Meeting of the Secretary's Advisory Committee on Human Research Protections, 38031-38032 [2014-15593]
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Federal Register / Vol. 79, No. 128 / Thursday, July 3, 2014 / Notices
Mr.
Curtis E. Glover Sr. Procurement
Analyst, Contract Policy Division, GSA
202–501–1448 or email
Curtis.glover@gsa.gov.
SUPPLEMENTARY INFORMATION:
FOR FURTHER INFORMATION CONTACT:
A. Purpose
Federal agencies use the Standard
Form (SF) 330 to obtain information
from architect-engineer (A–E) firms
about their professional qualifications.
Federal agencies select firms for A–E
contracts on the basis of professional
qualifications as required by 40 U.S.C.
Chapter 11, Selection of Architects
Engineers, and Part 36 of the Federal
Acquisition Regulation (FAR).
SF 330, Part I is used by all Executive
agencies to obtain information from
architect-engineer firms interested in a
particular project. The information on
the form is reviewed by a selection
panel to assists in the selection of the
most qualified architect-engineer firm to
perform the specific project. The form is
designed to provide a uniform method
for architect-engineer firms to submit
information on experience, personnel,
and capabilities of the architectengineer firm to perform, along with
information on the consultants they
expect to collaborate with on the
specific project.
SF 330, Part II is used by all Executive
agencies to obtain general uniform
information about a firm’s experience in
architect-engineering projects.
Architect-engineer firms are encouraged
to update the form annually. The
information obtained on this form is
used to determine if a firm should be
solicited for architect-engineer projects.
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B. Annual Reporting Burden
Respondents: 5,000.
Responses per Respondent: 4.
Total Responses: 20,000.
Hours per Response: 29.
Total Burden Hours: 580,000.
C. Public Comments
Public comments are particularly
invited on: Whether this collection of
information is necessary for the proper
performance of functions of the FAR,
and whether it will have practical
utility; whether our estimate of the
public burden of this collection of
information is accurate, and based on
valid assumptions and methodology;
ways to enhance the quality, utility, and
clarity of the information to be
collected; and ways in which we can
minimize the burden of the collection of
information on those who are to
respond, through the use of appropriate
technological collection techniques or
other forms of information technology.
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Obtaining Copies Of Proposals:
Requesters may obtain a copy of the
information collection documents from
the General Services Administration,
Regulatory Secretariat Division (MVCB),
1800 F Street NW., Washington, DC
20405. Please cite OMB Control No.
9000–0157, Architect-Engineer
Qualifications (SF 330), in all
correspondence.
Dated: June 27, 2014.
Karlos Morgan,
Acting Director, Federal Acquisition Policy
Division, Office of Government-wide
Acquisition Policy, Office of Acquisition
Policy, Office of Government-wide Policy.
38031
heading of the bulletin portion, remove
‘‘Add date signed’’ and add ‘‘April 10,
2014.’’ in its place.
3. On page 21469, in the second
column, first line, remove ‘‘Associate
Administrator.’’ and add ‘‘Associate
Administrator, Office of Governmentwide Policy.’’ in its place.
Dated: June 26, 2014.
Carolyn Austin-Diggs,
Acting Deputy Associate Administrator,
Office of Asset and Transportation
Management, Office of Government-wide
Policy.
[FR Doc. 2014–15645 Filed 7–2–14; 8:45 am]
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[FR Doc. 2014–15641 Filed 7–2–14; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
GENERAL SERVICES
ADMINISTRATION
[Notice–PBS–2013–02; Docket No: 2013–
0002; Sequence 12]
Federal Management Regulation;
Delegations of Lease Acquisition
Authority—Notification, Usage, and
Reporting Requirements for General
Purpose, Categorical, and Special
Purpose Space Delegations;
Corrections
Public Buildings Service (PBS),
General Services Administration (GSA).
ACTION: Notice of FMR Bulletin C–2;
Corrections.
AGENCY:
GSA published a notice in the
Federal Register on April 16, 2014,
regarding Delegations of Lease
Acquisition Authority—Notification,
Usage, and Reporting Requirements for
General Purpose, Categorical, and
Special Purpose Space Delegations. GSA
is making corrections to the
Supplementary Information section of
the document.
