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    <RIN_INFO>
        <RIN>0910-AF55</RIN>
        <PUBLICATION>
            <PUBLICATION_ID>200504</PUBLICATION_ID>
            <PUBLICATION_TITLE>Unified Agenda of Federal Regulatory and Deregulatory Actions</PUBLICATION_TITLE>
        </PUBLICATION>
        <AGENCY>
            <CODE>0910</CODE>
            <NAME>Food and Drug Administration</NAME>
            <ACRONYM>FDA</ACRONYM>
        </AGENCY>
        <PARENT_AGENCY>
            <CODE>0900</CODE>
            <NAME>Department of Health and Human Services</NAME>
            <ACRONYM>HHS</ACRONYM>
        </PARENT_AGENCY>
        <RULE_TITLE>Requirements for Human and Animal Medical Products Manufactured From, Processed With, or Otherwise Containing Material From Cattle</RULE_TITLE>
        <ABSTRACT><![CDATA[This is a companion rulemaking to FDAs rule entitled "Use of Materials Derived From Cattle in Human and Animal Medical Products," to be published in the same issue of the Federal Register. The rule would propose recordkeeping requirements for human and animal medical products that contain cattle material. Manufacturers and sponsors of such products would have to establish and maintain records to demonstrate that prohibited materials were not used in their manufacture.]]></ABSTRACT>
        <PRIORITY_CATEGORY>Other Significant</PRIORITY_CATEGORY>
        <RIN_STATUS>Previously Published in The Unified Agenda</RIN_STATUS>
        <RULE_STAGE>Completed Actions</RULE_STAGE>
        <MAJOR>No</MAJOR>
        <UNFUNDED_MANDATE_LIST>
            <UNFUNDED_MANDATE>No</UNFUNDED_MANDATE>
        </UNFUNDED_MANDATE_LIST>
        <CFR_LIST>
            <CFR>21 CFR 116</CFR>
            <CFR>21 CFR 226.60</CFR>
            <CFR>21 CFR 300.200</CFR>
            <CFR>21 CFR 500</CFR>
            <CFR>21 CFR 600.16</CFR>
            <CFR>21 CFR 895</CFR>
            <CFR>21 CFR 1271.465</CFR>
            <CFR>21 CFR 1271.470</CFR>
        </CFR_LIST>
        <LEGAL_AUTHORITY_LIST>
            <LEGAL_AUTHORITY>Not Yet Determined</LEGAL_AUTHORITY>
        </LEGAL_AUTHORITY_LIST>
        <LEGAL_DLINE_LIST/>
        <RPLAN_ENTRY>No</RPLAN_ENTRY>
        <TIMETABLE_LIST>
            <TIMETABLE>
                <TTBL_ACTION>Withdrawn</TTBL_ACTION>
                <TTBL_DATE>03/11/2005</TTBL_DATE>
            </TIMETABLE>
        </TIMETABLE_LIST>
        <RFA_REQUIRED>No</RFA_REQUIRED>
        <SMALL_ENTITY_LIST>
            <SMALL_ENTITY>No</SMALL_ENTITY>
        </SMALL_ENTITY_LIST>
        <GOVT_LEVEL_LIST>
            <GOVT_LEVEL>None</GOVT_LEVEL>
        </GOVT_LEVEL_LIST>
        <FEDERALISM>Undetermined</FEDERALISM>
        <PRINT_PAPER>NA</PRINT_PAPER>
        <INTERNATIONAL_INTEREST>Not Collected</INTERNATIONAL_INTEREST>
        <RELATED_RIN_LIST>
            <RELATED_RIN>
                <RIN>0910-AF54</RIN>
                <RIN_RELATION>Merged with</RIN_RELATION>
            </RELATED_RIN>
        </RELATED_RIN_LIST>
        <AGENCY_CONTACT_LIST>
            <CONTACT>
                <FIRST_NAME>Eric</FIRST_NAME>
                <LAST_NAME>Flamm</LAST_NAME>
                <TITLE>Senior Policy Advisor, Office of Policy</TITLE>
                <AGENCY>
                    <CODE>0910</CODE>
                    <NAME>Food and Drug Administration</NAME>
                    <ACRONYM>FDA</ACRONYM>
                </AGENCY>
                <PHONE>301 796-4726</PHONE>
                <FAX>301 847-3541</FAX>
                <EMAIL>eric.flamm@fda.hhs.gov</EMAIL>
                <MAILING_ADDRESS>
                    <STREET_ADDRESS>Office of the Commissioner, WO1, Room 4315B, 10903 New Hampshire Ave.,</STREET_ADDRESS>
                    <CITY>Silver Spring</CITY>
                    <STATE>MD</STATE>
                    <ZIP>20993</ZIP>
                </MAILING_ADDRESS>
            </CONTACT>
        </AGENCY_CONTACT_LIST>
    </RIN_INFO>
</REGINFO_RIN_DATA>
