Louise is qualified person & quality control manager at CellGENTherapies. Her critical thinking and decision making is an important asset for the GMP processes and activities.

She is overseeing the GMP-compliant manufacturing of cell- and gene therapies for phase I/II clinical trials, as wel as the GMP-compliant production process for personalized mRNA vaccines, covering the full workflow from qualification of starting materials to quality control of the final drug product.

As a pharmacist, she is bringing to CellGENTherapies several years of industry expertise as quality engineer at Pfizer’s Puurs, focusing on quality assurance within a GMP-regulated production environment.