DATE: Effective: July 3, 2014.
FOR FURTHER INFORMATION CONTACT:
Contact Ms. Mary Pesina, Director,
Center for Lease Delegations, Office of
Leasing, Public Buildings Service, at
202–236–1686, or mary.pesina@gsa.gov.
SUPPLEMENTARY INFORMATION:
SUMMARY:
Corrections
In the notice FR Doc. 2014–08645
published in the Federal Register at 79
FR 21464, April 16, 2014, make the
following corrections:
1. On page 21465, in the first column,
remove ‘‘Anne E. Rung, Associate
Administrator.’’ and add ‘‘Anne E.
Rung, Associate Administrator, Office of
Government-wide Policy.’’ in its place.
2. On page 21465, in the first column,
under General Services Administration
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Meeting of the Secretary’s Advisory
Committee on Human Research
Protections
Office of the Secretary, Office
of the Assistant Secretary for Health,
Department of Health and Human
Services.
ACTION: Notice.
AGENCY:
Pursuant to Section 10(a) of
the Federal Advisory Committee Act,
U.S.C. Appendix 2, notice is hereby
given that the Secretary’s Advisory
Committee on Human Research
Protections (SACHRP) will hold a
meeting that will be open to the public.
Information about SACHRP and the full
meeting agenda will be posted on the
SACHRP Web site at: https://
www.dhhs.gov/ohrp/sachrp/mtgings/
index.html.
DATES: The meeting will be held on
Monday, July 21, 2014, from 8:30 a.m.
until 5:00 p.m. and Tuesday, July 22,
2014, from 8:30 a.m. until 4:00 p.m.
ADDRESSES: Note new location! Fisher’s
Lane Conference Center, Terrace Level,
5635 Fisher Lane, Rockville, MD 20852.
FOR FURTHER INFORMATION CONTACT: Jerry
Menikoff, M.D., J.D., Executive
Secretary, SACHRP and Director, Office
for Human Research Protections
(OHRP), or Julia Gorey, J.D., Executive
Director, SACHRP; U.S. Department of
Health and Human Services, 1101
Wootton Parkway, Suite 200, Rockville,
Maryland 20852; 240–453–8141; fax:
240–453–6909; email address:
Julia.Gorey@hhs.gov.
SUPPLEMENTARY INFORMATION: Under the
authority of 42 U.S.C. 217a, Section 222
of the Public Health Service Act, as
amended, SACHRP was established to
provide expert advice and
recommendations to the Secretary of
Health and Human Services, through
SUMMARY:
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38032
Federal Register / Vol. 79, No. 128 / Thursday, July 3, 2014 / Notices
the Assistant Secretary for Health, on
issues and topics pertaining to or
associated with the protection of human
research subjects.
The meeting will open to the public
at 8:30 a.m., on Monday, July 21.
Following opening remarks from Dr.
Jerry Menikoff, Executive Secretary,
SACHRP and OHRP Director, and Dr.
Jeffrey Botkin, SACHRP Chair, the
Subpart A Subcommittee (SAS) will
give their initial report on the new SAS
initiative examining informed consent.
A panel of speakers will discuss
comprehension and tools for validating
comprehension in informed consent.
SAS is charged with developing
recommendations for consideration by
SACHRP regarding the application of
subpart A of 45 CFR part 46 in the
current research environment; this
subcommittee was established by
SACHRP in October 2006.
On the afternoon of July 21, the
Subcommittee on Harmonization (SOH)
will present their initial work on the
topic of the intersection of the HHS and
FDA regulations and ‘‘big data’’; this
presentation will be highlighted by a
special expert panel discussion. The
morning of July 22, the SOH will
present their work to date on the topic
of return of general results, also assisted
by a special expert panel discussion.
SOH was established by SACHRP at its
July 2009 meeting and is charged with
identifying and prioritizing areas in
which regulations and/or guidelines for
human subjects research adopted by
various agencies or offices within HHS
would benefit from harmonization,
consistency, clarity, simplification, and/
or coordination.
A public comment session will be
offered on both days.
