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At Trial Genasys, we're not just building AI—we're asking better questions. What if clinical trials could run 40% faster? What if regulatory compliance was no longer a bottleneck? What if trial outcomes could be predicted before the first patient is enrolled?
Our mission is rooted in a powerful belief: technology should serve humanity by accelerating access to life-changing treatments. That’s why Trial Genasys was created—to eliminate the inefficiencies and uncertainties in traditional clinical research, and to enable a smarter, more adaptive clinical ecosystem.
We exist because patients deserve better, because time matters, and because the future of healthcare depends on platforms that are built to evolve. Trial Genasys is engineered to meet this need, offering sponsors a truly intelligent approach to clinical research. Our platform delivers real-time trial intelligence powered by advanced analytics, enabling faster decision-making and better visibility across every stage of the trial. Through automated document creation aligned with ICH, FDA, and EMA standards, Trial Genasys streamlines regulatory submissions without compromising quality or compliance.
Designed for Disruption. Built for Compliance. Trusted for Innovation.
Every line of code in Trial Genasys is written with one purpose: to solve the real-world problems facing clinical operations today. Built by a cross-functional team of scientists, engineers, medical writers, and regulatory experts, our platform is shaped by deep domain understanding and future-facing vision.
Whether you're preparing an IND or scaling a Phase III trial, Trial Genasys empowers your team at every stage with intelligent, AI-driven capabilities. By leveraging machine learning-powered insights, the platform helps you make smarter, faster decisions grounded in real-time data. Our AI-assisted authoring tools generate audit-ready documentation on demand, ensuring regulatory compliance with minimal manual effort. Trial Genasys also enables seamless integration with existing EDC, CTMS, and eTMF systems, simplifying data management and accelerating timelines. Designed for global collaboration, the platform connects teams across languages, geographies, and regulatory frameworks—removing barriers and driving operational alignment.
At Trial Genasys, we redefine the creation of clinical User Manuals and Guides through intelligent, AI-powered content development. Our platform enables seamless implementation and deep comprehension of clinical systems, protocols, and digital tools—empowering research teams, investigators, and site staff with personalized, easy-to-follow instructions tailored to study-specific platforms and procedures.
Every manual generated by Trial Genasys is backed by adaptive AI methodologies that ensure clarity, accuracy, and regulatory compliance. Whether it’s for data capture systems, reporting tools, or patient-facing technologies, our dynamic documentation evolves with your study needs—ensuring users are equipped with the critical knowledge to stay aligned with SOPs, reduce errors, and streamline operations across trial sites.
Trial Genasys goes beyond static documentation by delivering intelligent, up-to-date, and audit-ready user materials. This helps reduce onboarding time, enhance operational efficiency, and ensure your teams are ready to perform—right from day one.
Reach out to our dedicated team for any inquiries, appointment scheduling, or support.
