Ask the Experts Does research involving retrospective review of patient charts require IRB review? Read More about Does research involving retrospective review of patient charts require IRB review?
Ask the Experts Is IRB review required when linking to clinicaltrials.gov postings on patient advocacy websites and newsletters? Read More about Is IRB review required when linking to clinicaltrials.gov postings on patient advocacy websites and newsletters?
Ask the Experts When should a child assent form be used in a pediatric clinical trial? Read More about When should a child assent form be used in a pediatric clinical trial?
Whitepapers Providing Research Participants with New Information: Is “Re-Consent” Always Necessary? Read More about Providing Research Participants with New Information: Is “Re-Consent” Always Necessary?
Whitepapers Informed Consent and COVID-19: An IRB Perspective on Navigating the New Normal Read More about Informed Consent and COVID-19: An IRB Perspective on Navigating the New Normal
Ask the Experts What documentation is needed to prove a parent’s legal authority to consent for a child’s participation in research? Read More about What documentation is needed to prove a parent’s legal authority to consent for a child’s participation in research?
Ask the Experts What are the signature requirements for translated informed consent documents? Read More about What are the signature requirements for translated informed consent documents?
Ask the Experts Questions on regulations for process development and purchased human cells Read More about Questions on regulations for process development and purchased human cells
Ask the Experts How to resolve irregularities in the documentation of informed consent? Read More about How to resolve irregularities in the documentation of informed consent?
Ask the Experts What elements of Informed Consent must we include when pre-screening? Read More about What elements of Informed Consent must we include when pre-screening?