Products

Wemedoo’s oomnia system integrates powerful tools including CTMS, EDC, eTMF, ePRO, eCOA, eConsent, eSource, and RTSM, enabling end-to-end oversight and seamless collaboration across the clinical trial lifecycle.

Patient pre-screening AI assistant for clinical trial recruitment.

Health Studio is a clinical data platform built exclusively on Google Cloud. This low code platform allows organizations to build AI-enabled clinical solutions in a fraction of the time, unlocking all Google cloud resources and APIs with clicks not code. This allows organizations to introduce AI-enabled workflows and agent based applications with lower risk and cost and accelerate the time to realize the benefits. Further Health Studio's modular and customizable design integrates with existing t

Syncora is a cloud-based platform revolutionizing study startups for CROs, sponsors, and investigative sites. Born from relentless innovation, it automates workflows, captures and displays real-time data, and empowers teams to navigate complex startup processes with speed and precision. With a user-friendly interface, secure cloud backup, and a commitment to transparency, Syncora ensures timelines are met, delays are addressed proactively, and clinical trial operations run seamlessly from day on

Scienta Lab is an AI-powered platform pioneering Precision Immunology

Hipp Health offers an AI-native platform that streamlines and automates behavioral health practice management operations.

**HEKMA.ai** is an AI-powered clinical intelligence platform transforming how patients, healthcare providers, researchers, and life sciences organizations connect with clinical research. By combining intelligent patient matching, secure healthcare data integration, and advanced analytics, HEKMA.ai accelerates clinical trial recruitment, streamlines research workflows, and improves access to life-changing treatments. Committed to innovation, security, and inclusivity, HEKMA.ai is helping shape a

Catchtrial® eConsent enables participants to review and sign informed consent from anywhere using telemedicine-inspired technology. Compatible with Android and iOS, it removes the need for on-site visits and provides a seamless, mobile-first experience for patients.

Medigen® CTMS+ centralizes planning, monitoring, document management, product oversight and finances to streamline trials, reduce costs, and deliver faster, smarter results.

Diligent360 is an end-to-end Vendor management platform, built for the clinical trials industry. Diligent360 unifies the entire Vendor lifecycle from discovery and qualification through ongoing monitoring, so you can reduce delays, make risk-based decisions, and stay ahead of evolving compliance demands.

Clinion eConsent replaces manual consent processes with a digital system designed to improve patient onboarding and ensure compliance. Built within a unified platform, it enables real-time tracking, secure documentation, and seamless integration with Clinion EDC. What can you expect? ● Flexible Consent Models Support site-based, remote, and ePRO-linked consent workflows based on study needs. ● Faster Patient Enrollment Reduce onboarding timelines with digital consent and automated re-consenting

Delve Health combines eCOA/ePRO, wearable device integration, real-time analytics, and Concierge-as-a-Service™ into one clinical trial execution platform. Designed for sponsors, CROs, and research sites running hybrid and decentralized studies, Delve achieves 92–98% ePRO completion rates through proactive patient outreach in 120+ languages, device compliance monitoring, signal quality control, and site burden reduction. Used across oncology, CNS, cardiovascular, rare disease, respiratory, and po

Secure portal for central readers, KOLs, and investigators to review and share data and documents. • Built-in DICOM anonymization, centralized imaging assessment (MRI/CT), and remote monitoring. • Controlled reviewer access. • eCRF-like report forms. • Collaboration tools to support central review processes.