Decision To Evaluate a Petition To Designate a Class of Employees for the Metals and Controls Corporation in Attleboro, MA, To Be Included in the Special Exposure Cohort, 44846-44847 [E9-20899]
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Federal Register / Vol. 74, No. 167 / Monday, August 31, 2009 / Notices
site (https://ntp.niehs.nih.gov/go/29679).
Comments on the draft background
document should be sent to Dr. Ruth M.
Lunn, NIEHS, P.O. Box 12233, MD K2–
14, Research Triangle Park, NC 27709,
FAX: (919) 541–0144, or
lunn@niehs.nih.gov. Courier address:
Report on Carcinogens Center, 530
Davis Drive, Room 2006, Morrisville,
NC 27560. Persons needing interpreting
services in order to attend should
contact (301) 402–8180 (voice) or (301)
435–1908 (TTY). Requests should be
made at least seven business days in
advance of the meeting.
Dr.
Ruth M. Lunn, Director, RoC Center,
(919) 316–4637, lunn@niehs.nih.gov.
FOR FURTHER INFORMATION CONTACT:
SUPPLEMENTARY INFORMATION:
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Background
The NTP announced the RoC review
process for the 12th RoC on April 16,
2007, in the Federal Register (72 FR
18999, available at https://
ntp.niehs.nih.gov/go/15208). As part of
that process, an expert panel meeting is
being convened on November 2–4, 2009,
to review formaldehyde for possible
listing in the 12th RoC. The draft
background document for formaldehyde
will be available on the RoC Web site by
September 3, 2009, or in printed text
from the RoC Center (see ADDRESSES
above). Persons can register free-ofcharge with the NTP listserv (https://
ntp.niehs.nih.gov/go/231) to receive
notification when draft RoC background
documents for candidate substances and
meetings related to the 12th RoC are
made available on the RoC Web site.
Formaldehyde is a high production
chemical with a wide array of uses. The
predominant use of formaldehyde in the
United States is in the production of
industrial resins (mainly urea, phenol,
polyacetal, and melamine resins) that
are used primarily to manufacture
products such as adhesives and binders
for wood products. Other uses include
as a chemical intermediate, in
agriculture (for example as a fumigant),
in the production of paraformaldehyde
and chelating agents, embalming and
fixative or preservative in the medical
and research fields, and as a
preservative in numerous consumer
products such as cleaning agents and
cosmetic products. Formaldehyde has
been detected in indoor and outdoor air,
surface water and groundwater, soil,
and food products and is generally
considered to be ubiquitous in the
environment. Formaldehyde (gas) is
currently listed in the 11th RoC as
reasonably anticipated to be a human
carcinogen and was nominated for
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14:57 Aug 28, 2009
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reclassification of its listing status in the
12th RoC.
Preliminary Agenda and Registration
Preliminary agenda topics include:
• Oral public comments on
formaldehyde;
• Peer review of the draft background
document on formaldehyde;
• Recommendation on the listing
status of formaldehyde in the 12th RoC
and scientific justification.
The meeting is scheduled for
November 2–4, 2009, from 8:30 a.m. to
adjournment each day. It is anticipated
that the meeting will adjourn by 4 p.m.
on November 4, although adjournment
may occur earlier or later depending
upon the time needed for the expert
panel to complete its work. A copy of
the preliminary agenda, expert panel
roster, and any additional information,
when available, will be posted on the
RoC Web site or may be requested from
the Director of the RoC Center (see
ADDRESSES above). Individuals who
plan to attend the meeting are
encouraged to register on-line by
October 26, 2009, to facilitate planning
for the meeting.
Request for Comments
The NTP invites both written and oral
public comments on the draft
background document on formaldehyde.
Persons submitting written comments
are asked to include their name and
contact information (affiliation, mailing
address, telephone and facsimile
numbers, e-mail, and sponsoring
organization, if any) and send them to
Dr. Lunn (see ADDRESSES above) for
receipt by October 16, 2009. All written
comments identified by the individual’s
name and affiliation or sponsoring
organization (if applicable) will be
posted on the RoC Web site prior to the
meeting and distributed to the expert
panel and RoC staff for their
consideration in the peer review of the
draft background document and/or
preparation for the meeting.
Time will be set aside at the expert
panel meeting for the presentation of
oral public comments. Seven minutes
will be available for each speaker (one
speaker per organization). Persons can
register on-line to present oral
comments or by contacting Dr. Lunn
(see ADDRESSES above). When
registering to comment orally, please
provide your name, affiliation, mailing
address, telephone number, e-mail and
sponsoring organization (if any). If
possible, send a copy of the statement
or talking points to Dr. Lunn by October
26, 2009. This statement will be
provided to the expert panel to assist
them in identifying issues for discussion
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and will be noted in the meeting record.
Registration for presentation of oral
comments will also be available at the
meeting on November 2–4, 2009, from
7:30–8:30 a.m. Time allowed for
comments by on-site registrants may be
less than for pre-registered speakers and
will be determined by the number of
persons who register at the meeting to
give oral comments. Persons registering
at the meeting are asked to bring 25
copies of their statement or talking
points for distribution to the expert
panel and for the record.
