Agency Information Collection Activities: Proposed Collection; Comment Request, 31842-31843 [07-2871]

Download as PDF 31842 Federal Register / Vol. 72, No. 110 / Friday, June 8, 2007 / Notices drug products for use in the treatment of arthritis, rheumatism, and related diseases. 7. Cardiovascular and Renal Drugs Advisory Committee Reviews and evaluates available data concerning the safety and effectiveness of marketed and investigational human drug products for use in the treatment of cardiovascular and renal disorders. 8. Dermatologic and Ophthalmic Drugs Advisory Committee Reviews and evaluates available data concerning the safety and effectiveness of marketed and investigational human drug products for use in the treatment of dermatologic and ophthalmic disorders. 9. Drug Safety and Risk Management Advisory Committee Advises the Commissioner of Food and Drugs (the Commissioner) regarding the scientific and medical evaluation of all information gathered by the Department of Health and Human Services and the Department of Justice with the regard to safety, efficacy, and abuse potential, risk management, risk communication, and quantitative evaluation of spontaneous reports, and recommends actions to be taken by FDA with regard to marketing, investigation, and control of such drugs or other substances. 10. Endocrinologic and Metabolic Drugs Advisory Committee Reviews and evaluates available data concerning the safety and effectiveness of marketed and investigational human drug products for use in the treatment of endocrine and metabolic disorders. 11. Gastrointestinal Drugs Advisory Committee Reviews and evaluates available data concerning the safety and effectiveness of marketed and investigational human drug products for use in the treatment of gastrointestinal disorders. pwalker on PROD1PC71 with NOTICES 12. Nonprescription Drugs Advisory Committee Reviews and evaluates available data concerning the safety and effectiveness of over-the-counter (nonprescription) human drug products for use in the treatment of a broad spectrum of human symptoms and diseases. 13. Oncologic Drugs Advisory Committee Reviews and evaluates available data concerning the safety and effectiveness of marketed and investigational human drug products for use in the treatment of cancer. VerDate Aug<31>2005 18:14 Jun 07, 2007 Jkt 211001 14. Peripheral and Central Nervous System Drugs Advisory Committee Reviews and evaluates available data concerning the safety and effectiveness of marketed and investigational human drug products for use in the treatment of neurologic diseases. 15. Psychopharmacologic Drugs Advisory Committee Reviews and evaluates available data concerning the safety and effectiveness of marketed and investigational human drug products for use in the practice of psychiatry and related fields. 16. Pulmonary-Allergy Drugs Advisory Committee Reviews and evaluates available data concerning the safety and effectiveness of marketed and investigational human drug products for use in the treatment of pulmonary disease and diseases with allergic and/or immunologic mechanisms. II. Selection Procedure Any industry organization interested in participating in the selection of an appropriate nonvoting member to represent industry interests should send a letter stating that interest to the FDA contact (see FOR FURTHER INFORMATION CONTACT) within 30 days of publication of this document (see DATES). Within the subsequent 30 days, FDA will send a letter to each organization that has expressed and interest, attaching a complete list of all such organizations; and a list of all nominees along with their current resumes. The letter will also state that it is the responsibility of the interested organizations to confer with one another and to select a candidate, within 60 days after the receipt of the FDA letter, to serve as the nonvoting member to represent industry interests for a particular committee. The interested organizations are not bound by the list of nominees in selecting a candidate. However, if no individual is selected within 60 days, the Commissioner will select the nonvoting member to represent industry interests. III. Application Procedure Individuals may self nominate and/or an organization may nominate one or more individuals to serve as a nonvoting industry representative. A current curriculum vitae and the name of the committee of interest should be sent to the FDA contact person (see FOR FURTHER INFORMATION CONTACT) within 30 days (see DATES). FDA will forward all nominations to the organizations expressing interest in participating in the selection process for that committee. (Persons who nominate themselves as PO 00000 Frm 00048 Fmt 4703 Sfmt 4703 nonvoting industry representatives will not participate in the selection process.) FDA has a special interest in ensuring that women, minority groups, individuals with physical disabilities, and small businesses are adequately represented on its advisory committees, and therefore, encourages nominations for appropriately qualified candidates from these groups. Specifically, in this document, nominations for nonvoting representatives of industry interests are encouraged from the drug manufacturing industry. This notice is issued under the Federal Advisory Committee Act (5 U.S.C. app. 2) and 21 CFR part 14, relating to advisory committees. Dated: May 28, 2007. Randall W. Lutter, Associate Commissioner for Policy and Planning. [FR Doc. E7–11065 Filed 6–7–07; 8:45 am] BILLING CODE 4160–01–S 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: Participant Feedback on Training Under the Cooperative Agreement for Mental E:\FR\FM\08JNN1.SGM 08JNN1 31843 