News & Analysis on Clinical Trial Services & Contract Research And Development
Are you curious why more Sponsors choose digital data collection methods over the traditional pen and paper? Read this recent white paper to discover the common risks associated with paper. You’ll also learn why industry experts predict that electronic patient-reported outcomes (PROs) are the future of clinical research.
Paid for and content provided by Signant Health
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...
For more product information visit Signant Health.