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From Study Design to Submission: The Role of AI Throughout the Clinical Research Journey
Artificial intelligence (AI) is transforming the clinical research landscape. It is being used to optimize how data is collected, organized and moved through electronic data capture (EDC) platforms. Researchers are increasingly curious about its potential to streamline the entire clinical trial process. From study design to data submission, AI is helping clinical trials become more…
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Accelerate Your Study Starts – How to Avoid Database Go-Live Delays with TrialKit’s EDC System
Delays in study start-up and database go-live can create significant challenges in clinical trials. First off, delays cost money – as much as $500,000 per day according to a recent study from the Tufts Center for the Study of Drug Development (Tufts CSDD). Utilizing the right tools within an electronic data capture system like TrialKit…
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Avoiding Clinical Data Vaporware – Even More Questions to Ask eClinical Software Providers
In our last blog, we brought up the topic of vaporware in clinical research data management. Clinical trials require a lot of tech to collect, manage, and analyze data, and there are so many providers putting out claims about what their products can do. Certainly, we’ve all been in positions where a potential vendor seems…
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Improve Data Collection with These Tips for Electronic Case Report Form (eCRF) Design
In this post, we reveal some tips and techniques for designing powerful and purposeful CRFs that fuel accurate data collection.
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What You Need to Know About Validation in Clinical Data Management
Leveraging technology tools can make your research study validation significantly more efficient and accurate. Read on to find out which software features can help you validate with ease.
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How to Shorten the Duration of a Clinical Study Build
Shaving time off the trial design and study build process enables research teams to dedicate more resources to other important tasks. Discover some of the ways to accomplish a shorter study build in this post.
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Case Report Forms in Clinical Trials: Did you Ask the Right Questions?
When creating CRFs in a clinical study build, it’s important to ask the right questions, but it is equally important to ask in the right way. Let’s take a closer look at different form fields and how to leverage them to prompt more accurate responses in the data collection process.
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Why More Sponsors Are Taking Control of Clinical Trial Study Builds
Sponsor companies needn’t feel restricted to sourcing out their study builds to CROs. Many times, they can accomplish their own builds with the right EDC system – and save considerable resources.
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CRF Validation Best Practices: Building Reliable Clinical Trial Databases
Validation of case report forms is a necessary, but often painful, process. The IQ/OQ/PQ standard, which we explain in this post, is used by most governing bodies, including the FDA.
