Interactive Speaker

Catherine Holzmann has worked in the in vitro diagnostic medical devices field for over 30 years and is currently the In Vitro Diagnostics Medical Device Department Manager of the Medical Devices Certification Division of GMED, a position she has held since 2006.
She began her career as a Marketing Manager at Sanofi Diagnostics Pasteur and then lead her career to Regulatory Affairs position at Bio-Rad Laboratories. She was graduated Doctor in Pharmacy in 1985 and received a PhD from internship in Biology in Paris in 1989.
Catherine is a qualified QMS Lead Auditor, Product Reviewer and NBCG co-chair.