AI Enabled, Human Driven Software Solutions

Utilized by leaders in the pharmaceutical, biotech, and medical device industries and beyond, TrialAssure’s award-winning, AI-powered solutions are specifically designed to enhance data transparency and compliance while providing exceptional flexibility and support. Clients have praised TrialAssure for its ability to seamlessly integrate into their workflows, with one Associate Director noting, “The flexibility in workflow makes it a tool easily implemented in just about any organization.” Additionally, our commitment to collaboration is evident in feedback from a Senior Director at a leading clinical research organization (CRO), who emphasized that our AI knowledge and ability to co-create new solutions tailored to their needs is critical to their growth. With features that improve user experience and comprehensive training and support, TrialAssure empowers organizations to navigate the complexities of regulatory requirements confidently and efficiently.  

TrialAssure helps companies effectively handle Commercial Confidential Information (CCI) by leveraging its AI-powered platform, ANONYMIZE 3.0. Regulatory requirements, such as EMA Policy 0070 and Health Canada PRCI, mandate the protection of CCI in submissions, yet traditional manual processes remain labor-intensive and prone to errors, leading to significant costs. By utilizing specialized large language models, TrialAssure ANONYMIZE can accurately identify CCI topics by understanding the context and nuances of the data, which conventional keyword-based tools often miss. This results in an 80 percent reduction in processing time, a 90 percent decrease in human error, and substantial cost savings of 50 to 70 percent on labor. Additionally, the scalability of ANONYMIZE allows it to manage large document volumes effortlessly, enabling companies to redirect expert resources to more strategic tasks. By adopting AI-based anonymization, organizations can ensure compliance, enhance efficiency, and remain competitive in an evolving regulatory landscape. 

TrialAssure enables Sponsors to get a 360-degree view of their entire transparency landscape. Our clinical trial transparency software and tools provide your organization with the ability to visualize compliance status, manage workloads and resource allocations proactively, and leverage teams more effectively. With one data source for all of your clinical transparency and disclosure deliverables, you can be rest assured that duplication, errors, and data silos are never a bottleneck in your operational process. 

TrialAssure’s clinical trial transparency software suite has built-in alignment with all registry and regulatory requirements so that your outputs are acceptable to all external parties. Our team of industry experts keeps clients informed on impending regulation changes worldwide, allowing you to have confidence that your organization is in compliance now and in the future. 

Ensure COMPLIANCE WITH CONFIDENCE™ with TrialAssure REGISTRY. Submit information tailored to ClinicalTrials.gov, EudraCT, or any other global trial registry with the click of a button. Update information once in a single data record and your disclosures around the world will reflect that change! REGISTRY is entirely configurable and adaptable to internal business processes, including automation for more than 40 global registries. 

Our interactive workflows and data visualization tools help organizations meet and exceed transparency goals. Designed by industry experts, our powerful clinical trial transparency platform is uniquely equipped to significantly improve processes and team management. Manage handoffs between disclosure leads, study teams, and other responsible parties to ensure that all information is obtained in a timely manner. With TrialAssure as your technology solution, your organization will always be ahead of the curve. 

In today’s digital age, patients and caregivers expect easy access to information and transparency from clinical trials. TrialAssure allows you to develop, translate, and distribute easy-to-understand plain-language summaries and other critical documents in less than half the time. With TrialAssure, you’ll be able to meet global demand for non-technical clinical trial information dissemination, provide greater transparency, and promote patient engagement. 

Companies should avoid building generative AI tools from scratch and instead leverage TrialAssure’s expertise, knowledge, and tools to accelerate their AI adoption. Developing generative AI solutions independently comes with significant risks, including lengthy development cycles, compliance issues, and high failure rates, currently hovering around 90 percent for GenAI experiments. By utilizing LINK AI, organizations can access a scalable and highly configurable platform that supports specific use cases without the typical time and cost overruns associated with in-house development. LINK AI offers predictable costs, lower total cost of ownership, and faster time-to-value, allowing companies to achieve quick and measurable returns on their investment. With proven success in processing vast amounts of clinical data and drafting scientific documents rapidly, LINK AI empowers businesses to implement high-value generative AI use cases effectively and efficiently, ensuring compliance with global medical and regulatory standards from the outset.