Latest Stories

Video eConsent How we Bring the Site to the Patient

Assuring patients are well informed and protected is always vital to the clinical trial process. Yet, it’s estimated that over one-third of eligible patients enrolled in trials will fail to submit their consent due to a lack of understanding of the informed consent document and procedure. ClinOne continues to address this with our eConsent module, […]

ClinOne brings remote monitoring to trials with BioIntelliSense FDA-cleared BioSticker™

ClinOne announces today its strategic collaboration with BioIntelliSense to combine continuous health monitoring and clinical intelligence with the ClinOne ClinTrialConnect™ patient portal platform.  The addition of the FDA-cleared BioSticker™ single-use device provides an effortless trial participant experience enabling 30-days of continuous vital sign monitoring.  “With BioIntelliSense, we will be able to capture a wide array of medical-grade […]

ClinOne’s eConsent for Sites: For Better Compliance and Significant Savings

Our eConsent provides technology critical to clinical trial stakeholders that will eliminate any violations related to Information Assurance and Privacy (ICF) compliance while eliminating hundreds of work hours for sites, as well. Improved workflow for patient consent:  The technology uses our e-signature partner’s electronic signature platform, where the PI and patient can both sign remotely from […]

Dosing Manager by ClinOne Accomplishes 97% Patient Self-Dosing Compliance for Sponsors

ClinOne’s published compliance rate with patient self-dosing compliance is 97% at 10 months with the Dosing Manager module, a major asset to clinical trial sponsors.Since clinical trials rely on precision in self-dosing to keep trials on track and patients compliant, ClinOne’s Dosing Manager solves for this and does so extremely effectively. The typical pain points and […]

ClinOne releases revised reporting for study performance and complete trial insights

Today, ClinOne launches its redesigned reporting solution which brings complete transparency around site and patient compliance to sponsors. This new additional reporting functionality provides sponsors with information and analysis of all their ongoing studies on ClinOne. Trial sponsors may run customized reports to analyze their usage across the core platform or for a specific module.This […]

Video eConsent by ClinOne: Bringing the Site to the Patient

Assuring patients are always well informed and protected is vital to the clinical trial process. Yet, it’s estimated that over one-third of eligible patients enrolled in trials will fail to submit their consent due to a lack of understanding of the informed consent document and procedure. ClinOne addresses this with our eConsent module, now with […]