Jeeva is Calling for Early Adoption of their Remote Touchless Participant Recruitment and Electronic Informed Consent Platform
Are you planning to start participants' recruitment into an existing or new clinical research study...
When clinical investigators and study coordinators start planning a new study design in the new normal, speed and efficiency are paramount.
Running a clinical study takes careful planning. Whether this is your 1st clinical study or your 21st, the last thing you probably want to do is waste resources on delays caused by easily-preventable hurdles in data collection.
Traditionally, major bottlenecks occur during study startup, eligibility screening, informed consent (including assent in pediatric studies), and patient travel to the clinical site(s). Researchers eager to get the ball rolling on their study can save time and logistical burden by stopping these bottlenecks before they begin.
To read more, please download this free white paper.
Are you planning to start participants' recruitment into an existing or new clinical research study...
Our Jeeva Clinical cloud-based software provides a seamless solution that improves the experience of investigators...
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