State of Digital Clinical Trials is a Veeva podcast hosted by Manny Vazquez, Director, Clinical Data Strategy. Manny will be speaking to a series of expert guests from across pharma, biotech, and CROs to discuss their experiences, challenges, and ideas for the future of digital clinical trials. Will new technology make clinical trials more patient- and site-centric?
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State of Digital Clinical Trials is a Veeva podcast hosted by Manny Vazquez, Director, Clinical Data Strategy. Manny will be speaking to a series of expert guests from across pharma, biotech, and CROs to discuss their experiences, challenges, and ideas for the future of digital clinical trials. Will new technology make clinical trials more patient- and site-centric?
<p>This week, Richard Young speaks to Ken Getz, executive director and research professor at Tufts Center for the Study of Drug Development. </p>
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<p>Already well-known in our industry for his pioneering research on protocol design complexity and trial efficiency, Ken’s most recent study found that the <a href="https://www.appliedclinicaltrialsonline.com/view/shining-a-light-on-the-inefficiencies-in-amendment-implementation">average number of amendments per protocol increased by almost 60% over the past seven years</a>. </p>
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<p>In this episode, Richard and Ken debate whether clinical research is striking the right balance in its approach to risk and innovation, the problem-solving role played by sites, and <a href="https://www.ciscrp.org/">CISCRP</a>’s work to improve public trust in scientific advances.</p>
<p><br>Subscribe to <em>State of Digital Clinical Trials</em>, a Veeva podcast, to get new episodes as soon as they are released.</p>
Unblinded: A Clinical Trial Podcast
State of Digital Clinical Trials is a Veeva podcast hosted by Manny Vazquez, Director, Clinical Data Strategy. Manny will be speaking to a series of expert guests from across pharma, biotech, and CROs to discuss their experiences, challenges, and ideas for the future of digital clinical trials. Will new technology make clinical trials more patient- and site-centric?