Kick-Start Your Clinical Trial Document Anonymization

Drawing on her academic research background, Niamh has helped develop Privacy Analytics’ CTT methodology and our proprietary toolsets. These toolsets automate many of the more tedious aspects of anonymization so that she and her team can focus their time on delivering higher value service to clients.

Niamh has personally managed many successful projects, with documents representing more than 100 clinical trials, some all the way to publication on the EMA’s Clinical Data Portal. She also led our first dedicated Health Canada PRCI submission. Under her watch, no client has ever missed a regulatory submission deadline or a deadline to make their trial data publicly available.

Today, Niamh shares her expertise in risk-based anonymization of clinical trial documents by attending and presenting at international conferences and forums. Recently, she took a seat on the industry’s Policy 0070 Working Group. The Working Group includes global pharmaceutical companies and other anonymization service providers.

“No matter what deadlines you face or how complex your documents, we can help,” Niamh says. “My team has the experience and the commitment to see that every project is done right. .”