Patient Data Reporting Videos
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What Does A Pragmatic Approach To PMC/PMRs Look Like For Sponsors?
7/23/2024
Learn how integrating technology into existing workflows can help sites and sponsors reduce the burden associated with data collection in the post-marketing setting.
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Automated Data Transfer For Cancer Clinical Trials Offers Time And Resource Savings
7/23/2024
Uncover how Flatiron Clinical Pipe™ significantly reduced inefficiencies and errors in cancer clinical trials by automating data transfer, cutting CRF submission time to just 43 seconds.
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Watch EHR-To-EDC Connector, Flatiron Clinical Pipe™ In Action
7/23/2024
Discover how Flatiron Clinical Pipe™, the top EHR-to-EDC connector, saves time, reduces data monitoring costs, accelerates data cleaning, and helps you reach study milestones faster.
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How EHR-To-EDC Tech Can Streamline Study Data Acquisition, Management
7/23/2024
Recent assessments reveal that data verification, management, and monitoring account for over 25% of clinical research costs. See how Flatiron's Clinical Pipe, saves time and reduces costs.
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Signant StudyIQ Trial Management Suite Overview
7/16/2024
See how our dynamic and rich reporting solutions facilitate high-quality clinical data and support efficient trial management. All reports, dashboards, and analytics come standard with our eCOA solutions.
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Customer Testimonial – Keya Watkins, SVP, Oncology, Catalyst
6/26/2024
Join Keya Watkins, SVP of Oncology at Catalyst, as she discusses the transformative impact of Rave EDC in enhancing competitiveness and sponsor engagement in oncology trials.
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Customer Testimonial – Chuck Bradley, Clinical Development & Operations Consultant
6/26/2024
In this testimonial, a Clinical Development & Operations Consultant highlights the industry-standard Medidata platform and the significant benefits of using a consistent system across sites.
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Customer Testimonial – From CRA To Management
6/26/2024
Join Brittany Erlandson, Sr. Manager of Clinical Operations at QuidelOrtho, as she shares her journey from CRA to management and the crucial role of Medidata's EDC system in enhancing efficiency.
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Veeva eCOA Demo
6/24/2024
See firsthand how this modern build platform, which includes a ‘one-click’ library of pre-validated questionnaires, reduces build times by 75% and means mid-study updates can be actioned in minutes.
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Vault Safety-EDC Connection
6/24/2024
Learn how to automate the flow of Serious Adverse Event (SAE) information between data management and safety systems, enabling more timely responses by Pharmacovigilance (PV) teams.