A compilation of information, announcements, & updates for UK Institutional Review Board (IRB) members, research investigators, & others involved with human subject research.
New ORI Website Resource for FDA-Regulated Research
Investigators invited to convened IRB meetings are expected to be knowledgeable regarding their IRB submission and prepared to discuss the research protocol. If the IRB is unable to determine that approval criteria are met due to absent or lacking information, the protocol must be tabled, which can delay the review and approval process.
UK Electronic
Research Notebook Webinars
To schedule an event for your team/department/college/center/ institute, please submit a requestand a UK LabArchives team member will contact you promptly.
