FDA MyStudies, open-source platform to help organizations collect and report real world data for regulatory submissions, now available on Google cloud.
Want to dig deeper into real world evidence?
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Industry Assessment of the Contribution of Patient Support Programs, Market Research Programs, and Social Media to Patient Safety
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Jeremy Jokinen et al.
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Advancing the Use of Real World Evidence for Regulatory Decision Making
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Barbara Lopez Kunz, Nicole Mahoney
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Potential Use of Artificial Intelligence for Regulatory Intelligence
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Mark Mayer et al.
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Editorial: Electric Guitars, Photoshop, and Clinical Trials
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Alberto Grignolo
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When Is Real World Evidence Ready for Prime Time?
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Nancy Dreyer
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Advancing the Canadian Dialogue on RWE in Regulatory Decisions
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Judith Glennie
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FDA's Real World Evidence Program Moving Forward
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Jacqueline Corrigan-Curay, David Martin
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Editorial: Building Trust in RWE Will Support Clearer Regulatory Uses
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Gregory Daniel
Therapeutic Innovation & Regulatory Science
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Nurturing Growth of RWD into RWE in Japan
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Manami Yoshida, Shinzo Hiroi
Global Forum
Want to learn more?
Learn more about collecting and reporting real world data at our Digital Technology in Clinical Trials conference in Boston and Real World Evidence Conference in San Diego.
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