
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.

In this guest post from Antidote.me, Nancy Ryerson reveals five insightful tips to create a more patient-centric trial recruitment process.

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.

Preclinical labs, which have typically relied heavily on spreadsheet-based data collection, are perfect candidates for electronic data capture. Read on for several ways EDC offers improvements to preclinical research.

The TrialKit platform was designed to be simple enough to learn for first time EDC users but sophisticated enough to handle late phase trials and studies with complex sets of data.

TrialKit’s ePRO functionality, now available for download on Google Play, can be easily accessed by clinicians and patients alike from any smartphone or tablet.

Medical coding dictionaries are intentionally maintained and updated over time. As medicine advances, new therapies emerge, safety knowledge expands, and clinical terminology becomes more precise, organizations responsible for maintaining dictionaries such as MedDRA and WHODrug publish regular updates to keep pace. For sponsors and CROs, those updates present an ongoing operational consideration. While current terminology…

Software validation is a major consideration when evaluating tools to aid the clinical research process. This blog post details the questions to ask and things to look for when assessing data collection and study management software.
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.