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Rethinking the Need for “Signatures” in EDC Systems
Is there a more secure way to review and approve the data that’s collected on case reports forms? In this post, we examine the value and purpose of the traditional signature used in an EDC system.
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Clinical Trial Data Storage Requirements: What Sponsors Need to Know
What should research teams take into consideration when evaluating a data collection and study management solution’s storage capabilities? In this post, we take a look at different elements of database storage and how they apply to clinical trials.
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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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Why Do Clinical Trials Cost So Much? Looking Beyond the Obvious
EDC is no exception to the high costs associated with the healthcare industry. And as technology continues to evolve, researchers need an EDC that will keep pace with the rest of their tools. TrialKit is one system that provides an overdue solution to begin attacking unnecessary high costs at their point of origin.
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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.
