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  <FDSYS>
    <CFRTITLE>21</CFRTITLE>
    <CFRTITLETEXT>Food and Drugs</CFRTITLETEXT>
    <VOL>1</VOL>
    <DATE>2003-04-01</DATE>
    <ORIGINALDATE>2003-04-01</ORIGINALDATE>
    <COVERONLY>false</COVERONLY>
    <TITLE>Testing facility management.</TITLE>
    <GRANULENUM>58.31</GRANULENUM>
    <HEADING>Section 58.31</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</PARENT>
      <PARENT HEADING="SUBCHAPTER A" SEQ="2">GENERAL</PARENT>
      <PARENT HEADING="PART 58" SEQ="1">GOOD LABORATORY PRACTICE FOR NONCLINICAL LABORATORY STUDIES</PARENT>
      <PARENT HEADING="Subpart B" SEQ="0">Organization and Personnel</PARENT>
    </ANCESTORS>
  </FDSYS>
  <SECTION>
    <SECTNO>§ 58.31</SECTNO>
    <SUBJECT>Testing facility management.</SUBJECT>
    <P>For each nonclinical laboratory study, testing facility management shall:</P>
    <P>(a) Designate a study director as described in § 58.33, before the study is initiated.</P>
    <P>(b) Replace the study director promptly if it becomes necessary to do so during the conduct of a study.</P>
    <P>(c) Assure that there is a quality assurance unit as described in § 58.35.</P>
    <P>(d) Assure that test and control articles or mixtures have been appropriately tested for identity, strength, purity, stability, and uniformity, as applicable.</P>
    <P>(e) Assure that personnel, resources, facilities, equipment, materials, and methodologies are available as scheduled.</P>
    <P>(f) Assure that personnel clearly understand the functions they are to perform.</P>
    <P>(g) Assure that any deviations from these regulations reported by the quality assurance unit are communicated to the study director and corrective actions are taken and documented.</P>
    <CITA>[43 FR 60013, Dec. 22, 1978, as amended at 52 FR 33780, Sept. 4, 1987]</CITA>
  </SECTION>
</CFRGRANULE>
