On-Demand Webinar

Simple Ways to Uncover Research Compliance Blind Spots

Research compliance professionals routinely confront emerging complex and uncertain situations. Questions often arise about improving informed consent compliance, addressing the weightier compliance risks throughout institutions, or increasing the chances a new compliance initiative might succeed. But the most challenging of compliance entanglements are all too often unexpected and imperceptible: Research compliance professionals haven’t even realized they should have been paying attention, or why. The reason: blind spots. In this webinar, Draco Forte and David Staley of Advarra offer three strategies to check and reduce blind spots regularly to improve compliance oversight.

Learning Objectives:

  • Outmaneuver complex situations by learning to identify blind spots in areas of research compliance
  • Study a scenario and use prospective hindsight to navigate potential pitfalls in best practice thinking and avoid jumping prematurely to noncompliance
  • Identify ways to test implicit compliance assumptions

Presented By

David Staley

MA

Associate Director, Institutional Research Center of Excellence
Advarra

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Draco Forte

M.Ed., CHRC

Associate Director, Institutional Research Center of Excellence
Advarra

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Who should watch?

This content applies to operational staff, including leadership, from academic medical centers, cancer centers, and health systems.

CE Credits

Attendance at this session has been approved for 1.00 contact hour of research specific continuing education on applications for Maintenance of ACRP’s CCRC®, CCRA®, CPI®, or ACRP-CP® certification designations.

Provider approved by the California Board of Registered Nursing, Provider Number 17600, for 1 contact hour. This documentation must be retained by the licensee for a period of 4 years after the course concludes.

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.

If you would like to obtain CE credits for a different credential, please check with your professional organization to determine if our webinars meet their continuing education 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: March 24, 2022
Time: 1 pm ET | 10 am PT
Duration: 1 hour

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