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Revolutionizing Clinical Trials with Flatiron Clinical Pipe™

Introduction to Flatiron Clinical Pipe™

Flatiron Clinical Pipe™ is an innovative EHR-to-EDC application that revolutionizes the way clinical trial data is managed. With the ability to capture and transfer both structured and unstructured data with ease, this solution streamlines the entire data collection process. By offering higher data quality and more efficient data management, Flatiron Clinical Pipe™ transforms the clinical trial experience for sponsors, CROs, and clinical trial sites.

Key Advantages of Flatiron Clinical Pipe™

Flatiron Clinical Pipe™ stands out in the industry with its key advantages. With over 5 years of proven technology, this solution has been used by 35+ sponsors, including the top 10 pharma companies globally. The platform is connected with 85 sites and has seen a 4X growth since 2022. Offering flexibility across 15+ unique indications, Flatiron Clinical Pipe™ ensures that it can cater to diverse study needs.

Differentiated Data Management Approach

Flatiron Clinical Pipe™ pioneers access to both structured and unstructured data. Structured data includes existing discrete data fields in the EHR, while unstructured data is processed by Flatiron's leading abstraction team. The platform has abstracted over 800 million data points to date, catering to a wide range of data requirements in clinical trials.

Key Features and Functionality

With Flatiron Clinical Pipe™, data transfer from EHR to EDC is rapid and seamless, reducing manual data entry errors and accelerating data cleaning timelines. The platform achieves eSource goals by mirroring EMR/EHR data and eliminating the need for source data verification. It integrates seamlessly with popular systems like OncoEMR®, Epic®, Cerner®, and Medidata Rave®, while ensuring strict security and compliance measures are met.

Support and Testimonials

Flatiron Clinical Pipe™ offers high-touch support services, including training, onsite and virtual support, and expert assistance to ensure smooth onboarding and ongoing success for sites and sponsors. Testimonials like that of Dannelle M. Palmer, COO of OncoBay Clinical, highlight the transformative impact of Flatiron Clinical Pipe™ on the clinical trial process.

Transforming Clinical Trial Experiences

In conclusion, Flatiron Clinical Pipe™ redefines the way clinical trials are conducted. By offering a comprehensive solution for data management, security, and support, this platform empowers trial teams to achieve higher data quality, increased efficiency, and faster study milestones. Contact Flatiron today to learn how Clinical Pipe™ can transform your next clinical trial experience.


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Revolutionizing Oncology Clinical Decision Support with Flatiron Assist™

Empowering Clinicians with Innovative Treatment Insights

Flatiron Assist™ is an EHR-integrated, oncology-specific clinical decision support platform that revolutionizes the way clinicians access and implement evidence-based medicine, clinical research, and site-specific preferences at the point of care. This powerful tool prioritizes the latest treatment guidelines and insights, ensuring that healthcare providers are equipped with the most up-to-date information to optimize patient care.

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Empowering Oncology Research with Real-World Data Solutions from Horizon Datascapes

Tailored Real-World Data Solutions for Oncology Portfolio

Horizon Datascapes, provided by Flatiron Health, offer tailored real-world data solutions to meet the unique needs of oncology portfolios. With over 4 million patient records and 1.5 billion data points, these datasets are designed to address specific use cases efficiently and effectively.

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Revolutionizing Cancer Care: The Impact of Flatiron Health in Oncology Research and Treatment

Who We Are

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Revolutionizing Oncology Clinical Trial Recruitment with OncoTrials®

Efficiently match and screen eligible patients

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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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