The Changing Role of the CRA in an RBM World

The changing role of the CRA in an RBM world

The Changing Role of the CRA in an RBM World

Approximately a third of clinical trials conducted utilize some elements of Risk Based Monitoring (RBM), with this figure expected to increase. Site monitoring has been identified as one of the largest components of clinical trial expenditure. With the change in the way that site monitoring is performed, the role of the Clinical Research Associate (CRA) […]

Read More

December 28th, 2016
Real time access to data

Clinical Trial Performance is Improving with Real Time Access to Data Intro

Over the years, technology within medical research has advance enormously, improving its methods of inputting and capturing data. When conducting clinical trials, it is crucial that current data is available throughout the study so that informed decisions can be made from start to finish. Electronic data capture (EDC) systems manage digital data from various channels […]

Read More

December 11th, 2016

Add George Clinical to your network