Agency Information Collection Activities: Proposed Collection; Comment Request, 7169-7170 [2012-3141]
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Federal Register / Vol. 77, No. 28 / Friday, February 10, 2012 / Notices
organization and the rare disease(s) or
condition(s) that they represent. The
information provided should address
the eligibility and selection criteria
below.
Organizations must meet the
following eligibility criteria to submit a
response.
srobinson on DSK4SPTVN1PROD with NOTICES
Eligibility Criteria
a. Represent a rare disease/condition
as defined by law (affects fewer than
200,000 individuals in the United
States).
b. Maintain a hard copy or an
electronic email list of patients affected
by the specific disease/condition.
c. Be willing to seek agreement by
their members to share their deidentified data with the GRDR, other
databases, and the research community
as part of an Institutional Review Board
(IRB) approved informed consent.
d. Agree to adopt the ORDR Common
Data Elements and elements of the
ORDR common consent form template.
e. Have a scientific or medical
advisory board to assist on ethical issues
of privacy human subject protection,
data coding and transmission, as well as
issues related to data standards,
curation, coding and transmission,
scientific issues related to research
proposals, and other issues as needed.
Organizations that meet the eligibility
criteria are asked to provide a short
description of how they will address the
selection criteria which are listed below.
Please note that the response for each
criterion has a word limit and each
criterion will be weighed accordingly as
indicated.
1. Have a well-defined, credible
vision and purpose for establishing a
registry. (300 words, weigh 30 points)
2. Have a good plan to sustain the
newly established or already existing
registry beyond the 2 years of the pilot
project. (150 words, weigh 20 points)
3. Have, or plan to develop, a feasible
system to capture patient updates of
their medical information as well as
updates of patients’ medical information
from healthcare providers. (150 words,
weigh 10 points)
4. Agree to assist in the translation of
their registry into multiple languages as
needed to facilitate the inclusion of nonEnglish speaking participants and
appear to be capable of providing such
assistance. The GRDR will use English
only. (150 words, weigh 10 points)
5. Have a good plan for data
verification by an individual with a
medical background. (150 words, weigh
10 points)
6. Are engaged or willing to
collaborate with other organizations
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21:29 Feb 09, 2012
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serving the same or related diseases.
(150 words, weigh 10 points)
7. Have a developed means of
communication with the public, e.g.
electronic mailing lists, newsletter, Web
site and other social networking media.
(150 words, weigh 5 points)
8. Have, or plan for, support to
navigate both future registry activities
and community outreach. (150 words,
weigh 5 points)
The selection committee, comprised
of individuals with medical
background, patient advocacy leaders,
and others, will rank the submissions
from the patient groups based on the
selection criteria. ORDR will make the
final selections of the patient groups
based on rare disease categories to
achieve maximum distribution of the
different rare diseases. In addition, an
effort will be made to ensure that large
and small patient organizations will be
included, i.e., half from organizations
that represent a rare disease with more
than 2,500 patient participants and half
from organizations with less than 2,500
patient participants (based on hard copy
or the electronic contact list).
This invitation and related
background information will be
available on the ORDR Web site
https://rarediseases.info.nih.gov/GRDR
and distributed through various
communication tools. Selected
organizations will be notified and their
names will be posted on the ORDR Web
site.
How To Submit a Response: Reponses
will be accepted for 30 days following
publication of this notice. All responses
must be submitted via the Web site at:
https://rarediseases.info.nih.gov/GRDR.
An online form will be available to
submit the requested information.
Submitters are requested not to exceed
the number of characters indicated on
the online form. Submitted information
will not be considered confidential
although each submission will be stored
using a login and a password.
This Request for Information (RFI)
notice provides information and
selection criteria only. It should not be
construed as a solicitation or as an
obligation on the part of the Federal
Government, the NIH, or the ORDR. The
ORDR does not intend to make any
awards to pay for the preparation of any
information submitted or for the
Government’s use of such information.
ORDR will use the information
submitted in response to this RFI at its
discretion and will not provide
comments to any responder’s
submission. However, names of patient
organizations that are selected in
response to this RFI will be posted on
the Web site at: https://
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7169
rarediseases.info.nih.gov/GRDR. The
ORDR may contact any responder for
the sole purpose of enhancing the
ORDR’s understanding of the RFI
submission. Respondents will receive
an automated email confirmation
acknowledging receipt of their response,
but will not receive individualized
feedback. No proprietary, classified,
confidential, or sensitive information
should be included in your response.
