Principal Investigator
Ethics in Clinical Research
What are the requirements for parental permission (consent) in studies involving children?
Blog Posts
What ethical safeguards are needed for research involving observation of group behavior?
Blog Posts
Regulatory Compliance
How do I handle a deviation in the use of blood specimens collected outside the timeframe?
Blog Posts
Questions on the FDA’s 30-Day IND Review Period and IRB Approval
Blog Posts
Series: Ask the IRB & IBC Experts
Is it possible to make a PI’s name or institution confidential on a consent form?
Blog Posts
Clinical Trial Safety
WCG IBC Services
Solution Overviews
WCG Experts to Lead Nine Educational Sessions at the PRIM&R 2019 Advancing Ethical Research Conference
News
Series: Ask the IRB & IBC Experts
What are the Blood Draw Guidelines for Phase 1 Clinical Trials?
Blog Posts
Questions on Using Generic Recruitment Flyers at Clinical Trial Sites
Blog Posts
Site Efficiency