Background Information on the RoC
The RoC is a congressionally
mandated document [Section 301(b)(4)
of the Public Health Services Act, 42
U.S.C. 241(b)(4)], that identifies and
discusses agents, substances, mixtures,
or exposure circumstances (collectively
referred to as ‘‘substances’’) that may
pose a hazard to human health by virtue
of their carcinogenicity. Substances are
listed in the report as either known or
reasonably anticipated to be human
carcinogens. The NTP prepares the RoC
on behalf of the Secretary of Health and
Human Services. Information about the
RoC and the nomination process can be
obtained from its homepage (https://
ntp.niehs.nih.gov/go/roc) or by
contacting Dr. Lunn (see For Further
Information Contact above). The NTP
follows a formal, multi-step process for
review and evaluation of selected
substances. The formal evaluation
process is available on the RoC Web site
(https://ntp.niehs.nih.gov/go/15208) or in
printed copy from the RoC Center.
Dated: August 21, 2009.
John R. Bucher,
Associate Director, National Toxicology
Program.
[FR Doc. E9–20878 Filed 8–28–09; 8:45 am]
BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institute for Occupational
Safety and Health
Decision To Evaluate a Petition To
Designate a Class of Employees for
the Metals and Controls Corporation in
Attleboro, MA, To Be Included in the
Special Exposure Cohort
AGENCY: National Institute for
Occupational Safety and Health
(NIOSH), Department of Health and
Human Services (HHS).
ACTION: Notice.
SUMMARY: HHS gives notice as required
by 42 CFR 83.12(e) of a decision to
E:\FR\FM\31AUN1.SGM
31AUN1
Federal Register / Vol. 74, No. 167 / Monday, August 31, 2009 / Notices
evaluate a petition to designate a class
of employees for the Metals and
Controls Corporation in Attleboro,
Massachusetts, to be included in the
Special Exposure Cohort under the
Energy Employees Occupational Illness
Compensation Program Act of 2000. The
initial proposed definition for the class
being evaluated, subject to revision as
warranted by the evaluation, is as
follows:
Facility: Metals and Controls
Corporation.
Location: Attleboro, Massachusetts.
Job Titles and/or Job Duties: All
Atomic Weapons Employer employees
who were exposed to thorium.
Period of Employment: January 1,
1952 through December 31, 1967.
FOR FURTHER INFORMATION CONTACT:
Larry Elliott, Director, Office of
Compensation Analysis and Support,
National Institute for Occupational
Safety and Health (NIOSH), 4676
Columbia Parkway, MS C–46,
Cincinnati, OH 45226, Telephone 513–
533–6800 (this is not a toll-free
number). Information requests can also
be submitted by e-mail to
OCAS@CDC.GOV.
Christine M. Branche,
Acting Director, National Institute for
Occupational Safety and Health.
[FR Doc. E9–20899 Filed 8–28–09; 8:45 am]
BILLING CODE 4163–19–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Office of Research Integrity; Privacy
Act of 1974; Report of an Altered
System of Records
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AGENCY: Office of Research Integrity
(ORI), Office of Public Health and
Science (OPHS), Office of the Secretary
(OS), Department of Health and Human
Services (HHS).
ACTION: Notice of revision to the Privacy
Act system of records.
SUMMARY: HHS proposes to revise the
Privacy Act exempt system of records
09–37–0021, entitled ‘‘Public Health
Service Records Related to Inquiries and
Investigations of Scientific Misconduct,
HHS/OASH/ORI.’’ This system became
effective on August 29, 1994 (59 FR
36717, July 19, 1994). Changes were
made in response to comments received,
and the revised systems notice was
published on January 6, 1995 (60 FR
2140). The proposed revisions include
changing the routine uses and changing
the title of the system to ‘‘HHS Records
Related to Research Misconduct
Proceedings, HHS/OS/ORI.’’ The
revisions are necessary to reflect the
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changes made by the Public Health
Service Policies on Research
Misconduct (‘‘PHS Policies on Research
Misconduct’’), 42 CFR Part 93 (‘‘Part
93’’), and to update the system to reflect
current practices and procedures under
that regulation.
DATES: This notice will be effective
without further notice on September 30,
2009 unless modified by a subsequent
notice making changes in response to
public comments. Although the Privacy
Act requires only that changes in the
routine uses be published for comment,
HHS invites comments on all parts of
the systems notice. You may submit
comments by electronic mail to
AskORI@hhs.gov. Comments must be
received on or before September 30,
2009.
FOR FURTHER INFORMATION CONTACT:
Director, Division of Investigative
Oversight, Office of Research Integrity,
1101 Wootton Parkway, Suite 750,
Rockville, MD 20852. (240) 453–8800.
E-mail: AskORI@hhs.gov.
