E-Technologies STREAM
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The Journey From File To Trial: Automating Regulatory To TMF
2/9/2021
In this webinar, we explore the value of automation between the Trial Master File (TMF) and Regulatory solutions. This connection can bridge the gap from the clinical trial to the regulatory filing, ensuring consistency of information while reducing duplicated data entry.
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The Medable Platform: Deep Evidence Generation
4/19/2024
Discover how Medable's platform technology enabled a top vaccine developer to accelerate study deployment and recruitment timelines.
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Electronic Data Capture Solutions For Your Phase I and Phase IV Studies
3/12/2025
Take a cost-effective approach to meet your study's data capture, management, and analysis needs with a solution customized to your clinical trial.
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Eliminating Custom Functions From EDC
8/13/2021
Watch this video to see how companies like ALCON are driving faster study builds and higher quality for complex studies with data-driven rules and dynamics.
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Seamless And Integrated Onboarding For Trial Participants
10/23/2024
Streamline your patient experience with a comprehensive, all-in-one solution that allows you to recruit, screen, and enroll participants remotely from the comfort of their own homes.
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Closing The "Compliance Gap" In TMF Archiving
8/15/2022
Discover how organizations are crossing this “compliance gap” with PhlexTMF for Viewing, an easily accessible TMF archive for internal use, audits, and inspections.
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The New Era Of Evidence Generation In Clinical Trials
6/19/2024
Learn how top pharmaceutical companies are using novel innovations to drive greater speed, scale, and access in clinical research than ever before in this webinar hosted by Musaddiq Khan, Vice President of DCT Solutions at Medable.
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Document Processing: A New Hope
8/8/2024
Tired of slow, error-prone document processing? Discover how top companies are boosting speed and accuracy while slashing costly rework. Watch now to learn how you can achieve TMF excellence faster.
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IQVIA eCOA: Amplifying The Patient's Voice
4/19/2024
Dive deep into the capabilities of IQVIA's eCOA with our expert Edward Bartels. He will focus on how to effortlessly create a diary, schedule site/participant assessments, and intuitively manage translations and compliance.
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Defining And Implementing The Right Oncology Digital Strategy
11/7/2024
A panel of oncology experts shares how top life science companies are using a combination of DHTs, ePROs, clinical trial platforms, and more to ease oncology research and drastically reduce timelines.