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    <title>The Federal Register</title>
    <link>http://thefederalregister.com/b.p/department/DEPARTMENT_OF_JUSTICE/2003-11-25/</link>
    <description>Daily Publications of Meetings and Rules Changes for the Federal Government</description>
    <pubDate>Mon, May 20 2013 11:00:00 GMT</pubDate>
    <lastBuildDate>Mon, May 20 2013 11:00:00 GMT</lastBuildDate>
    <webMaster>info@thefederalregister.com</webMaster>
    <item>
  <title><![CDATA[  Chemical Registration Waivers; Exemption From Chemical  Registration Fees for Certain Persons]]></title>
  <link>http://thefederalregister.com/d.p/2003-11-25-03-29236</link>
  <description><![CDATA[ DEA is proposing amending its regulations to waive the 
requirement of registration for contract processors, medical/first aid 
kit providers, distributors of sample packages of drug products, and 
distributors of research/reference standards pursuant to 21 U.S.C. 
822(d). These actions are being taken in response to industry comments 
and suggestions. DEA has determined that requiring registration for 
these activities is not necessary for effective enforcement under the 
Controlled Substances Act (CSA), and waiving the requirement of 
registration will ease regulatory burdens for the affected industries. 
DEA is also proposing exempting charitable organizations and 
governmental entities from initial and renewal registration fees. These 
fee exemptions will bring the chemical regulations into conformance 
with the controlled substances regulations (21 CFR 1301.21).
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  <guid>http://thefederalregister.com/d.p/2003-11-25-03-29236</guid>
  <pubDate>Tue, Nov 25 2003 11:00:00 GMT</pubDate>
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<item>
  <title><![CDATA[  Recordkeeping and Reporting Requirements for Drug Products  Containing Gamma-Hydroxybutyric Acid (GHB)]]></title>
  <link>http://thefederalregister.com/d.p/2003-11-25-03-29336</link>
  <description><![CDATA[ DEA proposes to amend its regulations to require additional 
recordkeeping and reporting requirements for drug products containing 
gammahydroxybutyric acid (GHB) for which an application has been 
approved under the Federal Food, Drug, and Cosmetic Act. DEA proposes [[Page 66049]]<br/>
these changes pursuant to section 4 of the ``Hillory J. Farias and 
Samantha Reid DateRape Drug Prohibition Act of 2000.'' These 
additional requirements are necessary to protect against the diversion 
of GHB for illicit purposes.
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  <guid>http://thefederalregister.com/d.p/2003-11-25-03-29336</guid>
  <pubDate>Tue, Nov 25 2003 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  Agency Information Collection Activities: Proposed Collection;  Comments Requested]]></title>
  <link>http://thefederalregister.com/d.p/2003-11-25-03-29358</link>
  <description><![CDATA[
</p><p>    The Department of Justice (DOJ), Federal Bureau of Investigations 
(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 68, Number 150, 
page 46227 on August 5, 2003, allowing for a 60 day comment period.
</p><p>    The purpose of this notice is to allow for an additional 30 days 
for public comment until December 26, 2003. This process is conducted  in accordance with 5 CFR 1320.10.</p><p>    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 D<script type="text/javascript">
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  <guid>http://thefederalregister.com/d.p/2003-11-25-03-29358</guid>
  <pubDate>Tue, Nov 25 2003 11:00:00 GMT</pubDate>
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