients for at least one year and provide medication-assisted treatment with covered medications (as such terms are defined under 42 CFR 8.2) in a qualified practice setting as described under 42 CFR 8.615. Finally, the SUPPORT Act also expands how physicians could qualify for a waiver. Under the statute now, physicians can qualify for a waiver if they have received at least 8 hours of training on treating and managing opiate-dependent patients, as listed in the statute if the physician graduated in good standing from an accredited school of allopathic medicine or osteopathic medicine in the United States during the 5-year period immediately preceding the date on which the physician submits to SAMHSA. In order to expedite the new provisions of the SUPPORT Act, SAMHSA sought and received a Public Health Emergency Paperwork Reduction Act Waiver. Practitioners may use the form for four types of notifications: (a) New Notification to treat up to 30 patients; (b) New Notification, with the intent to immediately facilitate treatment of an individual (one) patient; (c) Second notification of need and intent to treat up to 100 patients; and (d) New notification to treat up to 100 patients. Under ‘‘new’’ notifications, practitioners may make their initial Estimated number of respondents Purpose of submission waiver requests to SAMHSA. ‘‘Immediate’’ notifications inform SAMHSA and the Attorney General of a practitioner’s intent to prescribe immediately to facilitate the treatment of an individual (one) patient under 21 U.S.C. 823(g)(2)(E)(ii). The form collects data on the following items: Practitioner name; state medical license number; medical specialty; and DEA registration number; address of primary practice location, telephone and fax numbers; email address; name and address of group practice; group practice employer identification number; names and DEA registration numbers of group practitioners; purpose of notification: New, immediate, or renewal; certification of qualifying criteria for treatment and management of opiate dependent patients; certification of capacity to provide directly or refer patients for appropriate counseling and other appropriate ancillary services; certification of maximum patient load, certification to use only those drug products that meet the criteria in the law. The form also notifies practitioners of Privacy Act considerations, and permits practitioners to expressly consent to disclose limited information to the SAMHSA Buprenorphine Physician and Behavioral Health Treatment Services locators. The following table summarizes the estimated annual burden for the use of this form. Burden/ response (hrs.) Responses/ respondent Total burden (hrs.) Notification of Intent .......................................................... Notification to Prescribe Immediately ............................... Notice to Treat up to 100 patients ................................... Notice to Treat up to 275 patients ................................... 1,500 50 500 800 1 1 1 1 0.083 0.083 0.04 1 125 4 20 65 Subtotal ..................................................................... 2,850 ........................ ........................ 214 Burden Associated with the Final Rule That Increased the Patient Limit 8.620 (a)–(c) ..... 8.64 ................... lotter on DSKBCFDHB2PROD with NOTICES 8.655 ................. Request for Patient Limit Increase * ................................. Request for Patient Limit Increase * ................................. Request for Patient Limit Increase * ................................. Renewal Request for a Patient Limit Increase * .............. Renewal Request for a Patient Limit Increase * .............. Renewal Request for a Patient Limit Increase* ............... Request for a Temporary Patient Increase for an Emergency *. Request for a Temporary Patient Increase for an Emergency *. Request for a Temporary Patient Increase for an Emergency *. 517 517 517 260 260 260 10 1 1 1 1 1 1 1 0.5 0.5 0.5 0.5 0.5 0.5 3 259 259 259 130 130 130 30 10 1 3 30 10 1 3 30 Subtotal ..................................................................... 2,361 ........................ ........................ 1,256 New Burden Associated with the Final Rule That Outlined the Reporting Requirements 8.635 ................. VerDate Sep<11>2014 Practitioner Reporting Form * ........................................... ‘‘Qualifying Other Practitioner’’ under 21 U.S.C. 823(g)(2)—Nurse Practitioners. 