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  <titleInfo>
    <title>Good pharmaceutical manufacturing practice</title>
    <subTitle>rationale and compliance</subTitle>
  </titleInfo>
  <name type="personal">
    <namePart>Sharp, John</namePart>
    <role>
      <roleTerm authority="marcrelator" type="text">creator</roleTerm>
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  <typeOfResource>text</typeOfResource>
  <genre authority="marc">bibliography</genre>
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    <place>
      <placeTerm type="text">Boca Raton, Fla</placeTerm>
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    <publisher>CRC Press</publisher>
    <dateIssued>2019</dateIssued>
    <dateIssued encoding="marc">2005</dateIssued>
    <issuance>monographic</issuance>
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  <language>
    <languageTerm authority="iso639-2b" type="code">eng</languageTerm>
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  <physicalDescription>
    <form authority="marcform">print</form>
    <extent>ix, 503 p. : ill. ; 26 cm.</extent>
  </physicalDescription>
  <note type="statement of responsibility">by John Sharp</note>
  <subject authority="lcsh">
    <topic>Drugs</topic>
    <topic>Standards</topic>
    <geographic>United States</geographic>
  </subject>
  <subject authority="lcsh">
    <topic>Drugs</topic>
    <topic>Standards</topic>
    <geographic>European Union Countries</geographic>
  </subject>
  <subject authority="lcsh">
    <topic>Pharmaceutical industry</topic>
    <geographic>United States</geographic>
    <topic>Quality control</topic>
  </subject>
  <subject authority="lcsh">
    <topic>Pharmaceutical industry</topic>
    <geographic>European Union Countries</geographic>
    <topic>Quality control</topic>
  </subject>
  <subject authority="lcsh">
    <topic>Drugs</topic>
    <topic>Law and legislation</topic>
    <geographic>United States</geographic>
  </subject>
  <subject authority="lcsh">
    <topic>Drugs</topic>
    <topic>Law and legislation</topic>
    <geographic>European Union Countries</geographic>
  </subject>
  <classification authority="ddc">615.19 SHA-G</classification>
  <identifier type="isbn">0849319943 (alk. paper)</identifier>
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