Agency Information Collection Activities: Proposed Collection; Comments Requested, 22703-22704 [05-8680]

Download as PDF Federal Register / Vol. 70, No. 83 / Monday, May 2, 2005 / Notices Country accounted for by your firm’s(s’) imports; (b) the quantity and value (f.o.b. U.S. port, including antidumping duties) of U.S. commercial shipments of Subject Merchandise imported from the Subject Country; and (c) the quantity and value (f.o.b. U.S. port, including antidumping duties) of U.S. internal consumption/company transfers of Subject Merchandise imported from the Subject Country. (9) If you are a producer, an exporter, or a trade/business association of producers or exporters of the Subject Merchandise in the Subject Country, provide the following information on your firm’s(s’) operations on that product during calendar year 2004 (report quantity data in pounds and value data in U.S. dollars, landed and duty-paid at the U.S. port but not including antidumping duties). If you are a trade/business association, provide the information, on an aggregate basis, for the firms which are members of your association. (a) Production (quantity) and, if known, an estimate of the percentage of total production of Subject Merchandise in the Subject Country accounted for by your firm’s(s’) production; and (b) the quantity and value of your firm’s(s’) exports to the United States of Subject Merchandise and, if known, an estimate of the percentage of total exports to the United States of Subject Merchandise from the Subject Country accounted for by your firm’s(s’) exports. (10) Identify significant changes, if any, in the supply and demand conditions or business cycle for the Domestic Like Product that have occurred in the United States or in the market for the Subject Merchandise in the Subject Country since the Order Date, and significant changes, if any, that are likely to occur within a reasonably foreseeable time. Supply conditions to consider include technology; production methods; development efforts; ability to increase production (including the shift of production facilities used for other products and the use, cost, or availability of major inputs into production); and factors related to the ability to shift supply among different national markets (including barriers to importation in foreign markets or changes in market demand abroad). Demand conditions to consider include end uses and applications; the existence and availability of substitute products; and the level of competition among the Domestic Like Product produced in the United States, Subject Merchandise produced in the Subject Country, and such merchandise from other countries. VerDate jul<14>2003 19:05 Apr 29, 2005 Jkt 205001 (11) (Optional) A statement of whether you agree with the above definitions of the Domestic Like Product and Domestic Industry; if you disagree with either or both of these definitions, please explain why and provide alternative definitions. Authority: This review is being conducted under authority of title VII of the Tariff Act of 1930; this notice is published pursuant to section 207.61 of the Commission’s rules. By order of the Commission. Issued: April 20, 2005. Marilyn R. Abbott, Secretary to the Commission. [FR Doc. 05–8722 Filed 4–29–05; 8:45 am] BILLING CODE 7020–02–P DEPARTMENT OF JUSTICE Drug Enforcement Administration Agency Information Collection Activities: Proposed Collection; Comments Requested ACTION: 60–Day emergency notice of information collection under review: National drug-related death reporting system. The Drug Enforcement Administration (DEA) has submitted the following information collection request to the Office of Management and Budget (OMB) for review and clearance in accordance with emergency review procedures of the Paperwork Reduction Act of 1995. OMB approval has been requested by DEA. The proposed information collection is published to obtain comments from the public and affected agencies. If granted, the emergency approval is only valid for 180 days. Comments should be directed to OMB, Office of Information and Regulatory Affairs, Attention: Department of Justice Desk Officer, Washington, DC 20503. Comments are encouraged and will be accepted until July 1, 2005. During the first 60 days of this same review period, a regular review of this information collection is also being undertaken. All comments and suggestions, or questions regarding additional information, to include obtaining a copy of the proposed information collection instrument with instructions, should be directed to Christine Sannerud, Ph.D., Chief, Drug and Chemical Evaluation Section, Office of Diversion Control, Drug Enforcement Administration, Washington, DC 20537. Written comments and suggestions from the public and affected agencies concerning the proposed collection of information are encouraged. Your PO 00000 Frm 00077 Fmt 4703 Sfmt 4703 22703 comments should address one or more of the following four points: • Evaluate whether the proposed collection of information is necessary for the proper performance of the functions of the agency, including whether the information will have practical utility; • Evaluate the accuracy of the agencies estimate of the burden of the proposed collection of information, including the validity of the methodology and assumptions used; • Enhance the quality, utility, and clarity of the information to be collected; and • Minimize the burden of the collection of information on those who are to respond, including through the use of appropriate automated, electronic, mechanical, or other technological collection techniques or other forms of information technology, e.g., permitting electronic submission of responses. Overview of this information: (1)Type of information collection: New collection. (2)The title of the form/collection: National Drug-Related Death Reporting System. (3)The agency form number, if any, and the applicable component of the department sponsoring the collection: Form Number: None. Office of Diversion Control, Drug Enforcement Administration, United States Department of Justice. (4) Affected public who will be asked or required to respond, as well as a brief abstract: Primary: State, local and tribal government. Other: None. The National Drug-Related Death Reporting System collects scientifically verified drugrelated death information from medical examiners’ and coroners’ offices that will be used to detect new and/or changing trends in drug abuse; provide local, regional, state and national trends of drug trafficking and abuse; provide information in support of drug scheduling actions; and better monitor the diversion of legitimately marketed drugs. (5) An estimate of the total number