18:27 Dec 02, 2019 Jkt 250001 PO 00000 Frm 00067 Fmt 4703 Sfmt 4703 1,350 816 E:\FR\FM\03DEN1.SGM 1 1 03DEN1 3 0.066 4,050 54 66213 Federal Register / Vol. 84, No. 232 / Tuesday, December 3, 2019 / Notices 42 CFR citation Estimated number of respondents Purpose of submission ‘‘Qualifying Other Practitioner’’ under 21 U.S.C. 823(g)(2)—Physician Assistants. ‘‘Qualifying Other Practitioner’’ under 21 U.S.C. 823(g)(2)—Certified Nurse Specialists. ‘‘Qualifying Other Practitioner’’ under 21 U.S.C. 823(g)(2)—Certified Nurse Mid-Wives. ‘‘Qualifying Other Practitioner’’ under 21 U.SC. 823(g)(2)—Certified Registered Nurse Anesthetists. Burden/ response (hrs.) Responses/ respondent Total burden (hrs.) 590 1 0.066 39 590 1 0.066 39 590 1 0.066 39 590 1 0.066 39 Subtotal ..................................................................... 4,526 ........................ ........................ 4,260 Total Burden ....................................................... 6,561 ........................ ........................ 5,519 Written comments and recommendations concerning the proposed information collection should be sent by January 2, 2020 to the SAMHSA Desk Officer at the Office of Information and Regulatory Affairs, Office of Management and Budget (OMB). To ensure timely receipt of comments, and to avoid potential delays in OMB’s receipt and processing of mail sent through the U.S. Postal Service, commenters are encouraged to submit their comments to OMB via email to: OIRA_Submission@omb.eop.gov. Although commenters are encouraged to send their comments via email, commenters may also fax their comments to: 202–395–7285. Commenters may also mail them to: Office of Management and Budget, Office of Information and Regulatory Affairs, New Executive Office Building, Room 10102, Washington, DC 20503. Summer King, Statistician. chapter 35). To request a copy of these documents, call the SAMHSA Reports Clearance Officer on (240) 276–1243. Project: Confidentiality of Alcohol and Drug Abuse Patient Records—(OMB No. 0930–0092)—Revision [FR Doc. 2019–26001 Filed 12–2–19; 8:45 am] BILLING CODE 4162–20–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Substance Abuse and Mental Health Services Administration Agency Information Collection Activities: Submission for OMB Review; Comment Request Periodically, the Substance Abuse and Mental Health Services Administration (SAMHSA) will publish a summary of information collection requests under OMB review, in compliance with the Paperwork Reduction Act (44 U.S.C. Statute (42 U.S.C. 290dd–2) and regulations (42 CFR part 2) require federally conducted, regulated, or directly or indirectly assisted alcohol and drug abuse programs to keep alcohol and drug abuse patient records confidential. Information requirements are (1) written disclosure to patients about Federal laws and regulations that protect the confidentiality of each patient, and (2) documenting ‘‘medical personnel’’ status of recipients of a disclosure to meet a medical emergency. Annual burden estimates for these requirements are summarized in the table below: ANNUALIZED BURDEN ESTIMATES Annual number of respondents 1 Responses per respondent Total responses Hours per Response Total hour burden Disclosure 42 CFR 2.22 ........................................................................ 11,779 163 2 1,920,844 .20 384,169 Recordkeeping 42 CFR 2.51 ........................................................................ 11,779 2 23,558 .167 3,934 Total .............................................................................. 11,779 ........................ 1,944,402 ........................ 388,103 1 The lotter on DSKBCFDHB2PROD with NOTICES number of publicly funded alcohol and drug facilities from SAMHSA’s 2017 National Survey of Substance Abuse Treatment Services (N– SSATS). 2 The average number of annual treatment admissions from SAMHSA’s 2015–2017 Treatment Episode Data Set (TEDS). Written comments and recommendations concerning the proposed information collection should be sent by January 2, 2020 to the SAMHSA Desk Officer at the Office of Information and Regulatory Affairs, Office of Management and Budget (OMB). To ensure timely receipt of VerDate Sep<11>2014 18:27 Dec 02, 2019 Jkt 250001 comments, and to avoid potential delays in OMB’s receipt and processing of mail sent through the U.S. Postal Service, commenters are encouraged to submit their comments to OMB via email to: OIRA_Submission@omb.eop.gov. Although commenters are encouraged to send their comments via email, PO 00000 Frm 00068 Fmt 4703 Sfmt 4703 commenters may also fax their comments to: 202–395–7285. Commenters may also mail them to: Office of Management and Budget, Office of Information and Regulatory E:\FR\FM\03DEN1.SGM 03DEN1

