Blog
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.
Implementing Risk-Based Monitoring in Your Clinical Trial Processes
Interested in making the transition from traditional site monitoring to a risk-based monitoring model? We shed some light on the topic in this blog post.
Open APIs and Webhooks: The Key to Interoperability in Clinical Research Technology
In this post, we’ll delve into what APIs and Webhooks are, how they function, how they’re being used as an engine for interoperability today.
5 Ways to Make Clinical Trial Recruitment More Patient-Centric
In this guest post from Antidote.me, Nancy Ryerson reveals five insightful tips to create a more patient-centric trial recruitment process.
The Value of Data Collected Using eCOA and ePRO in Clinical Research
Surrounding the industry shift to make clinical trials more patient-centric, there has been a drastic increase in the adoption of eCOA and ePRO solutions. We highlight just a few of their benefits in this post.
The Perfect Form
Crucial Data Solutions’ CEO, Paul Grady, characterizes the perfect case report form and the capabilities your software should have in order to deliver it.
