Signant helped a leading sponsor meet accelerated timelines while generating high-quality COVID-19 vaccine safety and efficacy endpoint data.
Signant helped a leading sponsor meet accelerated timelines while generating high-quality COVID-19 vaccine safety and efficacy endpoint data.
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The informed consent process is fundamental to every clinical trial. Study participants must be provided with sufficient information to understand the study, its procedures and commitments, the possible treatments they may receive, and any possible...
For an effective eCOA platform that can meet any protocol requirements, study teams need more than just an app. Download this perspective paper to learn about the four pillars of eCOA success.
Signant’s eConsent solution helped a sponsor manage the consenting process complexities in their pediatric attention deficit hyperactivity disorder (ADHD) study located in Japan. This blinded case study explores how leveraging technology addresses the...
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