Join the session using this link: ZOOM LINK
Objectives
After participating in this educational activity, attendees should be able to:
1| Locate IRB-specific forms and documents and set up IRB Net profiles, including linking CITI Training and CVs to studies and obtaining required signatures.
2| Explain the purpose of external and ancillary reviews, including the Scientific Review Committee, Information Security Reviews, Unaffiliated Investigator approvals, COI review process, and Data Use/Data Transfer Agreement approvals.
3| Determine when and how to submit less common submission types, including Unanticipated Problems, Reportable Events, Decedent Research Forms, Emergency Use Research, and Prep to Research submissions.
Presenter(s):
Lauryn Esposito, CIP
IRB Reliance Analyst
Baystate Health
Michael Boland
IRB Coordinator
Baystate Health
| Name | Role | Financial Relationship Disclosures | Discussion of Unlabeled/Unapproved Uses of Drugs/Devices in Presentation? |
|---|---|---|---|
| Lauryn Esposito, CIP | Speaker/Author | No relevant relationships with ineligible companies to disclose | no |
| Michael Boland | Speaker/Author | No relevant relationships with ineligible companies to disclose | no |
- 1.00 AMA PRA Category 1 Credit™
- 1.00 ANCC Contact Hours
- 1.00 BCIPE Risk Management
- 1.00 IPCE Credit Hour(s)
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