Clinical trials rely heavily on robust data collection and management processes to ensure scientific validity and regulatory compliance. While case report forms (CRFs) have traditionally been the ...

Having a clear understanding of where your data is being consumed is a critical first step toward being able to secure and ultimately protect it. Using data flow diagrams, it is possible to know the ...

Sharing of participant-level clinical trial data has potential benefits, but concerns about potential harms to research participants have led some pharmaceutical sponsors and investigators to urge ...