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Compliance and quality assurance are essential during clinical trials. Learn how you can streamline your clinical organization’s content from Site Start Up to Regulatory Submissions and add value to your organization by increasing efficiency, providing security controls, and facilitating collaboration all while maintaining compliance.

The discussion will include:
  • Best practices for managing essential content collected during a clinical trial
  • Ways to streamline the implementation of your enterprise content management system
  • Innovative solutions for Clinical Content Management
  • Best practices for vendor selection for your content management needs
  • Live Q & A session
About the Presenters:
Erin Northington
Erin Northington

Vice President of Emerging Life Sciences Erin has two decades of experience in Clinical Applications, Business Relationship Management and Project Management. She also has a background in GCP compliance, vendor evaluation and management, systems validation and implementations, as well as process evaluation and improvement. She specializes in managing global enterprise-wide IT implementations of technology solutions.

Manu Vohra
Manu Vohra

Managing Director, Life Sciences at Box Manu is the global lead for life sciences and go-to-market strategies for Cloud Content Management at With two decades of deploying ECM solutions in a regulated industry, he supports life sciences companies riding the digital transformation wave to fully leverage the micro content services provided by Box.

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