Principal Investigator
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
Clinical Endpoints
People, Process and Technology: The Right Combination for Successful Expert Committees
Podcasts
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
Should Consent Form updates be aligned with Investigator Brochure updates, or wait for next Protocol amendment?
Blog Posts
Technology
Best Practices For Delivering Investigator Training Via Virtual Meetings
Blog Posts
WCG’s WIRB-Copernicus IRB Announces New Program to Facilitate IRB Review of Research Protocols for COVID-19 (Coronavirus) Vaccines and Therapies
News
Clinical Endpoints