Informational Meeting: The Importation and Exportation of Infectious Biological Agents, Infectious Substances and Vectors; Public Webcast, 35360-35361 [2016-13053]
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Federal Register / Vol. 81, No. 106 / Thursday, June 2, 2016 / Notices
confidential information. All the other
completed model trust certificates and
model trust documents (except for any
trust provisions that relate to the
testamentary disposition of trust assets)
are retained and made publicly
available based upon a proper request
under EIGA (by filling out an OGE Form
201 access form) until the periods for
retention of all other reports (usually the
OGE Form 278 Public Financial
Disclosure Reports) of the individual
establishing the trust have lapsed
(generally six years after the filing of the
last other report). See 5 CFR
2634.603(g)(2) of OGE’s executive
branch financial disclosure regulation.
The U.S. Office of Government Ethics
administers the qualified trust program
for the executive branch. At the present
time, there are no active filers using the
trust model certificates and documents.
However, OGE intends to submit to
OMB a request for extension of approval
for two reasons. First, under OMB’s
implementing regulations for the
Paperwork Reduction Act, at 5 CFR
1320.3(c)(4)(i), any recordkeeping,
reporting or disclosure requirement
contained in a sponsoring agency rule of
general applicability is deemed to meet
the minimum threshold of ten or more
persons. Second, OGE does anticipate
possible limited use of these forms
during the forthcoming three-year
period 2016–2019. Therefore, the
estimated burden figures, representing
branchwide implementation of the
forms, will remain the same as
previously reported by OGE in its prior
first and second round paperwork
renewal notice for the trust forms (77 FR
76293–76294 (December 27, 2012) and
78 FR 40144–40146 (July 3, 2013)). The
estimate is based on the amount of time
imposed on a trust administrator or
private representative.
i. Trust Certificates:
A. Certificate of Independence: Total
filers (executive branch): 5; private
citizen filers (100%): 5; private citizen
burden hours (20 minutes/certificate): 2.
B. Certificate of Compliance: Total
filers (executive branch): 10; private
citizen filers (100%): 10; private citizen
burden hours (20 minutes/certificate): 3;
and
ii. Model Qualified Trust Documents:
A. Blind Trust Communications: Total
users (executive branch): 5; private
citizen users (100%): 5;
communications documents (private
citizens): 25 (based on an average of five
communications per user, per year);
private citizen burden hours (20
minutes/communication): 8.
B. Model Qualified Blind Trust: Total
users (executive branch): 2; private
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citizen users (100%): 2; private citizen
burden hours (100 hours/model): 200.
C. Model Qualified Diversified Trust:
Total users (executive branch): 1;
private citizen users (100%): 1; private
citizen burden hours (100 hours/model):
100.
D.–H. Of the five remaining model
qualified trust documents: Total users
(executive branch): 2; private citizen
users (100%): 2; private citizen burden
hours (100 hours/model): 200.
I.–J. Of the two model confidentiality
agreements: Total users (executive
branch): 1; private citizen users (100%):
1; private citizen burden hours (50
hours/agreement): 50.
However, the total annual reporting
hour burden on filers themselves is zero
and not the 563 hours estimated above
because OGE’s estimating methodology
reflects the fact that all respondents hire
private trust administrators or other
private representatives to set up and
maintain the qualified blind and
diversified trusts. Respondents
themselves, typically incoming private
citizen Presidential nominees, therefore
incur no hour burden. The estimated
total annual cost burden to respondents
resulting from the collection of
information is $1,000,000. Those who
use the model documents for guidance
are private trust administrators or other
private representatives hired to set up
and maintain the qualified blind and
diversified trusts of executive branch
officials who seek to establish such
qualified trusts. The cost burden figure
is based primarily on OGE’s knowledge
of the typical trust administrator fee
structure (an average of 1 percent of
total assets) and OGE’s experience with
administration of the qualified trust
program. The $1,000,000 annual cost
figure is based on OGE’s estimate of an
average of five possible active trusts
anticipated to be under administration
for each of the next three years with
combined total assets of $100,000,000.
However, OGE notes that the $1,000,000
figure is a cost estimate for the overall
administration of the trusts, only a
portion of which relates to information
collection and reporting. For want of a
precise way to break out the costs
directly associated with information
collection, OGE is continuing to report
to OMB the full $1,000,000 estimate for
paperwork clearance purposes.
On March 4, 2016, OGE published a
first round notice of its intent to request
paperwork clearance for the proposed
unmodified qualified trust certificates
and modified model trust documents.
See 81 FR 11566–11567. OGE did not
receive any responses to that notice.
In this second notice, public comment
is again invited on the model qualified
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trust certificates and model trust
documents, and underlying regulatory
provisions, as set forth in this notice,
including specific views on the need for
and practical utility of this set of
collections of information, the accuracy
of OGE’s burden estimate, the potential
for enhancement of quality, utility and
clarity of the information collected, and
the minimization of burden (including
the use of information technology).
