Ripple Science provides a HIPAA-compliant software suite that enables clinical trial sites, CROs, and sponsors to efficiently recruit, engage, and retain research participants throughout the trial process. By streamlining participant management and enhancing communication, Ripple improves enrollment rates and patient retention, leading to faster and more reliable study completions.
Funding
$10.8M raised to dateRaised to date based on public sources. This may differ from the amount the company actually raised and is based only on what is publicly available on the internet.
Founders
Product
Problem
Clinical trials often face challenges in recruiting, engaging, and retaining participants, leading to delays, increased costs, and potentially unreliable study results. Traditional methods of participant management can be inefficient, lack real-time visibility, and struggle to adapt to the complexities of decentralized or hybrid trial designs.
Solution
Ripple Science offers a HIPAA-compliant software platform designed to streamline participant management throughout the clinical trial lifecycle, from initial recruitment to final visit. The platform provides tools for building and maintaining local registries, tracking participant progress, automating communications, and managing team tasks. By centralizing study data and automating key workflows, Ripple Science enables clinical trial sites, CROs, and sponsors to improve enrollment rates, enhance patient retention, and accelerate study completion. The platform supports diverse study designs, including decentralized, virtual, and hybrid trials, while ensuring regulatory compliance with 21 CFR Part 11, HIPAA, GDPR, and SOC2 standards.
Target Audience
Ripple Science targets clinical trial sites, contract research organizations (CROs), pharmaceutical companies, medical device companies, and academic research institutions seeking to improve the efficiency and effectiveness of their clinical trials.
Features
- Direct-to-patient software platform designed for decentralized, virtual, and hybrid clinical trials
- Customizable workflows for recruitment, enrollment, engagement, and retention
- Automated email and task management to streamline team communication and follow-up
- Family ID tracking for studies involving multiple family members or siblings
- Real-time visibility into participant progress and study performance metrics
- Secure, computer-generated, time-stamped audit trails for all data modifications
- Integration with existing clinical trial management systems (CTMS) and electronic data capture (EDC) systems
- Local patient registry to build and maintain a pool of potential participants for future studies
- Compliance with 21 CFR Part 11, HIPAA, GDPR, and SOC2 standards