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  <titleInfo>
    <title>Good manufacturing practices for pharmaceuticals</title>
    <subTitle>a plan for total quality control from manufacturer to consumer</subTitle>
  </titleInfo>
  <name type="personal">
    <namePart>Willig, Sidney H.</namePart>
    <namePart type="date">1919-</namePart>
    <role>
      <roleTerm authority="marcrelator" type="text">creator</roleTerm>
    </role>
  </name>
  <typeOfResource>text</typeOfResource>
  <genre authority="marc">bibliography</genre>
  <originInfo>
    <place>
      <placeTerm type="code" authority="marccountry">nyu</placeTerm>
    </place>
    <place>
      <placeTerm type="text">New York</placeTerm>
    </place>
    <publisher>M. Dekker</publisher>
    <dateIssued>c2001. [Reprinted 2005]</dateIssued>
    <dateIssued encoding="marc">2005</dateIssued>
    <edition>Fifth edition, rev. and expanded.</edition>
    <issuance>monographic</issuance>
  </originInfo>
  <language>
    <languageTerm authority="iso639-2b" type="code">eng</languageTerm>
  </language>
  <physicalDescription>
    <form authority="marcform">print</form>
    <extent>xii, 732 pages : illustrations ; 24 cm.</extent>
  </physicalDescription>
  <note type="statement of responsibility">Sidney H. Willig.</note>
  <note>Includes bibliographical references and index.</note>
  <subject authority="lcsh">
    <topic>Pharmaceutical industry</topic>
    <topic>Quality control</topic>
  </subject>
  <subject authority="lcsh">
    <topic>Drugs</topic>
    <topic>Standards</topic>
    <geographic>United States</geographic>
  </subject>
  <subject authority="mesh">
    <topic>Pharmaceutical Preparations</topic>
    <topic>standards</topic>
    <geographic>United States</geographic>
  </subject>
  <subject authority="mesh">
    <topic>Drug Industry</topic>
    <topic>standards</topic>
    <geographic>United States</geographic>
  </subject>
  <subject authority="mesh">
    <topic>Legislation, Drug</topic>
    <geographic>United States</geographic>
  </subject>
  <subject authority="mesh">
    <topic>Quality Control</topic>
    <geographic>United States</geographic>
  </subject>
  <subject authority="mesh">
    <topic>Technology, Pharmaceutical</topic>
    <topic>standards</topic>
    <geographic>United States</geographic>
  </subject>
  <subject authority="mesh">
    <topic>Pharmacy</topic>
  </subject>
  <classification authority="lcc">RS189 .W57 2001</classification>
  <classification authority="lcc">RS189 .W57 2001</classification>
  <classification authority="ddc" edition="22">615.19</classification>
  <classification authority="nlm">W1 DR893B v.109 2001</classification>
  <classification authority="nlm">QV 771 W732g 2001</classification>
  <identifier type="isbn">0824704258 (alk. paper)</identifier>
  <identifier type="lccn">00060188</identifier>
  <recordInfo>
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    <recordCreationDate encoding="marc">130817</recordCreationDate>
    <recordChangeDate encoding="iso8601">20220105125913.0</recordChangeDate>
    <recordIdentifier source="BD-DhAAL">27406</recordIdentifier>
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