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IRB Training Schedule
Preparing a Successful IRB Submission
Click here to view a recording of Session I
Click here to view a recording of Session II
This training session is designed to guide researchers through the process of submitting
an initial IRB application in Cayuse. Participants will learn how to accurately complete
and submit their study protocol for IRB review. By the end of the session, attendees
will be equipped with the knowledge and skills needed to successfully navigate the
Cayuse platform and submit a complete, thorough IRB application. This training is
ideal for new researchers or anyone unfamiliar with Cayuse.
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Managing Modifications, Incident Reports, and Closures in Cayuse
Wednesday, Nov. 6, 2024: 1–2 p.m.
In this training session, participants will learn the essential procedures for managing
study modifications, incident reports, and closures using the Cayuse IRB system. This
interactive session will cover how to effectively submit modifications when changes
occur in a study protocol, report incidents that may impact the safety or integrity
of the research, and formally close a study upon completion. Attendees will learn
how to navigate through Cayuse, ensuring compliance with IRB requirements, and understanding
best practices for maintaining accurate documentation throughout the research lifecycle.
This training is ideal for researchers, coordinators, and administrators involved
in IRB submissions.
*Training will be recorded and available following event.
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Informed Consent: Best Practices
Click here to view a recording
This training session focuses on the fundamental principles and best practices for
obtaining informed consent in human subjects research. Researchers will learn how
to develop clear, comprehensive consent documents that meet ethical and regulatory
standards, and how to effectively communicate study information to participants. Attendees
will gain a deep understanding of the informed consent requirements, and practical
strategies for fostering trust and transparency with study participants. This training
is ideal for researchers seeking to improve their consent process and ensure compliance
with federal regulations.
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IRB Compliance: Avoiding Common Pitfalls
Click here to view a recording
A session that highlights frequent mistakes researchers make in IRB submissions and
compliance, offering strategies for avoiding delays.
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