Watch: Best Practices for Multicenter Research Management with Technology

Learn best practices, tips, and tricks for managing multicenter clinical trials with technology.

Multicenter research introduces unique challenges and bottlenecks for clinical trial leaders who are expected to manage studies across sites.

To avoid study delays and compliance risks when managing multi-site trials, leaders must prioritize maximizing operational efficiency while ensuring inspection readiness and oversight.

In this recorded webinar learn how coordinating centers conducting multi-site research are harnessing technology to:

  • Eliminate operational inefficiencies and compliance risk
  • Streamline site communication and document exchange
  • Access real-time site progress dashboards
  • Standardize document workflows and naming conventions across sites
  • Automate and digitize processes that were once done on paper
Watch Recording

Ensuring your eRegulatory/eSource solution is flexible for your needs is essential to maximizing the benefits of this innovative technology.

eRegulatory and eSource Capabilities Covered

  • Project Management Capabilities

  • Document Management Capabilities

  • Alert and Reporting Capabilities

  • Document Editing Capabilities

  • Platform Compliance with FDA Regulations

  • Access and Permission Capabilities

  • Integration Capabilities

  • Implementation and Support

eRegulatory and eSource Capabilities