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  <titleInfo>
    <title>Approved</title>
    <subTitle>The Life Cycle of Drug Development</subTitle>
  </titleInfo>
  <name type="personal">
    <namePart>Chirmule, Narendra-Editor</namePart>
    <role>
      <roleTerm authority="marcrelator" type="text">creator</roleTerm>
    </role>
  </name>
  <name type="personal">
    <namePart>Ghalsasi, Vihang</namePart>
  </name>
  <typeOfResource>text</typeOfResource>
  <originInfo>
    <place>
      <placeTerm type="text">Switzerland</placeTerm>
    </place>
    <publisher>Springer</publisher>
    <dateIssued>2025</dateIssued>
    <issuance>monographic</issuance>
  </originInfo>
  <language>
    <languageTerm authority="iso639-2b" type="code">ENG</languageTerm>
  </language>
  <physicalDescription>
    <extent>xxv, 634 Hard Bound</extent>
  </physicalDescription>
  <abstract>This book offers a detailed and insightful look into the modern drug development process, highlighting how innovation, quality, and regulatory compliance come together to create safe and effective medicines. It explores the rise of biotherapeutics and explains key stages such as pharmacology, clinical trials, manufacturing, and quality assurance. With references to regulatory frameworks like the Food and Drug Administration (FDA), it serves as a valuable guide for understanding the complexities of bringing new drugs to market. Ideal for students, researchers, and professionals in the pharmaceutical and healthcare fields.</abstract>
  <tableOfContents>Drug development
Biotherapeutics
Pharmaceutical industry
Pharmacology</tableOfContents>
  <subject>
    <topic>C-10:Popular Science</topic>
  </subject>
  <classification authority="ddc">/CHI</classification>
  <identifier type="isbn">9783031817861</identifier>
  <recordInfo>
    <recordChangeDate encoding="iso8601">20260502164631.0</recordChangeDate>
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