Regulatory
Clinical Trial Safety
What are IRB submission requirements for post marketing safety reports?
Blog Posts
Ethics in Clinical Research
May I pay a physician for referring a patient to our study?
Blog PostsInstitutional Biosafety Committee Review for Genetically Modified Vaccines and Gene Transfer Products
VideosCOVID-19 Ethics: Looking at Data Dissemination, Vaccine Development and Access to New Therapies Through an Ethical Lens
Videos
Clinical Trial Safety
Submitting Deviations from a Sponsor’s Adverse Event Reporting Requirements to the IRB
Blog Posts
COVID-19
Informed Consent: An IRB Perspective on Navigating the New Normal
Blog Posts
Series: Ask the IRB & IBC Experts
What documentation is needed to prove a parent’s legal authority to consent for a child’s participation in research?
Blog Posts
COVID-19
IRB Experts Offer Advice for Changing Research Landscape
Articles
Hybrid & Decentralized Trials
What are the regulations for training home health individuals who are working remotely to collect study data?
Blog Posts
Series: Ask the IRB & IBC Experts