of respondents and the amount of time estimated for an average respondent to respond/reply: It is estimated that the NDDRS will contain approximately 30% of the 3200 offices providing data to the system via direct web submission or direct data extraction. Data extraction will be executed via a computer interface program and will require less than 5 minutes of the respondent’s time per month to complete. Data entry into the Web submission form is estimated to take 4 minutes per record, with a request for 50 records per month. E:\FR\FM\02MYN1.SGM 02MYN1 22704 Federal Register / Vol. 70, No. 83 / Monday, May 2, 2005 / Notices (6) An estimate of the total public burden (in hours) associated with the collection: The estimated total public burden associated with the Web submission form will be 19,200 hours annually, while bulk data extraction is estimated at 576 hours annually. If additional information is required contact: Brenda E. Dyer, Department Clearance Officer, United States Department of Justice, Justice Management Division, Policy and Planning Staff, Patrick Henry Building, Suite 1600, 601 D Street NW., Washington, DC 20530. Dated: April 25, 2005. William J. Walker, Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration. [FR Doc. 05–8694 Filed 4–29–05; 8:45 am] Dated: April 25, 2005. William J. Walker, Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration. [FR Doc. 05–8693 Filed 4–29–05; 8:45 am] BILLING CODE 4410–09–P BILLING CODE 4410–09–P Dated: April 27, 2005. Brenda E. Dyer, Department Clearance Officer, United States Department of Justice. [FR Doc. 05–8680 Filed 4–29–05; 8:45 am] Pursuant to Section 1301.33(a) of Title 21 of the Code of Federal Regulations (CFR), this is notice that on January 5, 2005, Roche Diagnostics Operations Inc., Attn: Regulatory Compliance, 9115 Hague Road, Indianapolis, Indiana 46250, made application by renewal to the Drug Enforcement Administration (DEA) to be registered as a bulk manufacturer of the basic classes of controlled substances listed in Schedules I and II: BILLING CODE 4410–09–P DEPARTMENT OF JUSTICE Drug Enforcement Administration Manufacturer of Controlled Substances; Notice of Application 19:05 Apr 29, 2005 Jkt 205001 Drug Enforcement Administration Manufacturer of Controlled Substances; Notice of Application Drug Pursuant to Section 1301.33(a) of Title 21 of the Code of Federal Regulations (CFR), this is notice that on February 18, 2005, Lilly Del Caribe, Inc., Chemical Plant, Kilometer 146.7, State Road 2, Mayaguez, Puerto Rico 00680, made application by renewal to the Drug Enforcement Administration (DEA) to be registered as a bulk manufacturer of Dextropropoxyphene (9273), a basic class of controlled substance listed in Schedules II. The company plans to manufacture the listed controlled substance in bulk for distribution to its customers. Any other such applicant and any person who is presently registered with DEA to manufacture such a substance may file comments or objections to the issuance of the proposed registration pursuant to 21 CFR 1301.33(a). Any such written comments or objections being sent via regular mail may be addressed, in quintuplicate, to the Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration, Washington, DC 20537, Attention: DEA Federal Register Representative, Liaison and Policy Section (ODL); or any being sent via express mail should be sent to DEA Headquarters, Attention: DEA Federal Register Representative/ODL, 2401 Jefferson-Davis Highway, Alexandria, Virginia 22301; and must be filed no later than July 1, 2005. VerDate jul<14>2003 DEPARTMENT OF JUSTICE DEPARTMENT OF JUSTICE Schedule Lysergic Acid Diethylamide (7315) Tetrahydrocannabinol (7370) ....... Alphamethadol (9605) .................. Phencyclidine (7471) .................... Benzoylecgonine (9180) ............... Methadone (9250) ........................ Morphine (9300) ........................... I I I II II II II The company plans to manufacture small quantities of the listed controlled substances for use in diagnostic products. Any other such applicant and any person who is presently registered with DEA to manufacture such a substance may file comments or objections to the issuance of the proposed registration pursuant to 21 CFR 1301.33(a). Any such written comments or objections being sent via regular mail may be addressed, in quintuplicate, to the Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration, Washington, DC 20537, Attention: DEA Federal Register Representative, Liaison and Policy Section (ODL); or any being sent via express mail should be sent to DEA Headquarters, Attention: DEA Federal Register Representative/ODL, 2401 Jefferson-Davis Highway, Alexandria, Virginia 22301; and must be filed no later than July 1, 2005. PO 00000 Frm 00078 Fmt 4703 Sfmt 4703 Federal Bureau of Investigation Agency Information Collection Activities: Proposed Collection; Comments Requested 30-Day Notice of Information Collection Under Review: Voluntary Appeal File (VAF) Brochure. ACTION: The Department of Justice (DOJ), Federal Bureau of Investigation (FBI) has submitted the following information collection request to the Office of Management and Budget (OMB) for review and approval in accordance with the Paperwork Reduction Act of 1995. The proposed information collection is published to obtain comments from the public and affected agencies. This proposed information collection was previously published in the Federal Register Volume 69, Number 218, page 65455 on November 12, 2004, allowing for a 60 day comment period. The purpose of this notice is to allow for an additional 30 days for public comment until June 1, 2005. This process is conducted in accordance with 5 CFR 1320.10. Written comments and/or suggestions regarding the items contained in this notice, especially the estimated public burden and associated response time, should be directed to the Office of Management and Budget, Office of Information and Regulatory Affairs, Attention Department of Justice Desk Officer, Washington, DC 20503. Additionally, comments may be submitted to OMB via facsimile to (202) 395–5806. Written comments and suggestions from the public and affected agencies concerning the proposed collection of information are encouraged. Your comments should address one or more of the following four points: —Evaluate whether the proposed collection of information is necessary for the proper performance of the functions of the agency, including whether the information will have practical utility; —Evaluate the accuracy of the agencies estimate of the burden of the proposed collection of information, including the validity of the methodology and assumptions used; E:\FR\FM\02MYN1.SGM 02MYN1

