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Regulatory perspectives of Type II prodrug development and time-dependent toxicity management: Nonclinical Pharm/Tox analysis and the role of comparative toxicology

Wu, Kuei-Meng; Farrelly, James G.


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  <dc:creator>Wu, Kuei-Meng</dc:creator>
  <dc:creator>Farrelly, James G.</dc:creator>
  <dc:date>2007-07-01</dc:date>
  <dc:description>n/a</dc:description>
  <dc:identifier>https://zenodo.org/record/1259393</dc:identifier>
  <dc:identifier>10.1016/j.tox.2007.04.005</dc:identifier>
  <dc:identifier>oai:zenodo.org:1259393</dc:identifier>
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  <dc:title>Regulatory perspectives of Type II prodrug development and time-dependent toxicity management: Nonclinical Pharm/Tox analysis and the role of comparative toxicology</dc:title>
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