How to Overcome Major Pitfalls When Planning Clinical Studies
When clinical investigators and study coordinators start planning a new study design in the new...
If you answered yes to any of these questions, read on…
Jeeva is soon launching its Cloud-based HIPAA compliant remote touchless electronic informed consent software (SaaS) to empower you to screen participants for eligibility and securely enrol them in your studies from the convenience of their own homes and mobile devices. Examples of research studies include patient registry, natural history, observational, or real-world evidence (RWE) studies by allowing you to configure a variety of studies and recruit participants remotely, electronically, securely, and safely.
Schedule your free consultation or a product demo now!
We are offering significant discounts to the first ten customers.
Jeeva™ is a Virginia-based company developing a secure SaaS platform to enable decentralized clinical research at scale. The software decreases study startup, recruitment timelines by 58% & reduces the logistical burdens on study teams & patients by 70% resulting in 30% cost savings.
Please contact Jeeva for more information.
When clinical investigators and study coordinators start planning a new study design in the new...
Our Jeeva Clinical cloud-based software provides a seamless solution that improves the experience of investigators...
In this interview from Rare Disease Day 2020 at the National Institutes of Health (NIH),...
Startup takes clinical trials to the homes of patients through utilisation of digital health technologies...