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  <titleInfo>
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    <title>tment optimisation in drug development</title>
    <subTitle>: study : Panel for the Future of Science and Technology</subTitle>
  </titleInfo>
  <name type="corporate">
    <namePart>Parlamento Europeo</namePart>
    <namePart>Dirección General de Servicios de Estudios Parlamentarios</namePart>
  </name>
  <typeOfResource>text</typeOfResource>
  <genre authority="marc">technical report</genre>
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    <place>
      <placeTerm type="text">Brussels</placeTerm>
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    <publisher>European Union</publisher>
    <dateIssued>March 2020</dateIssued>
    <dateIssued encoding="marc">2020</dateIssued>
    <issuance>monographic</issuance>
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  <language>
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    <extent>V, 70 p. ; 1 documento PDF</extent>
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  <abstract>The development of novel health technologies is a complex and costly process that follows an extensive set of regulatory guidelines and legal provisions intended to ensure that the treatments reach the patients that need them in a highly controlled and standardised manner</abstract>
  <targetAudience authority="marctarget">specialized</targetAudience>
  <note type="statement of responsibility">/ EPRS - European Parliamentary Research Service</note>
  <note>Bibliografía: p. 66-70</note>
  <note>Reproduction and translation for non-commercial purposes are authorised, provided the source is acknowledged and the European Parliament is given prior notice and sent a copy.</note>
  <subject authority="">
    <topic>Sanidad digital</topic>
  </subject>
  <subject>
    <topic>treatment optimisation</topic>
  </subject>
  <subject>
    <topic>clinical drug</topic>
  </subject>
  <subject>
    <topic>treatment</topic>
  </subject>
  <subject>
    <topic>patient</topic>
  </subject>
  <subject>
    <topic>public health</topic>
  </subject>
  <subject>
    <topic>industry</topic>
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  <identifier type="isbn">978-92-846-6037-7  </identifier>
  <identifier type="uri">https://www.europarl.europa.eu/RegData/etudes/STUD/2020/641511/EPRS_STU(2020)641511_EN.pdf</identifier>
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