Criteria for IRB Approval - Essential Training for IRB Members and Staff 2018 is a webinar that covers topics such as:
- Important definitions every IRB administrator/member must know
- Applicability of HHS and FDA regulations for the protection of human subjects
- IRB`s role to determine that risks are reasonable in relation to anticipated benefits
- How to identify and minimize potential risks in a research study
- Focused review of the criterion for obtaining legally-effective consent
- IRB`s review of protocols to ensure equitable selection of subjects
- IRB review of safety monitoring plans
- When and how to require documentation of informed consent for different types of studies
- Consideration of additional safeguard for the protection of vulnerable subjects
- How to protect confidentiality of research data and minimize potential breaches of confidentiality
Criteria for IRB Approval - Essential Training for IRB Members and Staff 2018 is intended for:
- IRB Administrators
- IRB Members
- IRB Managers