SUPPLEMENTARY INFORMATION: After
making changes in response to public
comments, ORI published its current
systems notice entitled ‘‘Public Health
Service Records Related to Inquiries and
Investigations of Scientific Misconduct,
HHS/OASH/ORI’’ on January 6, 1995
(60 FR 2140). Since that time, the
organizational location of ORI has
changed from the former Office of the
Assistant Secretary for Health to OPHS,
and a new HHS regulation concerning
research misconduct was promulgated
and codified at 42 CFR Part 93. That
regulation substantially changed the
previous regulation on scientific
misconduct (42 CFR Part 50, Subpart A),
including changing the term
‘‘misconduct in science’’ to ‘‘research
misconduct.’’
This revision updates the ORI system
notice to be consistent with the
definitions and procedures promulgated
by the PHS Policies on Research
Misconduct. The description of the
categories of individuals covered by the
records system and categories of records
in the system have been amended to
reflect the changes made by Part 93,
specifically, the applicability of that
part in terms of the individuals, types of
research, and types of PHS support that
are covered. Pertinent provisions of Part
93 are referenced to explain the records
system coverage. The category of
individuals covered by the system
remains the same: individuals who are
the subject of allegations of research
misconduct. Similarly, the categories of
records in the system remain essentially
the same: records related to all stages of
the research misconduct proceeding.
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44847
The location of the system is now
limited to the premises of ORI and the
Federal Records Centers (for inactive
records). PHS officials outside of ORI
who are involved in extramural and
intramural research misconduct
proceedings have access to this system
of records as necessary to carry out their
duties.
We have amended the statement of
purposes to state more generally that
ORI will use the system of records to
exercise its oversight authority relating
to research misconduct proceedings,
and to document these activities.
The order of the routine uses has been
changed, and the terminology used has
been updated to reflect the terms used
in Part 93. The listing of routine uses
begins with disclosures that may be
made in the course of a research
misconduct proceeding in roughly the
order that they might occur, and ends
with disclosures that may be necessary
for more general administrative
purposes.
Routine use 1 is an expanded version
of routine uses 2 and 5 in the current
system notice. It now provides for
disclosure to a person able to ‘‘obtain’’
information, as well as provide
information or assistance, in a research
misconduct proceeding or related
proceeding, ORI oversight of an
institutional research misconduct
proceeding or ORI oversight of the
implementation of HHS administrative
actions. The reference to ORI oversight
functions has also been added. We have
also added a condition for each
disclosure under this routine use. Prior
to disclosure, ORI will determine
whether limited disclosures or
confidentiality agreements are needed to
protect the privacy of respondent(s),
complainant(s), witnesses, research
subjects or others who may be identified
in the records to be disclosed.
Routine use 2 is new. It is based on
42 CFR 93.401 that, in part, authorizes
ORI to notify and consult with other
Federal, State, or local offices, if ORI has
reason to believe that a research
misconduct proceeding may involve
that office. The second routine use in
the current system notice, relating to
disclosures to qualified experts, has
been deleted because that disclosure is
now covered by the more general
disclosure in the new routine uses 1 and
9.
Except for editorial changes, routine
use 3 is the same as use 8 in the current
system notice and routine use 4 is the
same as use 3 in the current notice.
Routine use 5 is new. It permits
additional disclosures after a final HHS/
ORI finding of research misconduct that
are aimed at conserving public funds,
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Agencies
[Federal Register Volume 74, Number 167 (Monday, August 31, 2009)]
[Notices]
[Pages 44846-44847]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E9-20899]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institute for Occupational Safety and Health
Decision To Evaluate a Petition To Designate a Class of Employees
for the Metals and Controls Corporation in Attleboro, MA, To Be
Included in the Special Exposure Cohort
AGENCY: National Institute for Occupational Safety and Health (NIOSH),
Department of Health and Human Services (HHS).
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: HHS gives notice as required by 42 CFR 83.12(e) of a decision
to
[[Page 44847]]
evaluate a petition to designate a class of employees for the Metals
and Controls Corporation in Attleboro, Massachusetts, to be included in
the Special Exposure Cohort under the Energy Employees Occupational
Illness Compensation Program Act of 2000. The initial proposed
definition for the class being evaluated, subject to revision as
warranted by the evaluation, is as follows:
Facility: Metals and Controls Corporation.
Location: Attleboro, Massachusetts.
Job Titles and/or Job Duties: All Atomic Weapons Employer employees
who were exposed to thorium.
Period of Employment: January 1, 1952 through December 31, 1967.
FOR FURTHER INFORMATION CONTACT: Larry Elliott, Director, Office of
Compensation Analysis and Support, National Institute for Occupational
Safety and Health (NIOSH), 4676 Columbia Parkway, MS C-46, Cincinnati,
OH 45226, Telephone 513-533-6800 (this is not a toll-free number).
Information requests can also be submitted by e-mail to OCAS@CDC.GOV.
Christine M. Branche,
Acting Director, National Institute for Occupational Safety and
Health.
[FR Doc. E9-20899 Filed 8-28-09; 8:45 am]
BILLING CODE 4163-19-P