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          <dc:identifier>https://hdl.handle.net/10776/13232</dc:identifier>
                  <dc:date>2021-03-01</dc:date>
                  <dc:language>eng</dc:language>
                  <dc:contributor>Meek, Caroline</dc:contributor>
          <dc:contributor>Tuoti, Whitney Alexandra</dc:contributor>
          <dc:contributor>Arizona State University. School of Life Sciences. Center for Biology and Society. Embryo Project Encyclopedia.</dc:contributor>
          <dc:contributor>Arizona Board of Regents</dc:contributor>
                  <dc:rights>open access</dc:rights>
          <dc:rights>http://creativecommons.org/licenses/by-nc-sa/3.0/</dc:rights>
                  <dc:description>The problem of whether women should be involved in drug research is a question of who can assume risk and who is responsible for disseminating what specific kinds of information. The problem tends to be framed as one that juxtaposes the health of women and fetuses and sets their health as in opposition. That opposition, coupled with the inherent uncertainty in testing drugs, provides for a complex set of issues surrounding consent and access to information.</dc:description>
                  <dc:subject>Research--Moral and ethical aspects</dc:subject>
          <dc:subject>Research</dc:subject>
          <dc:subject>Moral and ethical aspects</dc:subject>
          <dc:subject>Ethics, Research</dc:subject>
          <dc:subject>Research Ethics</dc:subject>
          <dc:subject>Ethics</dc:subject>
                  <dc:title>Thesis: A History and Analysis of Drug Labeling Policy for Pregnant and Lactating Women and Women&#039;s Involvement in Clinical Drug Research from 1970 to 2014</dc:title></oai_dc:dc></metadata></record></GetRecord></OAI-PMH>
