Meghan Hosely

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.

Having a robust human research protection program (HRPP) in place is vital when maintaining compliance and keeping participants safe.

In a complex and competitive climate, we sought the understand existing perceptions surrounding clinical research trials.

Gain a comprehensive understanding of the various phases involved in clinical research, their objectives, and outcomes that ensure safe and effective clinical treatment.

Discover valuable insights and expert guidance on navigating FDA inspections in clinical research.