Attracting a participants from diverse demographics can be tough, but Jeeva's platform expands your reach through virtual engagement tools, helping you recruit a broader, more representative sample seamlessly.
Consistently tracking changes in skin conditions is crucial and may often require photo capture of the affected area. Our real-time data capture allows for precise and continuous monitoring of skin health, ensuring accurate remote assessments.
Participants often miss application schedules or diary entries. Jeeva simplifies adherence with automated scheduling, reminders, and participant engagement portal, ensuring everyone stays on schedule with minimal effort.
Our unified platform eliminates the need for downstream integration for most part. Avoid Juggling between fragmented tools. Jeeva offers a centralized platform to streamline data management with process automation.
Protecting sensitive participant data is paramount. Jeeva’s robust security features ensure that all collected data is stored securely, giving both researchers and participants peace of mind.
Navigating the complex web of regulatory requirements is a common hurdle. With Jeeva, you’ll have comprehensive documentation and compliance checks built-in, making regulatory adherence straightforward and stress-free.
With Jeeva, you have the convenience of accessing all your cosmetics and skincare clinical studies through a single login, providing a unified platform to manage multiple trials effortlessly, keeping everything organized and at your fingertips.
Jeeva’s software automates repetitive tasks such as data entry and participant follow-ups, freeing you from manual work so you can focus on the insights that matter most in your skincare and cosmetics research.
Communication is key, but it shouldn’t be a burden. Jeeva streamlines interactions with participants and between team members through automated updates and centralized messaging, making sure everyone stays informed with minimal effort.
By simplifying study setup and participant engagement, Jeeva accelerates the process to your first patient first visit, cutting down lead times so you can start collecting valuable data sooner rather than later.
You may derive most value when your clinical operations infrastructure is not set up yet. However, even if some of your infrastructure is in place, Jeeva can complement what you have with modularity and automation.
There’s no upfront CapEx. Our pricing is usage-based, and partners see ROI by reducing site coordination and compliance overhead.
That’s exactly why sponsors and CROs with team sizes under 50 people love Jeeva. You get big CRO capabilities without the cost or complexity.
Jeeva is fully validated, GCP-aligned, 21 CFR Part 11 and GDPR compliant. We’re already used by academic medical centers and sponsors in regulated trials.
Jeeva streamlines protocol adherence by automating reminders for participants, ensuring that skincare routines and application schedules are followed. This keeps data consistent and reduces drop-off rates significantly.
Data security is a top priority for Jeeva. The platform employs robust security protocols and encryption measures, safeguarding sensitive participant information and providing a secure environment for data storage and sharing.
Definitely! With Jeeva, you can manage all of your clinical studies from a single login interface, which simplifies oversight and coordination across multiple trials, streamlining your entire research process.
Jeeva’s comprehensive documentation features and built-in compliance checks make it easier to meet regulatory requirements. This ensures your trials adhere to industry guidelines, saving time and enhancing your study’s credibility.
Enterprise Jeeva eClinical Suite enables the sponsor team to semi-automate clinical research workflows, including study configuration, patient screening and recruitment, clinical data management, and digital patient engagement.
Still Curious If Jeeva Human-Centric Clinical Research Software Is a Good Fit for Your Study?
