Medical Use of Byproduct Material-Amendments/Medical Event Definitions, 8830-8831 [E8-2777]

Download as PDF 8830 Federal Register / Vol. 73, No. 32 / Friday, February 15, 2008 / Proposed Rules rule would not impose any additional reporting or recordkeeping requirements on either small or large spearmint oil producers and handlers. As with all Federal marketing order programs, reports and forms are periodically reviewed to reduce information requirements and duplication by industry and public sector agencies. The AMS is committed to complying with the E-Government Act, to promote the use of the Internet and other information technologies to provide increased opportunities for citizen access to Government information and services, and for other purposes. USDA has not identified any relevant Federal rules that duplicate, overlap, or conflict with this rule. In addition, the Committee’s meeting was widely publicized throughout the spearmint oil industry and all interested persons were invited to attend the meeting and participate in Committee deliberations on all issues. Like all Committee meetings, the October 17, 2007, meeting was a public meeting and all entities, both large and small, were able to express views on this issue. Finally, interested persons are invited to submit information on the regulatory and informational impacts of this action on small businesses. A small business guide on complying with fruit, vegetable, and specialty crop marketing agreements and orders may be viewed at: https://www.ams.usda.gov/ fv/moab.html. Any questions about the compliance guide should be sent to Jay Guerber at the previously mentioned address in the FOR FURTHER INFORMATION CONTACT section. A 30-day comment period is provided to allow interested persons the opportunity to respond to this proposal. This comment period is deemed appropriate so a final determination might be made prior to June 1, 2008, the beginning of the 2008–2009 marketing year. All written comments timely received will be considered before a final determination is made on this matter. List of Subjects in 7 CFR Part 985 rwilkins on PROD1PC63 with PROPOSALS Marketing agreements, Oils and fats, Reporting and recordkeeping requirements, Spearmint oil. For the reasons set forth in the preamble, 7 CFR part 985 is proposed to be amended as follows: PART 985—MARKETING ORDER REGULATING THE HANDLING OF SPEARMINT OIL PRODUCED IN THE FAR WEST 1. The authority citation for 7 CFR part 985 continues to read as follows: VerDate Aug<31>2005 17:07 Feb 14, 2008 Jkt 214001 Authority: 7 U.S.C. 601–674. 2. A new § 985.227 is added to read as follows: [Note: This section will not appear in the Code of Federal Regulations.] § 985.227 Salable quantities and allotment percentages—2008–2009 marketing year. The salable quantity and allotment percentage for each class of spearmint oil during the marketing year beginning on June 1, 2008, shall be as follows: (a) Class 1 (Scotch) oil—a salable quantity of 993,067 pounds and an allotment percentage of 50 percent. (b) Class 3 (Native) oil—a salable quantity of 1,184,748 pounds and an allotment percentage of 53 percent. Dated: February 12, 2008. Lloyd C. Day, Administrator, Agricultural Marketing Service. [FR Doc. E8–2922 Filed 2–14–08; 8:45 am] BILLING CODE 3410–02–P NUCLEAR REGULATORY COMMISSION 10 CFR Part 35 RIN 3150–AI26 [NRC–2008–0071] Medical Use of Byproduct Material— Amendments/Medical Event Definitions Nuclear Regulatory Commission. ACTION: Advance notice of proposed rulemaking. AGENCY: SUMMARY: The Nuclear Regulatory Commission (NRC) is making available preliminary draft rule language to amend its regulations concerning medical use of byproduct material. The goal of this rulemaking is to better define medical events arising from permanent implant brachytherapy procedures. The proposed amendments will change the criteria for defining a medical event for permanent implant brachytherapy from dose based to activity based, will add a requirement to report as a medical event any administration requiring a written directive if a written directive was not prepared, and will make certain administrative and clarification changes. The availability of the preliminary draft rule language is intended to inform stakeholders of the current status of the NRC’s activities and solicit public comments on the information at this time. Comments may be provided as indicated under the PO 00000 Frm 00006 Fmt 4702 Sfmt 4702 ADDRESSES heading. The NRC may post updates periodically under Docket # NRC–2008–0071 on the Federal eRulemaking Portal at https:// www.regulations.gov that may be of interest to stakeholders. DATES: Submit comments by February 26, 2008. Comments received after this date will be considered if it is practical to do so, but the NRC is able to assure consideration only for comments received on or before this date. ADDRESSES: Please include the following number RIN 3150–AI26 in the subject line of your comments. Comments on rulemakings submitted in writing or in electronic form will be made available to the public in their entirety on the NRC’s Web site in the Agencywide Documents Access and Management System (ADAMS) and on regulations.gov. Personal information, such as your name, address, telephone number, e-mail address, etc., will not be removed from your submission. You may submit comments by any one of the following methods. Electronically: Via the Federal eRulemaking Portal (Docket # NRC– 2008–0071) and follow instructions for submitting comments. Address questions about this docket to Carol Gallagher 301–415–5905; e-mail cag@nrc.gov. Mail comments to: Secretary, U.S. Nuclear Regulatory Commission, Washington, DC 20555–0001, ATTN: Rulemakings and Adjudications Staff. E-mail comments to: Rulemaking.Comments@nrc.gov. If you do not receive a reply e-mail confirming that we have received your comments, contact us directly at 301–415–1966. Hand deliver comments to: 11555 Rockville Pike, Rockville, Maryland 20852, between 7:30 a.m. and 4:15 p.m. Federal workdays. (Telephone 301–415– 1966). Fax comments to: Secretary, U.S. Nuclear Regulatory Commission at 301– 415–1101. Publicly available documents related to this rulemaking may be viewed electronically on the public computers located at the NRC’s Public Document Room (PDR), O1 F21, One White Flint North, 11555 Rockville Pike, Rockville, Maryland. The PDR reproduction contractor will copy documents for a fee. Publicly available documents created or received at the NRC after November 1, 1999, are available electronically at