Meghan Hosely

Achieving diversity, equity, and inclusion in clinical trials is vital for inclusive data, safe treatments, and addressing community-specific needs.

Assessing feasibility in clinical research is vital for success, enabling organizations to make informed decisions and ensure seamless execution and reporting of studies.

This checklist offers a comprehensive framework for managing all necessary essential regulatory documents efficiently.

It’s important to define what falls into training and what doesn’t. The key is to know what the training is intended to accomplish.

Navigate the ever-changing landscape of innovation and technology in clinical operations by discovering strategies to help your organization.

As technology evolves and the industry streamlines research workflows, implementing SSO can lead to significant improvements in both user experience and security.

Learn how to optimize clinical trial initiation with centralized processes, intuitive intake forms, and custom reporting and streamline workflows for efficiency.

Explore the transformative power of eSource in clinical research, streamlining data collection for efficiency and cost savings.

Clinical research professionals provide relevant insights into challenges and barriers impeding study start up.

A robust corrective and preventive action (CAPA) stands as a critical tool for proactively addressing deviations in clinical research.

Understand the significance of HRPP staffing despite an sIRB mandate, and how HRPP staffing maintains ethical research practices.