What the Future Holds for Informed Consent

June 30, 2016
Mika Lindroos, Director of Product Management at CRF Health, discusses the advantages of electronic informed consent in clinical trials and how by integrating this process with eCOA technologies, researchers can reduce burden for study teams, decrease regulatory risk, increase participant comprehension, and improve overall study outcomes. Courtesy of PharmaFocus (original link: http://edition.pagesuite-professional.co.uk/launch.aspx?eid=b3114258-2357-4dee-b791-295cd1220624&pnum=18)
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The Value of Electronic Informed Consent
The Value of Electronic Informed Consent

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Innovations in e-Consent: Reducing Regulatory Risk While Improving Participant Comprehension
Innovations in e-Consent: Reducing Regulatory Risk While Improving Participant Comprehension

<p>Informed consent has a major impact on regulatory compliance, enrollment rates and expenses across the l...

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