the NRC’s Electronic Reading Room at https://www.nrc.gov/reading-rm/ adams.html. From this site, the public can gain entry into ADAMS, which provides text and image files of NRC’s E:\FR\FM\15FEP1.SGM 15FEP1 Federal Register / Vol. 73, No. 32 / Friday, February 15, 2008 / Proposed Rules public documents. If you do not have access to ADAMS or if there are problems in accessing the documents located in ADAMS, contact the PDR Reference staff at 1–800–397–4209, 301– 415–4737 or by e-mail to pdr@nrc.gov. FOR FURTHER INFORMATION CONTACT: Edward M. Lohr, Office of Federal and State Materials and Environmental Management Programs, U.S. Nuclear Regulatory Commission, Washington, DC 20555–0001, telephone (301) 415– 0253, e-mail, eml1@nrc.gov. The preliminary draft rule language can be viewed and downloaded electronically via the Federal eRulemaking Portal at https://www.regulations.gov by searching for Docket # NRC–2008–0071 as well as in ADAMS (ML080350090). The goal of this rulemaking is to better define medical events arising from permanent implant brachytherapy procedures. The proposed amendments will change the criteria for defining a medical event for permanent implant brachytherapy from dose based to activity based, will add a requirement to report as a medical event any administration requiring a written directive if a written directive was not prepared, and will make certain administrative and clarification changes. The NRC is making a preliminary version of the draft proposed rule language available to inform stakeholders of the current status of this proposed rulemaking. This preliminary draft rule language may be subject to significant revisions during the rulemaking process. NRC is inviting stakeholders to comment on the draft revisions. The NRC may post updates to the draft proposed rule language on the Federal eRulemaking Portal. Stakeholders will also have an opportunity to comment on the rule language when it is published as a proposed rule. rwilkins on PROD1PC63 with PROPOSALS SUPPLEMENTARY INFORMATION: Dated at Rockville, Maryland, this 8th day of February, 2008. For the Nuclear Regulatory Commission. Dennis K. Rathbun, Director, Division of Intergovernmental Liaison and Rulemaking, Office of Federal and State Materials and Environmental Management Programs. [FR Doc. E8–2777 Filed 2–14–08; 8:45 am] BILLING CODE 7590–01–P VerDate Aug<31>2005 17:07 Feb 14, 2008 Jkt 214001 DEPARTMENT OF TRANSPORTATION 8831 (telephone (800) 647–5527) is in the section. Comments will be available in the AD docket shortly after receipt. ADDRESSES Federal Aviation Administration 14 CFR Part 39 RIN 2120–AA64 Airworthiness Directives; Pacific Aerospace Limited Model 750XL Airplanes Federal Aviation Administration (FAA), Department of Transportation (DOT). ACTION: Notice of proposed rulemaking (NPRM). AGENCY: SUMMARY: We propose to adopt a new airworthiness directive (AD) for the products listed above. This proposed AD results from mandatory continuing airworthiness information (MCAI) originated by an aviation authority of another country to identify and correct an unsafe condition on an aviation product. The MCAI describes the unsafe condition as: To prevent electrical malfunction from causing damage to the wiring that may result in arcing or fire, accomplish Pacific Aerospace Service Bulletin PACSB/XL/008. The proposed AD would require actions that are intended to address the unsafe condition described in the MCAI. DATES: We must receive comments on this proposed AD by March 17, 2008. ADDRESSES: You may send comments by any of the following methods: • Federal eRulemaking Portal: Go to https://www.regulations.gov. Follow the instructions for submitting comments. • Fax: (202) 493–2251. • Mail: U.S. Department of Transportation, Docket Operations, M– 30, West Building Ground Floor, Room W12–140, 1200 New Jersey Avenue, SE., Washington, DC 20590. • Hand Delivery: U.S. Department of Transportation, Docket Operations, M– 30, West Building Ground Floor, Room W12–140, 1200 New Jersey Avenue, SE., Washington, DC 20590, between 9 a.m. and 5 p.m., Monday through Friday, except Federal holidays. Examining the AD Docket You may examine the AD docket on the Internet at https:// www.regulations.gov; or in person at the Docket Management Facility between 9 a.m. and 5 p.m., Monday through Friday, except Federal holidays. The AD docket contains this proposed AD, the regulatory evaluation, any comments received, and other information. The street address for the Docket Office PO 00000 Frm 00007 Fmt 4702 Karl Schletzbaum, Aerospace Engineer, FAA, Small Airplane Directorate, 901 Locust, Room 301, Kansas City, Missouri 64106; telephone: (816) 329–4146; fax: (816) 329–4090. FOR FURTHER INFORMATION CONTACT: [Docket No. FAA–2008–0175; Directorate Identifier 2007–CE–105–AD] Sfmt 4702 SUPPLEMENTARY INFORMATION: Comments Invited We invite you to send any written relevant data, views, or arguments about this proposed AD. Send your comments to an address listed under the ADDRESSES section. Include ‘‘Docket No. FAA–2008–0175, Directorate Identifier 2007–CE–105–AD’’ at the beginning of your comments. We specifically invite comments on the overall regulatory, economic, environmental, and energy aspects of this proposed AD. We will consider all comments received by the closing date and may amend this proposed AD because of those comments. We will post all comments we receive, without change, to https:// www.regulations.gov, including any personal information you provide. We will also post a report summarizing each substantive verbal contact we receive about this proposed AD. Discussion The Civil Aviation Authority of New Zealand (CAA), which is the aviation authority for New Zealand, has issued DCA/750XL/2, dated September 30, 2004 (referred to after this as ‘‘the MCAI’’), to correct an unsafe condition for the specified products. The MCAI states: To prevent electrical malfunction from causing damage to the wiring that may result in arcing or fire, accomplish Pacific Aerospace Service Bulletin PACSB/XL/008. The MCAI requires the addition and replacement of certain pitot heat sensor circuit breakers and the addition of a cooling fan circuit fuse. You may obtain further information by examining the MCAI in the AD docket. Relevant Service Information Pacific Aerospace Corporation Limited has issued Mandatory Service Bulletin PACSB/XL/008, dated July 8, 2004. The actions described in this service information are intended to correct the unsafe condition identified in the MCAI. E:\FR\FM\15FEP1.SGM 15FEP1

