What Happens When a Study Fails to Meet Its Recruitment Targets?
When reviewing research, should IRBs consider the ability of researchers to hit their stated enrollment targets?
IRB review helps ensure risks to clinical trial participants are reasonable and appropriately minimized. But if resources are insufficient to hit enrollment targets (or inclusion criteria so tight it reasonably precludes full enrollment), then are risks really minimized?
Join this webinar for a thought-provoking discussion of why studies don’t meet enrollment targets and what IRBs might do about it.
Summarize the regulatory criteria for IRB approval
Describe how low enrollment might fit into IRB responsibilities
Identify ways to overcome the most common enrollment barriers
MCSE, CIP, CPIA, CRQM
Senior Vice President, Global Review Operations
Senior IRB Chair Director
Senior IRB Chair Director, Advarra
Who should watch?
This content applies to IRB professionals involved in reviewing research and overseeing IRB activities. It also applies to research professionals representing sponsors, CROs, and institutions who are involved in the planning, development, and execution of clinical drug and device trials.
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
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DATE: June 17, 2021
Time: 1 pm ET | 10 am PT
Duration: 1 hour