On-demand Webinar
Didn’t Expect That to Happen: Events That Must be Reported Promptly to the IRB
After a new study is approved, researchers must promptly report certain events to the institutional review board (IRB) for evaluation. This is in addition to required notifications to other entities, and managing these various reporting obligations can sometimes be complicated.
In this webinar, find out what needs to be reported to the IRB. A discussion of example scenarios helps illustrate how to evaluate potentially reportable events.
Learning Objectives:
- Explain why reporting to the IRB is necessary
- Describe the impact of under- and over-reporting
- Identify the types of events to promptly report to the IRB
Lauri Carlile
MS, CIPChief Research Services Officer
Tom Closson
BS, RPh, CIPVice President, Global Review Services
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.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.
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