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CRE Letter to Director of NIEHS
January 28, 1999
Dr. Kenneth Olden I am writing to you in your capacity as the Secretary's principal advisor for the Report on Carcinogens Program to recommend, on behalf of the Center for Regulatory Effectiveness1, that a broad issue which goes to the heart of the purpose of the Program be brought before the NTP Executive Committee at its next meeting, and that the issue also be addressed by you and the Secretary in making final decisions on the contents of the upcoming 9th Report on Carcinogens. The issue, and several options for addressing it, are discussed in some detail in the attached paper. Two specific examples of agents under review for the upcoming 9th Report on Carcinogens which present the issue are discussed: tamoxifen and alcoholic beverages. The issue is basically this:
The attached paper points out that there is recent Federal legislation and expressions of Congressional policy concerning the importance of this issue and the need to address it through appropriate guidance. While such guidance is being considered by OMB and individual agencies, the Department of Health and Human Services is faced with having to move ahead to finalize the 9th Report on Carcinogens. Therefore, we have proposed some specific options for handling this matter in the 9th Report. These options are both short-term and long-term. Utilizing the special "Reviewed But Not Listed" appendix recommended for boot and shoe manufacturing in the 9th Report, or deferral, for example, are short-term methods of addressing the issue; but a long-term approach should consider public and OMB input and the option of setting up a special "Qualified Listings" category for certain substances for which additional listing information is necessary to avoid public confusion and potential detriment to public health.
We are taking the liberty of distributing this letter to members of the NTP Executive Committee. We are also providing it to members of the RoC Subcommittee of the NTP Board of Scientific Counselors and the Board in case you might also wish to seek their views on this subject. We also recommend consultation with OMB's Office of Information and Regulatory Affairs. We would be pleased to discuss this further at your convenience. Assuming the issue is brought before the Executive Committee, we would appreciate being informed of the action taken. Sincerely,
William G. Kelly, Jr.
1 The Center for Regulatory Effectiveness is a consortium of trade associations and companies, with a local government advisory panel, that was established several years ago to develop recommendations for Congress and Federal agencies on ways to improve the implementation of Federal programs, with particular emphasis on issues that involve multiple agencies.
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