Agencies

[Federal Register Volume 70, Number 83 (Monday, May 2, 2005)]
[Notices]
[Pages 22703-22704]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 05-8680]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration


Agency Information Collection Activities: Proposed Collection; 
Comments Requested

ACTION: 60-Day emergency notice of information collection under review: 
National drug-related death reporting system.

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

    The Drug Enforcement Administration (DEA) has submitted the 
following information collection request to the Office of Management 
and Budget (OMB) for review and clearance in accordance with emergency 
review procedures of the Paperwork Reduction Act of 1995. OMB approval 
has been requested by DEA. The proposed information collection is 
published to obtain comments from the public and affected agencies. If 
granted, the emergency approval is only valid for 180 days. Comments 
should be directed to OMB, Office of Information and Regulatory 
Affairs, Attention: Department of Justice Desk Officer, Washington, DC 
20503. Comments are encouraged and will be accepted until July 1, 2005.
    During the first 60 days of this same review period, a regular 
review of this information collection is also being undertaken. All 
comments and suggestions, or questions regarding additional 
information, to include obtaining a copy of the proposed information 
collection instrument with instructions, should be directed to 
Christine Sannerud, Ph.D., Chief, Drug and Chemical Evaluation Section, 
Office of Diversion Control, Drug Enforcement Administration, 
Washington, DC 20537.
    Written comments and suggestions from the public and affected 
agencies concerning the proposed collection of information are 
encouraged. Your comments should address one or more of the following 
four points:
     Evaluate whether the proposed collection of information is 
necessary for the proper performance of the functions of the agency, 
including whether the information will have practical utility;
     Evaluate the accuracy of the agencies estimate of the 
burden of the proposed collection of information, including the 
validity of the methodology and assumptions used;
     Enhance the quality, utility, and clarity of the 
information to be collected; and
     Minimize the burden of the collection of information on 
those who are to respond, including through the use of appropriate 
automated, electronic, mechanical, or other technological collection 
techniques or other forms of information technology, e.g., permitting 
electronic submission of responses.
    Overview of this information:
    (1)Type of information collection: New collection.
    (2)The title of the form/collection: National Drug-Related Death 
Reporting System.
    (3)The agency form number, if any, and the applicable component of 
the department sponsoring the collection: Form Number: None. Office of 
Diversion Control, Drug Enforcement Administration, United States 
Department of Justice.
    (4) Affected public who will be asked or required to respond, as 
well as a brief abstract: Primary: State, local and tribal government. 
Other: None. The National Drug-Related Death Reporting System collects 
scientifically verified drug-related death information from medical 
examiners' and coroners' offices that will be used to detect new and/or 
changing trends in drug abuse; provide local, regional, state and 
national trends of drug trafficking and abuse; provide information in 
support of drug scheduling actions; and better monitor the diversion of 
legitimately marketed drugs.
    (5) An estimate of the total number of respondents and the amount 
of time estimated for an average respondent to respond/reply: It is 
estimated that the NDDRS will contain approximately 30% of the 3200 
offices providing data to the system via direct web submission or 
direct data extraction. Data extraction will be executed via a computer 
interface program and will require less than 5 minutes of the 
respondent's time per month to complete. Data entry into the Web 
submission form is estimated to take 4 minutes per record, with a 
request for 50 records per month.

[[Page 22704]]

    (6) An estimate of the total public burden (in hours) associated 
with the collection: The estimated total public burden associated with 
the Web submission form will be 19,200 hours annually, while bulk data 
extraction is estimated at 576 hours annually.
    If additional information is required contact: Brenda E. Dyer, 
Department Clearance Officer, United States Department of Justice, 
Justice Management Division, Policy and Planning Staff, Patrick Henry 
Building, Suite 1600, 601 D Street NW., Washington, DC 20530.

    Dated: April 27, 2005.
Brenda E. Dyer,
Department Clearance Officer, United States Department of Justice.
[FR Doc. 05-8680 Filed 4-29-05; 8:45 am]
BILLING CODE 4410-09-P

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