Browse: Departments Dates Agencies
SUBJECT CATEGORY: National Toxicology Program (NTP); Center for the Evaluation of Risks to Human Reproduction (CERHR); Availability of the Draft Expert Panel Report on Bisphenol A and Request for Public Comment on the Draft Report; Announcement of the Bisphenol A Expert Panel Meeting
DOCUMENT SUMMARY: The CERHR announces the availability of the draft expert panel report for bisphenol A on December 15, 2006, from the CERHR Web site (http://cerhr.niehs.nih.gov) or in printed text from CERHR (see FOR FURTHER INFORMATION CONTACT below). The CERHR invites the submission of public comments on sections 14 of the draft expert panel report (see SUPPLEMENTARY INFORMATION below). The expert panel will meet on March 57, 2007, at the Radisson Hotel Old Town in Alexandria, Virginia to review and revise the draft expert panel report and reach conclusions regarding whether exposure to bisphenol A is a hazard to human development or reproduction. The expert panel will also identify data gaps and research needs. CERHR expert panel meetings are open to the public with time scheduled for oral public comment. Attendance is limited only by the available meeting room space. Following the expert panel meeting and completion of the expert panel report, the CERHR will post the final report on its Web site and solicit public comment on it through a Federal Register notice.
SUMMARY: National Toxicology Program—; Bisphenol A; expert panel report availability and comment,
Bisphenol A (CAS RN: 80507) is a high production volume chemical used in the production of epoxy resins, polyester resins, polysulfone resins, polyacrylate resins, polycarbonate plastics, and flame retardants. Polycarbonate plastics are used in food and drink packaging; resins are used as lacquers to coat metal products such as food cans, bottle tops, and water supply pipes. Some polymers used in dental sealants and tooth coatings contain bisphenol A. Exposure to the general population can occur through direct contact to bisphenol A or by exposure to food or drink that has been in contact with a material containing bisphenol A. CERHR selected this chemical for evaluation because of (1) high production volume, (2) widespread human exposure, (3) evidence of reproductive toxicity in laboratory animal studies, and (4) public concern.
At the meeting, the expert panel will review and revise the draft
expert panel report and reach conclusions regarding whether exposure to
bisphenol A is a hazard to human reproduction or development. Each draft expert panel report has the following sections:
1.0 Chemistry, Use, and Human Exposure.
2.0 General Toxicological and Biological Effects.
3.0 Developmental Toxicity Data.
4.0 Reproductive Toxicity Data.
5.0 Summary, Conclusions, and Critical Data Needs (to be prepared at expert panel meeting).
The CERHR invites written public comments on sections 14 of the draft expert panel report on bisphenol A. Any comments received will be posted on the CERHR website prior to the meeting and distributed to the expert panel and CERHR staff for their consideration in revising the draft report and/or preparing for the expert panel meeting. Persons submitting written comments are asked to include their name and contact information (affiliation, mailing address, telephone and facsimile numbers, email, and sponsoring organization, if any) and send them to Dr. Shelby (see ADDRESSES above) for receipt by February 2, 2007.
Time is setaside on March 5, 2007, for the presentation of oral public comments at the expert panel meeting. Seven minutes will be available for each speaker (one speaker per organization). When registering to comment orally, please provide your name, affiliation, mailing address, telephone and facsimile numbers, email and sponsoring organization (if any). If possible, send a copy of the statement or talking points to Dr. Shelby by February 2. This statement will be provided to the expert panel to assist them in identifying issues for discussion and will be noted in the meeting record. Registration for presentation of oral comments will also be available at the meeting on March 5, 2007, from 7:308:30 a.m. Persons registering at the meeting are asked to bring 20 copies of their statement or talking points for distribution to the expert panel and for the record.
