Articles, App Notes, Case Studies, & White Papers
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Gradually Investing In Direct Data Capture Is Inevitable
2/2/2023
Given study decentralization and the many electronic sources of data now available, it is time for sponsors and contract research organizations to face the inevitable: EDCs need to be “sunsetted.”
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How Small And Mid-Sized Biopharmaceutical Companies Can Easily Achieve Digital Innovation For Their Clinical Data
7/12/2022
Discover how forward- thinking life science companies are defining their vision and looking for like-minded partners to execute information technology.
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Everest Group Life Sciences EDC Products PEAK Matrix® Assessment 2024
2/11/2025
This Everest Group report examines Medidata’s Rave EDC and its impact on the clinical development value chain of life sciences.
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Navigating Audit Trail Data Regulations And Accessibility Changes
5/15/2024
Data is the single most important thing in a clinical trial. Leverage the power of clinical trial data with effective utilization and access in a changing regulatory landscape.
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RWD: More Than Just Another Acronym
10/19/2023
Uncover how real-world data can not only be used for any type of clinical trial, but study sponsors can also use RWD to inform all stages of a study.
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Expand Clinical Trial Recruitment With Advanced Analytics And AI
9/17/2025
Using advanced analytics and AI can help clinical trial leaders identify and enroll a broader, more diverse patient population, accelerating research.
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eCOA Evolution: Have We Overcomplicated It?
11/21/2024
eCOA has evolved from simple data collection to complex patient engagement platforms, raising concerns about added complexity. Explore innovative tools aimed at simplifying this complexity.
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Harnessing The Power of Real-World Data In Clinical Trial Planning
2/20/2024
As the availability of RWD grows, it creates opportunities for sponsors to use true patient insights to support their clinical strategy and bring treatments to patients in need.
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Perspective On The FDA's Final Digital Health Technologies Guidance
1/24/2024
Review the final release of "Digital Health Technologies for Remote Data Acquisition in Clinical Investigations”, where the FDA acknowledges DHT value and the increasing use of them in clinical trials.
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Advancing The Implementation Of ICH E17
5/13/2025
Explore the ICH E17 guidelines that provide a harmonized framework for designing and conducting multiregional clinical trials (MRCTs) to meet the regulatory expectations of multiple regions.