Agencies

[Federal Register Volume 84, Number 232 (Tuesday, December 3, 2019)]
[Notices]
[Pages 66211-66213]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2019-26001]


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

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Substance Abuse and Mental Health Services Administration


Agency Information Collection Activities: Submission for OMB 
Review; Comment Request

    Periodically, the Substance Abuse and Mental Health Services 
Administration (SAMHSA) will publish a summary of information 
collection requests under OMB review, in compliance with the Paperwork 
Reduction Act (44 U.S.C. chapter 35). To request a copy of these 
documents, call the SAMHSA Reports Clearance Officer on (240) 276-1243.

Project: Notification of Intent To Use Schedule III, IV, or V Opioid 
Drugs for the Maintenance and Detoxification Treatment of Opiate 
Addiction Under 21 U.S.C. 823(g)(2) (OMB No. 0930-0234 and OMB No. 
0930-0369)--Revision

    The Drug Addiction Treatment Act of 2000 (``DATA,'' Pub. L. 106-
310) amended the Controlled Substances Act (21 U.S.C. 823(g)(2)) to 
permit qualifying practitioners to seek and obtain waivers to prescribe 
certain approved narcotic treatment drugs for the treatment of opiate 
addiction. The legislation set eligibility requirements and 
certification requirements as well as an interagency notification 
review process for practitioners who seek waivers. To implement these 
provisions, SAMHSA developed Notification of Intent Forms that 
facilitate the submission and review of notifications. The forms 
provide the information necessary to determine whether practitioners 
meets the qualifications for waivers set forth under the law at the

[[Page 66212]]

30-, 100-, and 275-patient limits. This includes the annual reporting 
requirements for practitioners with waivers for a 275 patient limit. On 
October 24, 2018, the Substance Use Disorder Prevention that Promotes 
Opioid Recovery and Treatment for Patients and Communities (SUPPORT) 
Act (Pub. L. 115-71) was signed into law. Sections 3201-3202 of the 
SUPPORT Act made several amendments to the Controlled Substances Act 
regarding office-based opioid treatment that affords practitioners 
greater flexibility in the provision of medication-assisted treatment 
(MAT).
    The SUPPORT Act expands the definition of ``qualifying other 
practitioner'' enabling Clinical Nurse Specialists, Certified 
Registered Nurse Anesthetists, and Certified Nurse Midwives (CNSs, 
CRNAs, and CNMs) to apply for a Drug Addiction Treatment Act of 2000 
(DATA) waiver until October 1, 2023. It also allows qualified 
practitioners (i.e., MDs, DOs, NPs, PAs, CNSs, CRNAs, and CNMs) who are 
board certified in addiction medicine or addiction psychiatry, -or- 
practitioners who provide MAT in a qualified practice setting, to start 
treating up to 100 patients in the first year of MAT practice (as 
defined in 42 CFR 8.2) with a waiver.
    Further, the SUPPORT Act extends the ability to treat up to 275 
patients to ``qualifying other practitioners'' (i.e., NPs, PAs, CNSs, 
CRNAs, and CNMs) if they have a waiver to treat up 100 patients for at 
least one year and provide medication-assisted treatment with covered 
medications (as such terms are defined under 42 CFR 8.2) in a qualified 
practice setting as described under 42 CFR 8.615. Finally, the SUPPORT 
Act also expands how physicians could qualify for a waiver. Under the 
statute now, physicians can qualify for a waiver if they have received 
at least 8 hours of training on treating and managing opiate-dependent 
patients, as listed in the statute if the physician graduated in good 
standing from an accredited school of allopathic medicine or 
osteopathic medicine in the United States during the 5-year period 
immediately preceding the date on which the physician submits to 
SAMHSA. In order to expedite the new provisions of the SUPPORT Act, 
SAMHSA sought and received a Public Health Emergency Paperwork 
Reduction Act Waiver. Practitioners may use the form for four types of 
notifications: (a) New Notification to treat up to 30 patients; (b) New 
Notification, with the intent to immediately facilitate treatment of an 
individual (one) patient; (c) Second notification of need and intent to 
treat up to 100 patients; and (d) New notification to treat up to 100 
patients. Under ``new'' notifications, practitioners may make their 
initial waiver requests to SAMHSA. ``Immediate'' notifications inform 
SAMHSA and the Attorney General of a practitioner's intent to prescribe 
immediately to facilitate the treatment of an individual (one) patient 
under 21 U.S.C. 823(g)(2)(E)(ii). The form collects data on the 
following items: Practitioner name; state medical license number; 
medical specialty; and DEA registration number; address of primary 
practice location, telephone and fax numbers; email address; name and 
address of group practice; group practice employer identification 
number; names and DEA registration numbers of group practitioners; 
purpose of notification: New, immediate, or renewal; certification of 
qualifying criteria for treatment and management of opiate dependent 
patients; certification of capacity to provide directly or refer 
patients for appropriate counseling and other appropriate ancillary 
services; certification of maximum patient load, certification to use 
only those drug products that meet the criteria in the law. The form 
also notifies practitioners of Privacy Act considerations, and permits 
practitioners to expressly consent to disclose limited information to 
the SAMHSA Buprenorphine Physician and Behavioral Health Treatment 
Services locators. The following table summarizes the estimated annual 
burden for the use of this form.