Comments received in response to
this notice will be summarized for, and
may be included with, the OGE request
for extension of the OMB paperwork
approval for the set of the various
existing qualified trust model
certificates, the model communications
package, and the model trust
documents. The comments will also
become a matter of public record.
Approved: May 27, 2016.
Walter M. Shaub, Jr.
Director, Office of Government Ethics.
[FR Doc. 2016–13008 Filed 6–1–16; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
Informational Meeting: The Importation
and Exportation of Infectious
Biological Agents, Infectious
Substances and Vectors; Public
Webcast
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
ACTION: Notice of public webcast.
AGENCY:
The Centers for Disease
Control and Prevention (CDC),
Department of Health and Human
Services (HHS) is hosting a public
webcast to address import and export
permit regulations for infectious
biological agents, infectious substances,
and vectors; and import and export
permit exemptions. Presenters for this
webcast will include representatives
from the U.S. Department of
Transportation (DOT), United States
Department of Agriculture (USDA)
Animal and Plant Health Inspection
Service (APHIS), CDC Division of Global
Migration and Quarantine, U.S. Customs
and Border Protection, U.S. Department
of Commerce, U.S. Food and Drug
Administration, HHS/Office of the
Assistant Secretary for Preparedness
and Response/Biomedical Advanced
Research and Development Authority
(BARDA), U.S. Fish and Wildlife
SUMMARY:
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Service, and the Public Health Agency
of Canada.
DATES: The webcast will be held over
two days, August 3, 2016 from 12 p.m.
to 4 p.m. EDT and August 4, 2016 from
12:00 p.m. to 4:00 p.m. Registration
instructions are found on the HHS/CDC
Import Permit Program Web site, https://
www.cdc.gov/od/eaipp/
importApplication/agents.htm.
ADDRESSES: The webcast will be
broadcast from the Centers for Disease
Control and Prevention, 1600 Clifton
Road NE., Atlanta, Georgia 30329.
FOR FURTHER INFORMATION CONTACT: Von
McClee, Division of Select Agents and
Toxins, Office of Public Health
Preparedness and Response, Centers for
Disease Control and Prevention, 1600
Clifton Road, NE., MS A–46, Atlanta,
GA 30333; phone: 404–718–2000; email:
lrsat@cdc.gov.
SUPPLEMENTARY INFORMATION: This
webcast is an opportunity for all
interested parties (e.g., academic
institutions and biomedical centers,
commercial manufacturing facilities,
federal, state, and local laboratories,
including clinical and diagnostic
laboratories, research facilities,
exhibition facilities, and educational
facilities) to obtain specific guidance
and information regarding import and
export permit regulations. The webcast
will also provide assistance to those
interested in applying for an import or
export permit (or license) from federal
agencies within the United States.
Instructions for registration are found
on the HHS/CDC Import Permit Program
Web site, https://www.cdc.gov/od/eaipp/
importApplication/agents.htm.
Participants must register by July 15,
2016. This is a webcast only event and
there will be no on-site participation at
the HHS/CDC broadcast facility.
Dated: May 27, 2016.
Veronica Kennedy,
Acting Executive Secretary, Centers for
Disease Control and Prevention.
[FR Doc. 2016–13053 Filed 6–1–16; 8:45 am]
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public comment in response to the
notice. This notice collects comments
on the information collection
requirements relating to the
continuation of an existing collection
for University Centers for Excellence in
Developmental Disabilities Education,
Research, and Service.
DATES: Submit written comments on the
collection of information by August 1,
2016.
Submit written comments
on the collection of information by
email to Valerie.Bond@acl.hhs.gov.
FOR FURTHER INFORMATION CONTACT:
Valerie Bond by email at Valerie.Bond@
acl.hhs.gov or 202.795–7311.
SUPPLEMENTARY INFORMATION: Section
104 (42 U.S.C. 15004) of the
Developmental Disabilities Assistance
and Bill of Rights Act of 2000 (DD Act
of 2000) directs the Secretary of Health
and Human Services to develop and
implement a system of program
accountability to monitor the grantees
funded under the DD Act of 2000. The
program accountability system shall
include the National Network of
University Centers for Excellence in
Developmental Disabilities Education,
Research, and Service (UCEDDs)
authorized under Part D of the DD Act
of 2000. In addition to the
accountability system, Section 154(e)
(42 U.S.C. 15064) of the DD Act of 2000
includes requirements for a UCEDD
Annual Report.
ACL estimates the burden of this
collection of information as follows:
ADDRESSES:
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Community Living
Agency Information Collection
Activities: Submission for OMB
Review; Comment Request; University
Centers for Excellence in
Developmental Disabilities Education,
Research, and Service—Annual Report
Administration for Community
Living, HHS.
ACTION: Notice.
