Regulatory Compliance

CenterWatch | Insights

Can a physician submit a single humanitarian use device (HUD) submission to the IRB?

CenterWatch | Insights

Compensating Research Participants FAQ

CenterWatch | Insights

Do parents need to accompany adolescents at each research-related office visit?

CenterWatch | Insights

When should a child assent form be used in a pediatric clinical trial?

CenterWatch | Insights

Submitting Deviations from a Sponsor’s Adverse Event Reporting Requirements to the IRB

CenterWatch | Insights

What are the requirements for parental permission (consent) in studies involving children?

CenterWatch | Insights

How do I handle a deviation in the use of blood specimens collected outside the timeframe?