Public attendance at the meeting is
limited to space available. Individuals
who plan to attend and need special
assistance, such as sign language
interpretation or other reasonable
accommodations, should notify the
SACHRP at the address/phone listed
above at least one week prior to the
meeting. Pre-registration is required for
participation in the on-site public
comment session; individuals may preregister the day of the meeting or by
contacting the Executive Director,
SACHRP, by COB July 17. Individuals
who would like to submit written
statements should email or fax their
comments to SACHRP at least five
business days prior to the meeting.
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Dated: June 27, 2014.
Julia Gorey,
Executive Director, Secretary’s Advisory
Committee on Human Research Protections.
[FR Doc. 2014–15593 Filed 7–2–14; 8:45 am]
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
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[CDC–2014–0010, Docket Number NIOSH
063–C]
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institute for Occupational
Safety and Health Meeting
Meeting of the Advisory Committee on
Minority Health; Correction
Department of Health and
Human Services, Office of the Secretary,
Office of the Assistant Secretary for
Health, Office of Minority Health.
AGENCY:
ACTION:
Notice; correction.
The Department of Health and
Human Services published a notice in
the Federal Register, dated June 17,
2014, to announce a meeting of the
Advisory Committee on Minority Health
that will be held on Tuesday, July 8,
2014, from 9 a.m. to 5 p.m., and on
Wednesday, July 9, 2014, from 9 a.m. to
4 p.m. The meeting is scheduled to be
held at the Omni Shoreham Hotel, 2500
Calvert Street NW., Washington, DC
20008. The posted meeting times have
been changed.
Dr.
Rashida Dorsey, OMH–ACMH@hhs.gov,
Tower Building; 1101 Wootton
Parkway, Suite 600; Rockville, MD
20852; Phone: 240–453–8222; Fax: 240–
453–8223.https://www.pacha.gov.
FOR FURTHER INFORMATION CONTACT:
Correction
In the Federal Register, dated June 17,
2014, FR Doc. 2014–14066, on page
34531, in the second column, correct
the posted meeting times noted under
the DATES caption to read:
Tuesday, July 8, 2014, from 9
a.m. to 3 p.m., and on Wednesday, July
9, 2014, from 9 a.m. to 3 p.m.
DATES:
Dated: June 26, 2014.
Rashida Dorsey,
Designated Federal Officer, Advisory
Committee on Minority Health.
[FR Doc. 2014–15592 Filed 7–2–14; 8:45 am]
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The National Institute for
Occupational Safety and Health
(NIOSH) of the Centers for Disease
Control and Prevention (CDC)
announces the following web-based
public meeting and request for public
comment on the NIOSH Fire Fighter
Fatality Investigation and Prevention
Program (FFFIPP) and also announces
the availability of a report entitled
‘‘NIOSH Fire Fighter Fatality
Investigation and Prevention Program
(FFFIPP) Progress Report and Proposed
Future Directions—2014’’ which is now
available for public comment. To view
the notice and related materials, visit
https://www.regulations.gov and enter
CDC–2014–0010 in the search field and
click ‘‘Search.’’
DATES: Meeting date and time: August
20, 2014, 1:00 p.m.-4:00 p.m. EDT.
Public comment period: Comments
must be received by 11:59 p.m. on
October 20, 2014.
ADDRESSES: You may submit comments,
identified by CDC–2014–0010 and
Docket Number NIOSH 063–C, by either
of the following two methods:
• Federal eRulemaking Portal:
https://www.regulations.gov. Follow the
instructions for submitting comments.
• Mail: National Institute for
Occupational Safety and Health, NIOSH
Docket Office, 1090 Tusculum Avenue,
MS C–34, Cincinnati, Ohio 45226–1998.
Instructions: All information received
in response to this notice must include
the agency name and docket number
(CDC–2014–0010; NIOSH 063–C). All
relevant comments received will be
posted without change to https://
www.regulations.gov, including any
personal information provided. All
electronic comments should be
formatted as Microsoft Word. Please
make reference to CDC–2014–0010 and
Docket Number NIOSH 063–C. All
information received in response to this
notice will also be available for public
SUMMARY:
SUMMARY:
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The National Institute for
Occupational Safety and Health
(NIOSH) of the Centers for Disease
Control and Prevention (CDC),
Department of Health and Human
Services (HHS).