Agencies

[Federal Register Volume 73, Number 32 (Friday, February 15, 2008)]
[Proposed Rules]
[Pages 8830-8831]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E8-2777]


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NUCLEAR REGULATORY COMMISSION

10 CFR Part 35

RIN 3150-AI26
[NRC-2008-0071]


Medical Use of Byproduct Material--Amendments/Medical Event 
Definitions

AGENCY: Nuclear Regulatory Commission.

ACTION: Advance notice of proposed rulemaking.

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

SUMMARY: The Nuclear Regulatory Commission (NRC) is making available 
preliminary draft rule language to amend its regulations concerning 
medical use of byproduct material. The goal of this rulemaking is to 
better define medical events arising from permanent implant 
brachytherapy procedures. The proposed amendments will change the 
criteria for defining a medical event for permanent implant 
brachytherapy from dose based to activity based, will add a requirement 
to report as a medical event any administration requiring a written 
directive if a written directive was not prepared, and will make 
certain administrative and clarification changes. The availability of 
the preliminary draft rule language is intended to inform stakeholders 
of the current status of the NRC's activities and solicit public 
comments on the information at this time. Comments may be provided as 
indicated under the ADDRESSES heading. The NRC may post updates 
periodically under Docket  NRC-2008-0071 on the Federal 
eRulemaking Portal at https://www.regulations.gov that may be of 
interest to stakeholders.