----------------------------------------------------------------------------------------------------------------
                                                     Estimated                        Burden/
      42 CFR citation            Purpose of          number of      Responses/       response      Total burden
                                 submission         respondents     respondent        (hrs.)          (hrs.)
----------------------------------------------------------------------------------------------------------------
                            Notification of                1,500               1           0.083             125
                             Intent.
                            Notification to                   50               1           0.083               4
                             Prescribe
                             Immediately.
                            Notice to Treat up               500               1            0.04              20
                             to 100 patients.
                            Notice to Treat up               800               1               1              65
                             to 275 patients.
                                                 ---------------------------------------------------------------
                               Subtotal.........           2,850  ..............  ..............             214
----------------------------------------------------------------------------------------------------------------
                     Burden Associated with the Final Rule That Increased the Patient Limit
----------------------------------------------------------------------------------------------------------------
8.620 (a)-(c).............  Request for Patient              517               1             0.5             259
                             Limit Increase *.
                            Request for Patient              517               1             0.5             259
                             Limit Increase *.
                            Request for Patient              517               1             0.5             259
                             Limit Increase *.
8.64......................  Renewal Request for              260               1             0.5             130
                             a Patient Limit
                             Increase *.
                            Renewal Request for              260               1             0.5             130
                             a Patient Limit
                             Increase *.
                            Renewal Request for              260               1             0.5             130
                             a Patient Limit
                             Increase*.
8.655.....................  Request for a                     10               1               3              30
                             Temporary Patient
                             Increase for an
                             Emergency *.
                            Request for a                     10               1               3              30
                             Temporary Patient
                             Increase for an
                             Emergency *.
                            Request for a                     10               1               3              30
                             Temporary Patient
                             Increase for an
                             Emergency *.
                                                 ---------------------------------------------------------------
                               Subtotal.........           2,361  ..............  ..............           1,256
----------------------------------------------------------------------------------------------------------------
               New Burden Associated with the Final Rule That Outlined the Reporting Requirements
----------------------------------------------------------------------------------------------------------------
8.635.....................  Practitioner                   1,350               1               3           4,050
                             Reporting Form *.
                            ``Qualifying Other               816               1           0.066              54
                             Practitioner''
                             under 21 U.S.C.
                             823(g)(2)--Nurse
                             Practitioners.

[[Page 66213]]

 
                            ``Qualifying Other               590               1           0.066              39
                             Practitioner''
                             under 21 U.S.C.
                             823(g)(2)--Physicia
                             n Assistants.
                            ``Qualifying Other               590               1           0.066              39
                             Practitioner''
                             under 21 U.S.C.
                             823(g)(2)--Certifie
                             d Nurse Specialists.
                            ``Qualifying Other               590               1           0.066              39
                             Practitioner''
                             under 21 U.S.C.
                             823(g)(2)--Certifie
                             d Nurse Mid-Wives.
                            ``Qualifying Other               590               1           0.066              39
                             Practitioner''
                             under 21 U.SC.
                             823(g)(2)--Certifie
                             d Registered Nurse
                             Anesthetists.
                                                 ---------------------------------------------------------------
                               Subtotal.........           4,526  ..............  ..............           4,260
                                                 ---------------------------------------------------------------
                                 Total Burden...           6,561  ..............  ..............           5,519
----------------------------------------------------------------------------------------------------------------

    Written comments and recommendations concerning the proposed 
information collection should be sent by January 2, 2020 to the SAMHSA 
Desk Officer at the Office of Information and Regulatory Affairs, 
Office of Management and Budget (OMB). To ensure timely receipt of 
comments, and to avoid potential delays in OMB's receipt and processing 
of mail sent through the U.S. Postal Service, commenters are encouraged 
to submit their comments to OMB via email to: 
[email protected]. Although commenters are encouraged to send 
their comments via email, commenters may also fax their comments to: 
202-395-7285. Commenters may also mail them to: Office of Management 
and Budget, Office of Information and Regulatory Affairs, New Executive 
Office Building, Room 10102, Washington, DC 20503.

Summer King,
Statistician.
[FR Doc. 2019-26001 Filed 12-2-19; 8:45 am]
 BILLING CODE 4162-20-P