eConsent - The Good, the Bad, and the Regulatory

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Speaker: Gabe Westerlund

For clinical trial patients, the informed consent process has long been in need of optimization. High patient attrition rates indicate that we’re not doing enough to ensure patients truly understand the risks and burdens inherent in clinical trial participation. We can do better. As we rethink informed consent to improve it for all stakeholders - especially patients - electronic informed consent (eConsent) has a key role to play. Join Gabe Westerlund, Solutions Engineer at Medrio, as he explores the opportunities presented by the advent of eConsent, and how the consent process is evolving to deal with changes in technology, a focus on patient centricity, shifting guidance, and regulatory pressures

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