Chantal completed her pharmacy study in Groningen in 1991. For several years she worked as auditor and QA expert in the Quality Assurance department of a Clinical Research Organization (CRO) and got very familiar with GCP, GMP and GDP systems. At the same time she was responsible for the storage (as responsible person) and packaging (as head of production) of investigational medicinal products (IMPs).
Chantal joined BFC in 2002 and acts as responsible person (RP) and qualified person (QP) for several pharmaceutical distribution, manufacturing and importing sites, also performing batch certification for the market. She performs license support (application and maintenance of wholesale, manufacturing, opiate and import license) e.g. for companies setting up a new supply chain in The Netherlands. She worked on QA projects regarding design, implementation, maintenance and auditing of quality systems (GDP and GMP) as well as executing clinical research projects and various regulatory affairs (RA) projects. Besides, Chantal has a recognition by the FAGG (BE) as Person Responsible for Information and Publicity (RIP).