The need for—and barriers to—adopting eSource

By CenterWatch
Published: April 2018

Electronic data collection responsibility borne by investigative sites to support each clinical trial is onerous, the integration of EMR and eClinical data is making slow progress, with little end in sight. This paper discusses the inefficiencies due to the lack of a standard format for collecting and transferring data, factors contributing to a resistance to change and the implementation of the 21st Century Cures Act.

To learn more, register for our free white paper Envisioning the site of the future.

Please enter in your information below. Fields with an * are required.

Please enter a valid email address to receive an email with a link to download the white paper.   

Please check the types of email communications you would like to receive from CenterWatch:

CenterWatch offers a range of white papers for download that investigate and analyze current trends in the clinical trials industry and the impact they have on the research community.

Recent titles from CenterWatch:

The Research Practitioner Sample Issue

The CenterWatch Monthly Sample Issue

Fastest drug developers and their practices