Dympna Starling

ICR

Biography

Dympna Starling is an experienced practitioner in Quality, Audit and Compliance.  Following an early career as a Pharmaceutical Microbiologist in a GMP facility, Dympna moved into QA and has worked in Clinical Trials, Phases 1-4, for over 25 years. As an independent consultant Dympna now supports pharma and biotech clients with quality management system development, training, sponsor oversight, vendor audit and inspection readiness. 

She has many years of experience in preparing for and hosting regulatory inspection in Europe and North America, including pre-approval inspections by EMA and FDA inspectors at clinical sites.  

Dympna holds a Master’s in Biotechnology, and a Batchelor of Science in Microbiology from University College Galway. She is eligible to be an QP for IMPs.