Federal Register / Vol. 72, No. 110 / Friday, June 8, 2007 / Notices Health Care Provider Education in HIV/ AIDS Program (OMB No. 0930–0195)— Extension The Substance Abuse and Mental Health Services Administration’s (SAMHSA) Center for Mental Health Services (CMHS) intends to continue to conduct a multi-site assessment for the Mental Health Care Provider Education in HIV/AIDS Program. These education programs are designed to disseminate knowledge of the psychological and neuropsychiatric sequelae of HIV/AIDS to both traditional (e.g., psychiatrists, psychologists, nurses, primary care physicians, medical students, and social workers) and non-traditional (e.g., clergy, and alternative health care workers) first-line providers of mental health services, in particular to providers in minority communities. The multi-site assessment is designed to assess the effectiveness of particular training curricula, document the integrity of training delivery formats, and assess the effectiveness of the various training delivery formats. Analyses will assist CMHS in documenting the numbers and types of traditional and non-traditional mental health providers accessing training; the content, nature and types of training participants receive; and the extent to which trainees experience knowledge, skill and attitude gains/changes as a result of training attendance. The multisite data collection design uses a twotiered data collection and analytic strategy to collect information on (1) the organization and delivery of training, and (2) the impact of training on participant’s knowledge, skills and abilities. Information about the organization and delivery of training will be collected from trainers and staff, hence there is no respondent burden. All training participants will be asked to complete a brief feedback form at the end of the training session. CMHS anticipates funding 10 education sites for the Mental Health Care Provider Education in HIV/AIDS Program. The annual burden estimates for this activity are shown below: Responses per respondent Estimated number of respondents × 10 sites) Session Report Form ............................................................................................. Participant Feedback Form (General Education) .................................................. Neuropsychiatric Participant Feedback Form ....................................................... Non Physician Neuropsychiatric Participant Feedback Form ............................... Adherence Participant Feedback Form ................................................................. Ethics Participant Feedback Form ........................................................................ 1 1 1 1 1 1 60 × 10 = 600 500 × 10 = 5000 160 × 10 = 1600 240 × 10 = 2400 100 × 10 = 1000 200 × 10 = 2000 0.080 0.167 0.167 0.167 0.167 0.167 48 835 267 401 167 125 Total ................................................................................................................ .................... 12,600 .................... 1,843 Form Send comments to Summer King, SAMHSA Reports Clearance Officer, Room 7–1044, One Choke Cherry Road, Rockville, MD 20857 and e-mail her a copy at summer.king@samhsa.hhs.gov. Written comments should be received within 60 days of this notice. Dated: May 30, 2007. Elaine Parry, Acting Director, Office of Program Services. [FR Doc. 07–2871 Filed 6–7–07; 8:45 am] BILLING CODE 4162–20–M DEPARTMENT OF HEALTH AND HUMAN SERVICES Substance Abuse and Mental Health Services Administration pwalker on PROD1PC71 with NOTICES 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 VerDate Aug<31>2005 18:14 Jun 07, 2007 Jkt 211001 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: 2007 National Survey of Mental Health Treatment Facilities (NSMHTF) (OMB No. 0930–0119)— Revision The Substance Abuse and Mental Health Services Administration’s (SAMHSA) Center for Mental Health Services (CMHS) will conduct a 2007 NSMHTF. This national survey represents a re-design of the biennial Survey of Mental Health Organizations (SMHO) last conducted in 2004 under OMB No. 0930–0119. Instead of surveying each mental health organization as a whole, the 2007 NSMHTF will survey all of the mental health treatment locations. These PO 00000 Frm 00049 Fmt 4703 Sfmt 4703 Hours per response Total hours separate mental health service locations are called facilities, in contrast to mental health organizations, which may include multiple facilities (service locations). This survey will be (a) a 100 percent enumeration of all known mental health treatment facilities nationwide, (b) more consumer-oriented in describing services available at each facility location, and (c) patterned after SAMHSA’s Office of Applied Studies National Survey of Substance Abuse Treatment Services (OMB No. 0930– 0106). The 2007 NSMHTF will utilize one questionnaire for all mental health treatment facility types including hospitals, residential treatment centers and outpatient clinics. The information collected will include intake telephone numbers for services, types of services offered and acceptable forms of payment, emergency hotline numbers, facility caseload, and facility bed counts, if applicable. All treatment facilities will be contacted by telephone prior to the mailing to verify their eligibility, and facility type. The resulting database will be used to provide both state and national estimates of facility types and their patient caseloads. Information from the 2007 survey will also be used to update the National Mental Health Information Center’s facility locator for consumers. In addition, data derived from the E:\FR\FM\08JNN1.SGM 08JNN1