The meeting begins each day at 8:30 a.m. On March 5 and 6, it is
anticipated that a lunch break will occur from noon1 p.m. and the
meeting will adjourn at 56 p.m. The meeting is expected to adjourn by
noon on March 7; however, adjournment may occur earlier or later
depending upon the time needed by the expert panel to complete its
work. Anticipated agenda topics for each day are listed below. March 5, 2007
The CERHR expert panel is composed of independent scientists
selected for their scientific expertise in reproductive and/or
developmental toxicology and other areas of science relevant for these evaluations.
Robert E. Chapin, PhD (Chair).......... Pfizer Inc., Groton, CT.
Jane Adams, PhD........................ University of Massachusetts, Boston, MA.
Kim Boekelheide, MD, PhD............... Brown University, Providence, RI.
Michael A. Gallo, PhD.................. University of Medicine &
Dentistry NJ, Piscataway, NJ.
Leon Earl Gray, Jr, PhD................ U.S. Environmental Protection
Agency, Research Triangle Park, NC.
Simon William Hayward, PhD............. Vanderbilt University Medical
Center, Nashville, TN.
Peter S.J. Lees, PhD................... The Johns Hopkins University, Baltimore, MD.
Barry S. McIntyre, PhD................. ScheringPlough Research
Institute, Summit, NJ.
Michael John McPhaul, MD............... The University of Texas, Dallas, Texas.
Kenneth Portier, PhD................... American Cancer Society, Atlanta, GA.
Teresa Schnorr, PhD.................... Centers for Disease Control,
National Institute for
Occupational Safety & Health, Cincinnati, OH.
Sherry G. Selevan, PhD................. Retired, U.S. Public Health
Service, Silver Spring, MD.
John G. Vandenbergh, PhD............... North Carolina State
University, Raleigh, NC.
Kendall B. Wallace, PhD................ University of Minnesota, Duluth, MN.
[[Page 74536]]
Susan R. Woskie, PhD................... University of Massachusetts
Lowell, Lowell, MA. Background Information on the CERHR
The NTP established CERHR in June 1998 [Federal Register, December 14, 1998 (Volume 63, Number 239, page 68782)]. CERHR is a publicly accessible resource for information about adverse reproductive and/or developmental health effects associated with exposure to environmental and/or occupational exposures. Expert panels conduct scientific evaluations of agents selected by the CERHR in public forums.
CERHR invites the nomination of agents for review or scientists for its expert registry. Information about CERHR and the nomination process can be obtained from its homepage (http://cerhr.niehs.nih.gov) or by contacting Dr. Shelby (see FOR FURTHER INFORMATION CONTACT above). CERHR selects chemicals for evaluation based upon several factors including production volume, potential for human exposure from use and occurrence in the environment, extent of public concern, and extent of data from reproductive and developmental toxicity studies.
CERHR follows a formal, multistep process for review and
evaluation of selected chemicals. The formal evaluation process was
published in the Federal Register on July 16, 2001 (Volume 66, Number
136, pages 3704737048) and is available on the CERHR Web site under ``About CERHR'' or in printed copy from CERHR.
Dated: November 27, 2006.
Samuel H. Wilson,
Deputy Director, National Institute of Environmental Health Sciences and National Toxicology Program.
[FR Doc. E621040 Filed 121106; 8:45 am]
BILLING CODE 414001P
FOR FURTHER INFORMATION CONTACT Dr. Michael D. Shelby, CERHR Director, 9195413455, shelby@niehs.nih.gov.
14 CFR Part 39 40 CFR Part 52 14 CFR Part 71 33 CFR Part 165 50 CFR Part 679 47 CFR Part 73 26 CFR Part 1 40 CFR Part 180 33 CFR Part 117 50 CFR Part 17 44 CFR Part 67 50 CFR Part 648 14 CFR Part 97 33 CFR Part 100 40 CFR Part 63 50 CFR Part 622 44 CFR Part 65 50 CFR Part 660 26 CFR Part 301 39 CFR Part 111 40 CFR Part 300 6 CFR Part 5 40 CFR Part 271 47 CFR Part 64 40 CFR Parts 52 and 81 44 CFR Part 64 10 CFR Part 50 49 CFR Part 571 50 CFR Part 665 47 CFR Part 76