Giselle Bates

The concept of EDC (electronic data capture) systems in clinical trials was first introduced over two decades ago. However, these archaic legacy systems are in no way equipped to deal with the sheer...

Code, libraries, configurations, open source and proprietary binaries, container dependencies, and plugins are all components of the software supply chain. Build servers, assemblers, compilers, source...

In the realm of medical research, the efficiency and accuracy of managing documents are paramount to the success of clinical trials. Document Management Systems (DMS) have emerged as indispensable...

Clinical trial complexity has grown in both size and breadth, from small rare illness studies to massive vaccination trials with tens of thousands of patients. However, not all electronic data capture...

Understanding the variety of KPIs that a CTMS may create is critical as the biotechnology and pharmaceutical sectors increasingly rely on Clinical Trial Management platforms. These systems provide a...

In the rapidly evolving landscape of healthcare, the management of clinical trial data stands as a linchpin in advancing medical research and innovation. Within this dynamic sphere, the convergence of...