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Revision to 10 CFR 35 posted in the Federal Register



The following is the first part of the post.  The effective date is October

24, 2002.



To view the whole posting, go to

http://www.access.gpo.gov/su_docs/aces/aces140.html



Mark "Final Rules and Regulations"



for Issue date, make "ON" and enter 04/24/2002



For "Search Term" enter NRC



There are three sections.  



-- John 

John Jacobus, MS

Certified Health Physicist 

3050 Traymore Lane

Bowie, MD  20715-2024



E-mail:  jenday1@email.msn.com (H)      

--------------------------------------

[Federal Register: April 24, 2002 (Volume 67, Number 79)]

[Rules and Regulations]               

[Page 20249-20298]

>From the Federal Register Online via GPO Access [wais.access.gpo.gov]

[DOCID:fr24ap02-17]                         

 

[[Page 20249]]



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Part III



Nuclear Regulatory Commission

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10 CFR Parts 20, 32, and 35

Medical Use of Byproduct Material; Final Rule

[[Page 20250]]

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NUCLEAR REGULATORY COMMISSION



10 CFR Parts 20, 32, and 35



RIN 3150-AF74



Medical Use of Byproduct Material



AGENCY: Nuclear Regulatory Commission.



ACTION: Final rule.



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SUMMARY: The Nuclear Regulatory Commission (NRC) is amending its 

regulations regarding the medical use of byproduct material. This final 

rule is one component of the Commission's overall program for revising 

its regulatory framework for medical use. The overall goals of this 

program are to focus NRC's regulations on those medical procedures that 

pose the highest risk to workers, patients, and the public, and to 

structure its regulations to be more risk-informed and more 

performance-based, consistent with the NRC's ``Strategic Plan for 

Fiscal Year 1997-Fiscal Year 2002.''



EFFECTIVE DATE: This regulation becomes effective on October 24, 2002.



ADDRESSES: Documents related to this rulemaking may be examined at the 

NRC Public Document Room, One White Flint North, 11555 Rockville Pike, 

Room O-1 F23, Rockville, MD 20852. Available documents include the 

final environmental assessment, regulatory analysis, regulatory 

flexibility analysis, and NUREG-1556, Vol. 9(draft), ``Consolidated 

Guidance About Materials Licenses: Program Specific Guidance About 

Medical Use Licenses.'' Documents created or received at the NRC after 

November 1, 1999, are also available electronically at the NRC's Public 

Electronic Reading Room on the Internet at http://www.nrc.gov/reading-

rm.html. From this site, the public can gain entry into the NRC's 

Agencywide Document Access and Management System (ADAMS), which 

provides text and image files of NRC's public documents. For more 

information, contact the NRC Public Document Room (PDR) Reference staff 

at 1-800-397-4209, 301-415-4737 or by E-mail to pdr@nrc.gov.



FOR FURTHER INFORMATION CONTACT: Roger W. Broseus, Office of Nuclear 

Material Safety and Safeguards, Nuclear Regulatory Commission, 

Washington, DC 20555-0001, (301) 415-7608, E-mail RWB@nrc.gov.



SUPPLEMENTARY INFORMATION:

. . .

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