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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

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 is a seasoned professional with two decades under his belt deploying content management solutions for Life Sciences while running operations within several IT functions supporting Drug Discovery to Commercialization. He specializes in guiding Biopharmaceuticals in developing long term content management strategies by applying Digital Transformation principles and technologies.

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