Med/Sci
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
COVID-19
Part 3: Evaluating Study Status and Leveraging Data Monitoring Committees to Make Study Decisions
Whitepapers
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