DATES: Responses to this notice must be
received on or before 30 days following
publication of this notice.
FOR FURTHER INFORMATION CONTACT:
Yaffa Rubinstein, Ph.D., Director of
Patient Resources for Clinical and
Translational Research, Office of Rare
Diseases Research, National Institutes of
Health, 6100 Executive Boulevard,
Room 3A07, Rockville, MD 20892–7518,
telephone 301–402–4338, Fax 301–480–
9655, Web site https://
rarediseases.info.nih.gov.
Dated: February 1, 2012.
Thomas Insel,
Acting Director, National Center for
Advancing Translational Sciences (NCATS),
National Institutes of Health.
[FR Doc. 2012–3155 Filed 2–9–12; 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
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
E:\FR\FM\10FEN1.SGM
10FEN1
7170
Federal Register / Vol. 77, No. 28 / Friday, February 10, 2012 / Notices
collection of information on
respondents, including through the use
of automated collection techniques or
other forms of information technology.
Proposed 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)—Extension
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
practitioners (physicians) to seek and
obtain waivers to prescribe certain
approved narcotic treatment drugs for
the treatment of opiate addiction. The
legislation sets eligibility requirements
and certification requirements as well as
an interagency notification review
process for physicians who seek
waivers. The legislation was amended
in 2005 to eliminate the patient limit for
physicians in group practices, and in
2006, to permit certain physicians to
treat up to 100 patients.
To implement these provisions,
SAMHSA developed a notification form
(SMA–167) that facilitates the
submission and review of notifications.
The form provides the information
necessary to determine whether
practitioners (i.e., independent
physicians) meet the qualifications for
waivers set forth under the new law.
Use of this form will enable physicians
to know they have provided all
information needed to determine
whether practitioners are eligible for a
waiver.
However, there is no prohibition on
use of other means to provide requisite
information. The Secretary will convey
notification information and
determinations to the Drug Enforcement
Administration (DEA), which will
assign an identification number to
qualifying practitioners; this number
will be included in the practitioner’s
registration under 21 U.S.C. 823(f).
Practitioners may use the form for
three types of notification: (a) New, (b)
immediate, and (c) to notify of their
intent 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). Finally,
the form may be used by physicians
with waivers to certify their need and
intent to treat up to 100 patients.
The form collects data on the
following items: Practitioner name; state
medical license number and DEA
registration number; address of primary
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
Number of
respondents
Purpose of submission
practitioners; purpose of notification
new, immediate, or renewal;
certification of qualifying criteria for
treatment and management of opiate
dependent patients; certification of
capacity to 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
Locator.
Since July 2002, SAMHSA has
received over 25,000 notifications and
has certified almost 27,000 physicians.
Fifty-none percent of the notifications
were submitted by mail or by facsimile,
with approximately forty-one percent
submitted through the Web based online
system. Approximately 60 percent of the
certified physicians have consented to
disclosure on the SAMHSA
Buprenorphine Physician Locator.
Respondents may submit the form
electronically, through a dedicated Web
page that SAMHSA will establish for the
purpose, as well as via U.S. mail.
There are no changes to the forms and
burden hours.
The following table summarizes the
estimated annual burden for the use of
this form.
Responses
per
respondent
Burden per
response (hr.)
Total burden
(hrs)
Initial Application for Waiver ............................................................................
Notification to Prescribe Immediately ..............................................................
Notice to Treat up to 100 patients ...................................................................
1,500
50
500
1
1
1
.083
.083
.040
125
4
20
Total ..........................................................................................................
2,050
—
—
149
Send comments to Summer King,
SAMHSA Reports Clearance Officer,
Room 8–1099, One Choke Cherry Road,
Rockville, MD 20857 or email a copy to
summer.king@samhsa.hhs.gov. Written
comments must be received before 60
days after the date of the publication in
the Federal Register.
srobinson on DSK4SPTVN1PROD with NOTICES
Janine Denis Cook,
Chemist.
DEPARTMENT OF HOMELAND
SECURITY
Coast Guard
National Boating Safety Advisory
Council; Vacancies
Coast Guard, DHS.
Request for applications.