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[Federal Register Volume 72, Number 110 (Friday, June 8, 2007)]
[Notices]
[Pages 31842-31843]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 07-2871]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Substance Abuse and Mental Health Services Administration


Agency Information Collection Activities: Proposed Collection; 
Comment Request

    In compliance with section 3506(c)(2)(A) of the Paperwork Reduction 
Act of 1995 concerning 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: Participant Feedback on Training Under the 
Cooperative Agreement for Mental

[[Page 31843]]

Health Care Provider Education in HIV/AIDS Program (OMB No. 0930-
0195)--Extension
    The Substance Abuse and Mental Health Services Administration's 
(SAMHSA) Center for Mental Health Services (CMHS) intends to continue 
to conduct a multi-site assessment for the Mental Health Care Provider 
Education in HIV/AIDS Program. These education programs are designed to 
disseminate knowledge of the psychological and neuropsychiatric 
sequelae of HIV/AIDS to both traditional (e.g., psychiatrists, 
psychologists, nurses, primary care physicians, medical students, and 
social workers) and non-traditional (e.g., clergy, and alternative 
health care workers) first-line providers of mental health services, in 
particular to providers in minority communities.
    The multi-site assessment is designed to assess the effectiveness 
of particular training curricula, document the integrity of training 
delivery formats, and assess the effectiveness of the various training 
delivery formats. Analyses will assist CMHS in documenting the numbers 
and types of traditional and non-traditional mental health providers 
accessing training; the content, nature and types of training 
participants receive; and the extent to which trainees experience 
knowledge, skill and attitude gains/changes as a result of training 
attendance. The multi-site data collection design uses a two-tiered 
data collection and analytic strategy to collect information on (1) the 
organization and delivery of training, and (2) the impact of training 
on participant's knowledge, skills and abilities.
    Information about the organization and delivery of training will be 
collected from trainers and staff, hence there is no respondent burden. 
All training participants will be asked to complete a brief feedback 
form at the end of the training session. CMHS anticipates funding 10 
education sites for the Mental Health Care Provider Education in HIV/
AIDS Program. The annual burden estimates for this activity are shown 
below:

----------------------------------------------------------------------------------------------------------------
                                                         Responses    Estimated number
                         Form                               per      of respondents  x   Hours per   Total hours
                                                         respondent      10 sites)        response
----------------------------------------------------------------------------------------------------------------
Session Report Form...................................            1      60 x 10 = 600        0.080           48
Participant Feedback Form (General Education).........            1    500 x 10 = 5000        0.167          835
Neuropsychiatric Participant Feedback Form............            1    160 x 10 = 1600        0.167          267
Non Physician Neuropsychiatric Participant Feedback               1    240 x 10 = 2400        0.167          401
 Form.................................................
Adherence Participant Feedback Form...................            1    100 x 10 = 1000        0.167          167
Ethics Participant Feedback Form......................            1    200 x 10 = 2000        0.167          125
                                                                    -------------------             ------------
    Total.............................................  ...........             12,600  ...........        1,843
----------------------------------------------------------------------------------------------------------------

    Send comments to Summer King, SAMHSA Reports Clearance Officer, 
Room 7-1044, One Choke Cherry Road, Rockville, MD 20857 and e-mail her 
a copy at summer.king@samhsa.hhs.gov. Written comments should be 
received within 60 days of this notice.

    Dated: May 30, 2007.
Elaine Parry,
Acting Director, Office of Program Services.
[FR Doc. 07-2871 Filed 6-7-07; 8:45 am]
BILLING CODE 4162-20-M