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    <FDSYS>
        <CFRTITLE>21</CFRTITLE>
        <CFRTITLETEXT>Food and Drugs</CFRTITLETEXT>
        <VOL>4</VOL>
        <DATE>2024-04-01</DATE>
        <ORIGINALDATE>2024-04-01</ORIGINALDATE>
        <COVERONLY>false</COVERONLY>
        <TITLE>Special testing requirements.</TITLE>
        <GRANULENUM>211.167</GRANULENUM>
        <HEADING>Section 211.167</HEADING>
        <ANCESTORS>
            <PARENT HEADING="Title 21" SEQ="4">Food and Drugs</PARENT>
            <PARENT HEADING="CHAPTER I" SEQ="3">FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED)</PARENT>
            <PARENT HEADING="SUBCHAPTER C" SEQ="2">DRUGS: GENERAL</PARENT>
            <PARENT HEADING="PART 211" SEQ="1">CURRENT GOOD MANUFACTURING PRACTICE FOR FINISHED PHARMACEUTICALS</PARENT>
            <PARENT HEADING="Subpart I" SEQ="0">Laboratory Controls</PARENT>
        </ANCESTORS>
    </FDSYS>
    <SECTION>
        <SECTNO>§ 211.167</SECTNO>
        <SUBJECT>Special testing requirements.</SUBJECT>
        <P>(a) For each batch of drug product purporting to be sterile and/or pyrogen-free, there shall be appropriate laboratory testing to determine conformance to such requirements. The test procedures shall be in writing and shall be followed.</P>
        <P>
            (b) For each batch of ophthalmic ointment, there shall be appropriate testing to determine conformance to specifications regarding the presence of foreign particles and harsh or abrasive 
            <PRTPAGE P="173"/>
            substances. The test procedures shall be in writing and shall be followed.
        </P>
        <P>(c) For each batch of controlled-release dosage form, there shall be appropriate laboratory testing to determine conformance to the specifications for the rate of release of each active ingredient. The test procedures shall be in writing and shall be followed.</P>
    </SECTION>
</CFRGRANULE>