DATES: Submit comments by February 26, 2008. Comments received after 
this date will be considered if it is practical to do so, but the NRC 
is able to assure consideration only for comments received on or before 
this date.

ADDRESSES: Please include the following number RIN 3150-AI26 in the 
subject line of your comments. Comments on rulemakings submitted in 
writing or in electronic form will be made available to the public in 
their entirety on the NRC's Web site in the Agencywide Documents Access 
and Management System (ADAMS) and on regulations.gov. Personal 
information, such as your name, address, telephone number, e-mail 
address, etc., will not be removed from your submission. You may submit 
comments by any one of the following methods.
    Electronically: Via the Federal eRulemaking Portal (Docket 
 NRC-2008-0071) and follow instructions for submitting 
comments. Address questions about this docket to Carol Gallagher 301-
415-5905; e-mail cag@nrc.gov.
    Mail comments to: Secretary, U.S. Nuclear Regulatory Commission, 
Washington, DC 20555-0001, ATTN: Rulemakings and Adjudications Staff.
    E-mail comments to: Rulemaking.Comments@nrc.gov. If you do not 
receive a reply e-mail confirming that we have received your comments, 
contact us directly at 301-415-1966.
    Hand deliver comments to: 11555 Rockville Pike, Rockville, Maryland 
20852, between 7:30 a.m. and 4:15 p.m. Federal workdays. (Telephone 
301-415-1966).
    Fax comments to: Secretary, U.S. Nuclear Regulatory Commission at 
301-415-1101.
    Publicly available documents related to this rulemaking may be 
viewed electronically on the public computers located at the NRC's 
Public Document Room (PDR), O1 F21, One White Flint North, 11555 
Rockville Pike, Rockville, Maryland. The PDR reproduction contractor 
will copy documents for a fee.
    Publicly available documents created or received at the NRC after 
November 1, 1999, are available electronically at the NRC's Electronic 
Reading Room at https://www.nrc.gov/reading-rm/adams.html. From this 
site, the public can gain entry into ADAMS, which provides text and 
image files of NRC's

[[Page 8831]]

public documents. If you do not have access to ADAMS or if there are 
problems in accessing the documents located in ADAMS, contact the PDR 
Reference staff at 1-800-397-4209, 301-415-4737 or by e-mail to 
pdr@nrc.gov.

FOR FURTHER INFORMATION CONTACT: Edward M. Lohr, Office of Federal and 
State Materials and Environmental Management Programs, U.S. Nuclear 
Regulatory Commission, Washington, DC 20555-0001, telephone (301) 415-
0253, e-mail, eml1@nrc.gov.

SUPPLEMENTARY INFORMATION: The preliminary draft rule language can be 
viewed and downloaded electronically via the Federal eRulemaking Portal 
at https://www.regulations.gov by searching for Docket  NRC-
2008-0071 as well as in ADAMS (ML080350090).
    The goal of this rulemaking is to better define medical events 
arising from permanent implant brachytherapy procedures. The proposed 
amendments will change the criteria for defining a medical event for 
permanent implant brachytherapy from dose based to activity based, will 
add a requirement to report as a medical event any administration 
requiring a written directive if a written directive was not prepared, 
and will make certain administrative and clarification changes.
    The NRC is making a preliminary version of the draft proposed rule 
language available to inform stakeholders of the current status of this 
proposed rulemaking. This preliminary draft rule language may be 
subject to significant revisions during the rulemaking process. NRC is 
inviting stakeholders to comment on the draft revisions. The NRC may 
post updates to the draft proposed rule language on the Federal 
eRulemaking Portal. Stakeholders will also have an opportunity to 
comment on the rule language when it is published as a proposed rule.

    Dated at Rockville, Maryland, this 8th day of February, 2008.

    For the Nuclear Regulatory Commission.
Dennis K. Rathbun,
Director, Division of Intergovernmental Liaison and Rulemaking, Office 
of Federal and State Materials and Environmental Management Programs.
 [FR Doc. E8-2777 Filed 2-14-08; 8:45 am]
BILLING CODE 7590-01-P
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