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Revolutionizing Oncology Clinical Trial Recruitment with OncoTrials®

Efficiently match and screen eligible patients

Oncology clinical trial programs are often intricate and multifaceted, presenting a challenge in finding suitable patients for participation. However, with OncoTrials®, this process is simplified and streamlined. Clinical research teams can now swiftly and efficiently assess and confirm eligible trial patients, enhancing the overall recruitment process. By utilizing Electronic Health Record (EHR) data, OncoTrials® enables teams to view filtered and prioritized patients that are at crucial treatment decision points. This not only builds confidence in patient eligibility but also ensures that no potential participant is overlooked. Additionally, the system offers research badges that identify potential patients at the point of care, facilitating proactive patient recruitment.

No patient left behind - Find the right patients

With OncoTrials®, the focus is on ensuring that no patient is left behind when it comes to clinical trial recruitment. By surfacing eligible patients at the right time, this solution reduces the screening volume and optimizes the patient identification process. By leveraging operational reports, research teams can gain insights into program performance and make informed decisions based on data-driven analytics. Furthermore, the system allows for easy tracking of patients by providing status updates on candidates, consented individuals, and ineligible patients, ensuring that each patient's journey through the clinical trial process is efficiently monitored and managed.

Case Study: Prospective Clinico-Genomic Study

A notable example of the impact of OncoTrials® is showcased in the Prospective Clinico-Genomic Study conducted by Flatiron Health®, Foundation Medicine, and Genentech. This study highlights the successful collaboration and innovative platform developed to execute real-world studies in oncology research. By leveraging the capabilities of OncoTrials®, the teams were able to efficiently identify potentially eligible patients and manage them seamlessly within the study watchlist. The feedback from Jamie M. Hodgson, a Clinical Research Manager, underscores the efficiency and effectiveness of the system in streamlining patient identification and recruitment processes.

Clinical Research Product Suite

Flatiron Health® offers a comprehensive clinical research product suite that aims to reduce operational burdens, enhance operational efficiencies, lower costs, accelerate drug delivery to diverse patient populations, and provide robust support throughout the trial process, from design to FDA submission. The suite includes Protocol Optimization and Patient Identification by Flatiron, Flatiron Clinical Pipe™, and Prospective Evidence Generation. By incorporating technology-supported solutions, Flatiron Health® is reimagining the infrastructure of cancer care, revolutionizing the landscape of clinical research, and driving advancements in oncology research.


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Empowering Clinical Trial Diversity: Flatiron Health's Comprehensive Solution

Understanding the Challenge

Clinical trials have long struggled with underrepresentation from various demographic groups, hindering the ability to understand treatment efficacy across different populations. This lack of diversity exacerbates health disparities and limits outcomes for marginalized communities. The FDA's recent guidance mandates sponsors to create diverse action plans to ensure representative testing. Failure to comply could lead to delays and increased costs.

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Revolutionizing Oncology Evidence Generation with Flatiron Horizon

Flexible Real-World Evidence Solutions

Flatiron Health's Evidence Solutions offer a flexible approach to generating both prospective and retrospective real-world evidence. Whether you are conducting ambitious research or facing critical decision points, Flatiron provides the necessary data and support in a manner that helps you achieve your goals efficiently. By leveraging their solutions, researchers can progress faster and gain valuable clinical, analytical, and regulatory assistance.

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Empowering Oncology Real-World Evidence: Flatiron Health Solutions

Tailored Solutions for Oncology Evidence

Flatiron Health stands out with its in-house expertise, offering tailored oncology evidence solutions across the biopharma lifecycle. The experts at Flatiron address a wide range of research areas including natural history studies, comparative effectiveness research, protocol optimization, patient recruitment strategies, uptake monitoring, transportability assessments, dosing patterns, drug safety, and strategic regulatory interactions and briefing book development. Their focus on unique nuances of research questions and deep understanding sets them apart in the industry.

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Securing Patient Data with Flatiron Health's Confidentiality Commitments

Understanding Confidential Information with Flatiron Health

Flatiron Health acknowledges the critical role of patient data in improving cancer care and research. As a subsidiary of Roche Holding Ltd., the company prioritizes safeguarding confidential information received from customers, partners, and patients. The definition of confidential information includes personal, sensitive, or proprietary data that is not publicly available and is shared in the context of business interactions. Flatiron ensures compliance with privacy laws and internal policies while handling identifiable patient-level information.

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Revolutionizing Clinical Trials with Flatiron Clinical Pipe™

Enhancing Data Quality and Efficiency

Flatiron Clinical Pipe™ offers a pioneering EHR-to-EDC application that significantly improves data quality and efficiency in clinical research. By capturing and transferring both structured and unstructured data seamlessly, this innovative solution streamlines the data management process. With just a few clicks, researchers can accelerate data cleaning timelines, reduce queries, and achieve study milestones faster, creating a new trial experience that enhances overall research outcomes.

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