AGENCY:
The Administration on
Intellectual and Developmental
Disabilities (AIDD), Administration for
Community Living (ACL) is announcing
an opportunity to comment on the
proposed collection of information by
the agency. Under the Paperwork
Reduction Act of 1995 (the PRA),
Federal agencies are required to publish
notice in the Federal Register
concerning each proposed collection of
information, including each proposed
extension of an existing collection of
information, and to allow 60 days for
SUMMARY:
Annual Burden Estimates
ANNUAL BURDEN ESTIMATES
Instrument
Number of
respondents
Number of
responses per
respondent
Average
burden hours
per response
Total burden
hours
UCEDD Annual Report ....................................................................................
67
1
1,412
94,604
Estimated Total Annual Burden
Hours: 94,604.
Dated: May 25, 2016.
Kathy Greenlee,
Administrator & Assistant Secretary for
Aging.
asabaliauskas on DSK3SPTVN1PROD with NOTICES
[FR Doc. 2016–13020 Filed 6–1–16; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Community Living
Agency Information Collection
Activities; Submission for OMB
Review; Comment Request; Senior
Medicare Patrol (SMP) Program
Outcome Measurement
Administration for Community
Living, HHS.
ACTION: Notice.
AGENCY:
The Administration for
Community Living (ACL) is announcing
that the proposed collection of
SUMMARY:
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information listed below has been
submitted to the Office of Management
and Budget (OMB) for review and
clearance under the Paperwork
Reduction Act of 1995.
DATES: Submit written comments on the
collection of information by July 5,
2016.
Submit written comments
on the collection of information by fax
202.395.5806 or by email to OIRA_
submission@omb.eop.gov. Attn: OMB
Desk Officer for ACL.
FOR FURTHER INFORMATION CONTACT:
Phillip McKoy at 202.795.7397 or email:
phillip.mckoy@acl.hhs.gov.
ADDRESSES:
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Agencies
[Federal Register Volume 81, Number 106 (Thursday, June 2, 2016)]
[Notices]
[Pages 35360-35361]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-13053]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
Informational Meeting: The Importation and Exportation of
Infectious Biological Agents, Infectious Substances and Vectors; Public
Webcast
AGENCY: Centers for Disease Control and Prevention (CDC), Department of
Health and Human Services (HHS).
ACTION: Notice of public webcast.
-----------------------------------------------------------------------
SUMMARY: The Centers for Disease Control and Prevention (CDC),
Department of Health and Human Services (HHS) is hosting a public
webcast to address import and export permit regulations for infectious
biological agents, infectious substances, and vectors; and import and
export permit exemptions. Presenters for this webcast will include
representatives from the U.S. Department of Transportation (DOT),
United States Department of Agriculture (USDA) Animal and Plant Health
Inspection Service (APHIS), CDC Division of Global Migration and
Quarantine, U.S. Customs and Border Protection, U.S. Department of
Commerce, U.S. Food and Drug Administration, HHS/Office of the
Assistant Secretary for Preparedness and Response/Biomedical Advanced
Research and Development Authority (BARDA), U.S. Fish and Wildlife
[[Page 35361]]
Service, and the Public Health Agency of Canada.
DATES: The webcast will be held over two days, August 3, 2016 from 12
p.m. to 4 p.m. EDT and August 4, 2016 from 12:00 p.m. to 4:00 p.m.
Registration instructions are found on the HHS/CDC Import Permit
Program Web site, https://www.cdc.gov/od/eaipp/importApplication/agents.htm.
ADDRESSES: The webcast will be broadcast from the Centers for Disease
Control and Prevention, 1600 Clifton Road NE., Atlanta, Georgia 30329.
FOR FURTHER INFORMATION CONTACT: Von McClee, Division of Select Agents
and Toxins, Office of Public Health Preparedness and Response, Centers
for Disease Control and Prevention, 1600 Clifton Road, NE., MS A-46,
Atlanta, GA 30333; phone: 404-718-2000; email: lrsat@cdc.gov.
SUPPLEMENTARY INFORMATION: This webcast is an opportunity for all
interested parties (e.g., academic institutions and biomedical centers,
commercial manufacturing facilities, federal, state, and local
laboratories, including clinical and diagnostic laboratories, research
facilities, exhibition facilities, and educational facilities) to
obtain specific guidance and information regarding import and export
permit regulations. The webcast will also provide assistance to those
interested in applying for an import or export permit (or license) from
federal agencies within the United States.
Instructions for registration are found on the HHS/CDC Import
Permit Program Web site, https://www.cdc.gov/od/eaipp/importApplication/agents.htm. Participants must register by July 15, 2016. This is a
webcast only event and there will be no on-site participation at the
HHS/CDC broadcast facility.
Dated: May 27, 2016.
Veronica Kennedy,
Acting Executive Secretary, Centers for Disease Control and Prevention.
[FR Doc. 2016-13053 Filed 6-1-16; 8:45 am]
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