Compliance and quality assurance are essential during clinical trials. Learn how you can streamline your clinical organization’s user acceptance testing of IRT, EDC and ePROD systems and add value to your organization by increasing efficiency, providing security controls, and facilitating collaboration all while maintaining compliance.
The discussion will include:
- User acceptance Testing best practices
- Systems Standardization
- USDM UAT solutions
- Live Q & A session
About the Presenters:
Erin Northington, Vice President, Clinical Services and Solutions, USDM Life SciencesErin 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.
Scott Hatlestad, Director, Clinical Services and Solutions, USDM Life SciencesScott has over 20 years of experience in IT, Quality Systems, Auditing and CSV. He has Extensive knowledge of EDC, IRT and ePRO system utilized in the clinical space. Experience is balanced between business analysis, process improvement, validation, vendor audits and system design roles. Scott has facilitated UAT on systems for over 200 clinical studies.