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xtalks.com, webinar
Thursday, February 24, 2022 | 1pm EST
Who Should Attend?This webinar will appeal to: - C-Suite:
- CEO
- CMO (Chief Medical Officer)
- COO (Chief Operating Officer)
- CIO (Chief Information Officer)
- Executive Leadership:
- S/VP of R&D
- S/VP of Clinical Development
- Therapeutic Area heads (e.g., oncology, neuro)
- VP of Clinical Operations
- VP of Clinical Data Management
- Study Management:
- Directors/Managers of Clinical Operations
What You Will LearnWebinar attendees will: - Review how trial sponsors are obtaining a far clearer understanding of how a drug is performing against safety and efficacy endpoints while the study is underway, without increasing alpha-spend
- Examine how unified insight into live data helped one biopharmaceutical company achieve the industry’s first-ever successful New Drug Application (NDA) in a highly challenging indication — one where dozens of other sponsors had tried and failed
- Break down the myth that it is too difficult and costly to achieve a single, unified view across a study or program from all clinical and operational data sources
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Organized by:
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xtalks.com |
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Invited Speakers:
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SpeakerPatrick Keenan, Chief Strategist, Prevail InfoWorksAs Chief Strategist for Prevail InfoWorks, Patrick Keenan draws on more than 15 years of experience in life sciences technology and operations to ensure Prevail’s innovative technology helps trial sponsors and CROs successfully meet today’s pressing clinical development and regulatory challenges. In addition to leading the company’s business and market strategy, he collaborates closely with Prevail’s existing and prospective customers to thoroughly understand their key business requirements and develop the most effective solutions.
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Deadline for Abstracts:
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Registration:
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https://xtalks.com/webinars/analyze-data-quality-in-live-studies-without-unblinding-or-spending-alpha/
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E-mail:
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shunte@xtalks.com
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