E-Book

Our eBook outlines six key areas essential to every site, and provides guidance to help you run your site as a successful business.

Our eBook outlines how eSource can make clinical research data more accessible, accurate, and reliable.

This eBook provides a toolkit to understand the institutional review board's role when sIRB review is utilized.

Many clinical trial sites face challenges to stay compliant on a study. It is important for sites to adhere to the myriad of requirements that constitute Good Clinical Practices (GCP).

How is the research community addressing recent regulatory actions urging improved diversity and representation in clinical trials?

This eBook dives into GCP’s role in the clinical research ecosystem and how it protects participant rights, safety, and confidentiality.

Access the survey report now for current perspectives on study startup activities impacted by rapidly evolving technology and tools.

June 5, 2023

This report defines 2023 clinical research trends and provides an outlook for the industry moving forward.

This eBook shares tips and best practices to guide researchers through the investigator-initiated trial process while staying compliant.

Insights into the site selection process and the information sites provide as part of site feasibility questionnaire completion.

Examine the current state of industry resources, resourcing implications, and the way we can now think of work: remote, hybrid, or on-site.