<?xml version='1.0' encoding='utf-8'?>

<rss version="2.0">
  <channel>
    <title>The Federal Register</title>
    <link>http://thefederalregister.com/b.p/agency/Food_and_Drug_Administration/2003-12-08/</link>
    <description>Daily Publications of Meetings and Rules Changes for the Federal Government</description>
    <pubDate>Sun, Nov 23 2008 11:00:00 GMT</pubDate>
    <lastBuildDate>Sun, Nov 23 2008 11:00:00 GMT</lastBuildDate>
    <webMaster>info@thefederalregister.com</webMaster>
    <item>
  <title><![CDATA[  Agency Information Collection Activities: Proposed Collection;  Comment Request; Hazard Analysis and Critical Control]]></title>
  <link>http://thefederalregister.com/d.p/2003-12-08-03-30302</link>
  <description><![CDATA[ The Food and Drug Administration (FDA) is announcing an 
opportunity for public comment on the proposed collection of certain 
information by the agency. Under the Paperwork Reduction Act of 1995 
(the PRA), Federal agencies are required to publish notice in the 
Federal Register concerning each proposed collection of information, 
including each proposed extension of an existing collection of 
information, and to allow 60 days for public comment in response to the 
notice. This notice solicits comments on recordkeeping requirements for 
applying hazard analysis and critical control point (HAACP) procedures 
for safe and sanitary processing for processors of fruit and vegetable 
juice.
<script type="text/javascript">
<!--
google_ad_client = "pub-2051746026283201";
google_ad_width = 728;
google_ad_height = 15;
google_ad_format = "728x15_0ads_al";
//2007-08-22: federalregister-rss
google_ad_channel = "2005962856";
google_color_border = "CC0000";
google_color_bg = "FFFFFF";
google_color_link = "CC0000";
google_color_text = "000000";
google_color_url = "008000";
//-->
</script>
<script type="text/javascript"
  src="http://pagead2.googlesyndication.com/pagead/show_ads.js">
</script>
]]></description>
  <guid>http://thefederalregister.com/d.p/2003-12-08-03-30302</guid>
  <pubDate>Mon, Dec 8 2003 11:00:00 GMT</pubDate>
</item>
<item>
  <title><![CDATA[  Amending the MedWatch Forms to Collect Postmarketing Adverse  Event Data Relating to Race and Ethnicity]]></title>
  <link>http://thefederalregister.com/d.p/2003-12-08-03-30300</link>
  <description><![CDATA[ The Food and Drug Administration (FDA) is requesting comment 
on the advantages and disadvantages of systematically collecting race 
and ethnicity data in postmarketing adverse event reports. FDA is also 
seeking feedback on whether FDA's MedWatch forms (Forms 3500 and 3500A) 
should be amended to collect the race and ethnicity data. If the 
MedWatch forms are amended to collect race and ethnicity data, FDA 
would like comment on how the forms should be amended and the financial 
impact of amending the forms on both voluntary and mandatory reporters. 
FDA is also asking for comment on the implications that collecting such 
race and ethnicity data would have for international reporting of 
postmarketing adverse events.
<script type="text/javascript">
<!--
google_ad_client = "pub-2051746026283201";
google_ad_width = 728;
google_ad_height = 15;
google_ad_format = "728x15_0ads_al";
//2007-08-22: federalregister-rss
google_ad_channel = "2005962856";
google_color_border = "CC0000";
google_color_bg = "FFFFFF";
google_color_link = "CC0000";
google_color_text = "000000";
google_color_url = "008000";
//-->
</script>
<script type="text/javascript"
  src="http://pagead2.googlesyndication.com/pagead/show_ads.js">
</script>
]]></description>
  <guid>http://thefederalregister.com/d.p/2003-12-08-03-30300</guid>
  <pubDate>Mon, Dec 8 2003 11:00:00 GMT</pubDate>
</item>
</channel>
</rss>

