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JAN 111963 MEMORANDUM FOR: William J. Dircks Executive Director for Operations FROM: John G. Davis, Director Office of Nuclear Material Safety and Safeguards Robert B. Minogue, Director Office of Nuclear Regulatory Research
SUBJECT:
PROPOSED REVISION OF 10 CFR PART 35 Enclosed is a major revision to 10 CFR Part 35, " Human Use of Byproduct Material," and proposals for streamlining the medical licensing process. As indicated at a briefing on December 15, 1982, the proposed rule is expected to reduce paper work, decrease backlog, support regionalization, and facilitate computerized management of the review process. It is consistent with the Commission's FY 1983 through 1987 Policy and Planning Guidance. It is also a key step in our continuing effort to improve the materials licensing process.
It will not reduce safety requirements.
NRC offices affected by the paper's implementation concurred in its publication for public comment at this time. However, the Office of State Programs stated that several Agreement States were in favor of continuing the practice of having applicants submit specific radiation safety procedures to NRC for review and approval. This practice was deliberately excluded from the proposed revision for reasons detailed in the paper.
The Office of Policy Evaluation has been kept informed of the task force's progress, and has been sent copies of draft proposals as they have been completed.
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William J. Dircks 2 This-paper represents a major effort by the Office of Nuclear Material Safety and Safeguards and the Office of Nuclear Regulatory Research and is jointly sponsored by both.
N fJohnG. Davis, Director Office of Nuclear Material Safety
, and Safeguards
/[,.f,-) (h yt.c~ O Robert B. Minogue, Director Office of Nuclear Regulatory Research
Enclosure:
Proposed Revision of 10 CFR Part 35 I
, ,.r JAN 11 1993 MEMORANDUM FOR: William J. Dircks Executive Director for Operations FROM: John G. Davis, Director Office of Nuclear Material Safety and Safeguards Robert B. Minogue, Director Office of Nuclear Regulatory Research
SUBJECT:
PROPOSED REVISION OF 10 CFR PART 35 Enclosed is a major revision to 10 CFR Part 35, " Human Use of Byproduct Material," and proposals for streamlining the medical licensing process. As indicated at a briefing on December 15, 1982, the proposed rule is expected to reduce paper work, decrease backlog, support regionalization, and facilitate computerized management of the review process. It is consistent with the Commission's FY 1983 through 1987 Policy and Planning Guidance. It is also a key step in our continuing effort to improve the materials licensing process.
It will not red're safety requirements.
NRC offices affected by the paper's implementation concurred in its publication for public comment at this time. However, the Office of State Programs stated that several Agreement States were in favor of continuing the practice of having applicants submit specific radiation safety procedures to NRC for review and approval. This practice was deliberately excluded from the proposed revision for reasons detailed in the paper.
The Office of Policy Evaluation has been_kept informed of the task force's progress, and has been sent copies of draft proposals as they have been completed.
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William J. Dircks 2 UAN 11 G83 This paper represents a major effort by the Office of Nuclear Material Safety and Safeguards and the Office of Nuclear Regulatory Research and is jointly sponsored by both.
John G. Davis, Director Office of Nuclear Material Safety and Safeguards Oricia.cl 31Cnod byg ROEIRTB.I!EOGW j Robert B. Minogue, Director Office of Nuclear Regulatory Research
Enclosure:
Proposed Revision of 10 CFR Part 35 DISTRIBUTION NMSS #821090
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