ACTION: Notice of public meeting and
draft document for comment.
AGENCY:
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Agencies
[Federal Register Volume 79, Number 128 (Thursday, July 3, 2014)]
[Notices]
[Pages 38031-38032]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2014-15593]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Meeting of the Secretary's Advisory Committee on Human Research
Protections
AGENCY: Office of the Secretary, Office of the Assistant Secretary for
Health, Department of Health and Human Services.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: Pursuant to Section 10(a) of the Federal Advisory Committee
Act, U.S.C. Appendix 2, notice is hereby given that the Secretary's
Advisory Committee on Human Research Protections (SACHRP) will hold a
meeting that will be open to the public. Information about SACHRP and
the full meeting agenda will be posted on the SACHRP Web site at:
https://www.dhhs.gov/ohrp/sachrp/mtgings/.
DATES: The meeting will be held on Monday, July 21, 2014, from 8:30
a.m. until 5:00 p.m. and Tuesday, July 22, 2014, from 8:30 a.m. until
4:00 p.m.
ADDRESSES: Note new location! Fisher's Lane Conference Center, Terrace
Level, 5635 Fisher Lane, Rockville, MD 20852.
FOR FURTHER INFORMATION CONTACT: Jerry Menikoff, M.D., J.D., Executive
Secretary, SACHRP and Director, Office for Human Research Protections
(OHRP), or Julia Gorey, J.D., Executive Director, SACHRP; U.S.
Department of Health and Human Services, 1101 Wootton Parkway, Suite
200, Rockville, Maryland 20852; 240-453-8141; fax: 240-453-6909; email
address: Julia.Gorey@hhs.gov.
SUPPLEMENTARY INFORMATION: Under the authority of 42 U.S.C. 217a,
Section 222 of the Public Health Service Act, as amended, SACHRP was
established to provide expert advice and recommendations to the
Secretary of Health and Human Services, through
[[Page 38032]]
the Assistant Secretary for Health, on issues and topics pertaining to
or associated with the protection of human research subjects.
The meeting will open to the public at 8:30 a.m., on Monday, July
21. Following opening remarks from Dr. Jerry Menikoff, Executive
Secretary, SACHRP and OHRP Director, and Dr. Jeffrey Botkin, SACHRP
Chair, the Subpart A Subcommittee (SAS) will give their initial report
on the new SAS initiative examining informed consent. A panel of
speakers will discuss comprehension and tools for validating
comprehension in informed consent. SAS is charged with developing
recommendations for consideration by SACHRP regarding the application
of subpart A of 45 CFR part 46 in the current research environment;
this subcommittee was established by SACHRP in October 2006.
On the afternoon of July 21, the Subcommittee on Harmonization
(SOH) will present their initial work on the topic of the intersection
of the HHS and FDA regulations and ``big data''; this presentation will
be highlighted by a special expert panel discussion. The morning of
July 22, the SOH will present their work to date on the topic of return
of general results, also assisted by a special expert panel discussion.
SOH was established by SACHRP at its July 2009 meeting and is charged
with identifying and prioritizing areas in which regulations and/or
guidelines for human subjects research adopted by various agencies or
offices within HHS would benefit from harmonization, consistency,
clarity, simplification, and/or coordination.
A public comment session will be offered on both days.
Public attendance at the meeting is limited to space available.
Individuals who plan to attend and need special assistance, such as
sign language interpretation or other reasonable accommodations, should
notify the SACHRP at the address/phone listed above at least one week
prior to the meeting. Pre-registration is required for participation in
the on-site public comment session; individuals may pre-register the
day of the meeting or by contacting the Executive Director, SACHRP, by
COB July 17. Individuals who would like to submit written statements
should email or fax their comments to SACHRP at least five business
days prior to the meeting.
Dated: June 27, 2014.
Julia Gorey,
Executive Director, Secretary's Advisory Committee on Human Research
Protections.
[FR Doc. 2014-15593 Filed 7-2-14; 8:45 am]
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