Criteria for IRB Approval - Essential Training for IRB Members and Staff 2018
05 Jun 2018
Webinar
Description
Topics
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
Who should Attend
IRB Administrators
IRB Members
IRB Managers
Past Events
Criteria for IRB Approval - Essential Training for IRB Members and Staff 2018 - 05 Jun 2018, Webinar (75875)
Important
Please, check "Criteria for IRB Approval - Essential Training for IRB Members and Staff" official website for possible changes, before making any traveling arrangements
Event Categories
Education: Education Technologies & Methods, Training
