News & Analysis on Clinical Trial Services & Contract Research And Development
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 advanced document management required to accommodate multiple consent forms and implement user-specific language requirements.
Readers will learn the benefits of eConsent solutions in Japan-based studies as well as the results of the ADHD study.
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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.
Today, sponsors and study teams often struggle to support the growing variety and volume of clinical data. The right technology thought will help your study teams conduct comprehensive reviews of all the standardized data at once.
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