On-Demand Webinar

Advantages and Considerations for an eRegulatory Implementation

Advarra’s world-class technology solutions and Huron’s research strategy and operations expertise and technologies deliver fully integrated, optimized research workflows for sites. In this collaborative webinar, Huron and Advarra join forces to discuss best practices for eRegulatory (eReg) systems, offering tips for academic medical centers, cancer centers, and health systems.

Experts will highlight key features of an eReg system and considerations to help sites plan for, implement, integrate, and maintain an eReg system within their research technology suite. We will cover topics such as governance and support infrastructure, 21 CFR Part 11-compliance, optimizing your folder structure creation, and maximizing your ROI and adoption rates through integration. Attendees can benefit from the insight of both Advarra and Huron partners and gain a deeper understanding of how to prepare your site for a smooth and successful eReg implementation.

Learning Objectives:

  • Gain an understanding of what an eReg system is and the features available to streamline clinical trial regulatory management
  • Understand the value of eReg to principal investigators, study teams, and compliance officials
  • Learn best practice strategies to prepare for and conduct an eReg implementation
  • Learn how to enhance your return on investment through integration with other research systems
  • Understand the key roles needed for a successful implementation

Presented By


Erin Pennington

Senior Director
Huron Consulting


James Wurdeman

SVP, Technology Strategy and Innovation

Stuart Cotter.png

Stuart Cotter

VP, Product Management

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Who should watch?

This content applies to research professionals representing sponsors, CROs, and institutions who are involved in clinical trial planning, development, and execution.

CE Credits

The Society of Clinical Research Associates (SOCRA - www.SOCRA.org) accepts documentation of candidate participation in continuing education programs for recertification if the program is applicable to clinical research regulations, operations or management, or to the candidate’s clinical research therapeutic area. This program offers 1 hour of CE credit. 

This event may qualify for continuing education (CE) credits. Please check with your professional organization(s) to determine whether the event meets their CE eligibility requirements.

Certificate of Attendance

After watching this webinar in its entirety and completing the webinar survey, you will receive a certificate of attendance. This certificate will be emailed to you within one business day of watching the webinar. Please note that if your organization has other staff members who wish to get a certificate of attendance, each person must register, watch the webinar in its entirety, and complete the webinar survey. Visit our Webinar Help page for more information on certificates of attendance.

DATE: June 17, 2021
Time: 1 pm ET | 10 am PT
Duration: 1 hour

Register Now