Randomised controlled trials are the most reliable approach to generate high quality medical evidence. However, protocol specifications and multiple configurations across clinical sites results in inefficient recruitment and execution of the trials. By using the latest advances in eSource and study design models, we aim to provide an integrated electronic clinical trial platform to support the workflow management of clinical studies across different environments found in clinical sites.
Learning Objective: After participating in this session, the learner should be better able to:
Understand the current issues in managing clinical research in primary care across different clinical settings and learn about implemented solutions to increase accuracy and safety when integrating electronic Case Report Forms into routine clinical practice.
Jesus Dominguez (Presenter)
King's College London
Elliot Fairweather, King's College London
Brendan Delaney, Imperial College
Vasa Curcin, King's College London