AGENCY:
[FR Doc. 2012–3141 Filed 2–9–12; 8:45 am]
BILLING CODE 4162–20–P
SUMMARY:
VerDate Mar<15>2010
21:29 Feb 09, 2012
The Coast Guard seeks
applications for membership on the
National Boating Safety Advisory
Council (NBSAC). This Council advises
the Coast Guard on recreational boating
safety regulations and other major
boating safety matters.
Jkt 226001
PO 00000
Frm 00056
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Sfmt 4703
Applicants should send
their cover letter and resume to the
following address: Commandant (CG–
5422)/NBSAC, Attn: Mr. Jeff Ludwig,
U.S. Coast Guard, 2100 Second St. SW.,
Stop 7581, Washington, DC 20593–
7581. You can also call 202–372–1061;
or email jeffrey.a.ludwig@uscg.mil. This
notice is available in our online docket,
USCG–2010–0316, at https://
www.regulations.gov. Members of the
public should not submit personal
information into a docket, as it becomes
public record.
ADDRESSES:
[Docket No. USCG–2010–0316]
ACTION:
Applicants should submit a
cover letter and resume in time to reach
the Alternate Designated Federal Officer
(ADFO) on or before April 10, 2012.
DATES:
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10FEN1
Agencies
[Federal Register Volume 77, Number 28 (Friday, February 10, 2012)]
[Notices]
[Pages 7169-7170]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-3141]
-----------------------------------------------------------------------
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
[[Page 7170]]
collection of information on respondents, including through the use of
automated collection techniques or other forms of information
technology.
Proposed 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)--Extension
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 practitioners (physicians) to seek and obtain waivers to
prescribe certain approved narcotic treatment drugs for the treatment
of opiate addiction. The legislation sets eligibility requirements and
certification requirements as well as an interagency notification
review process for physicians who seek waivers. The legislation was
amended in 2005 to eliminate the patient limit for physicians in group
practices, and in 2006, to permit certain physicians to treat up to 100
patients.
To implement these provisions, SAMHSA developed a notification form
(SMA-167) that facilitates the submission and review of notifications.
The form provides the information necessary to determine whether
practitioners (i.e., independent physicians) meet the qualifications
for waivers set forth under the new law. Use of this form will enable
physicians to know they have provided all information needed to
determine whether practitioners are eligible for a waiver.
However, there is no prohibition on use of other means to provide
requisite information. The Secretary will convey notification
information and determinations to the Drug Enforcement Administration
(DEA), which will assign an identification number to qualifying
practitioners; this number will be included in the practitioner's
registration under 21 U.S.C. 823(f).
Practitioners may use the form for three types of notification: (a)
New, (b) immediate, and (c) to notify of their intent 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). Finally, the form may be used by
physicians with waivers to certify their need and intent to treat up to
100 patients.
The form collects data on the following items: Practitioner name;
state medical license number and DEA registration number; address of
primary 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 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 Locator.
Since July 2002, SAMHSA has received over 25,000 notifications and
has certified almost 27,000 physicians. Fifty-none percent of the
notifications were submitted by mail or by facsimile, with
approximately forty-one percent submitted through the Web based online
system. Approximately 60 percent of the certified physicians have
consented to disclosure on the SAMHSA Buprenorphine Physician Locator.
Respondents may submit the form electronically, through a dedicated
Web page that SAMHSA will establish for the purpose, as well as via
U.S. mail.
There are no changes to the forms and burden hours.
The following table summarizes the estimated annual burden for the
use of this form.
----------------------------------------------------------------------------------------------------------------
Number of Responses per Burden per Total burden
Purpose of submission respondents respondent response (hr.) (hrs)
----------------------------------------------------------------------------------------------------------------
Initial Application for Waiver.................. 1,500 1 .083 125
Notification to Prescribe Immediately........... 50 1 .083 4
Notice to Treat up to 100 patients.............. 500 1 .040 20
---------------------------------------------------------------
Total....................................... 2,050 -- -- 149
----------------------------------------------------------------------------------------------------------------
Send comments to Summer King, SAMHSA Reports Clearance Officer,
Room 8-1099, One Choke Cherry Road, Rockville, MD 20857 or email a copy
to summer.king@samhsa.hhs.gov. Written comments must be received before
60 days after the date of the publication in the Federal Register.
Janine Denis Cook,
Chemist.
[FR Doc. 2012-3141 Filed 2-9-12; 8:45 am]
BILLING CODE 4162-20-P