Quality Assurance
She has more than 10 years of experience in the techniques (HPLC-DAD, HS-GC-FID, GC-NPD, prep-HPLC…) required for the laboratory analysis of samples from both industry and public health institutions under EPA, FDA, UK, Japanese, ICH, USP, Ph. Eur, GLP/GMP, etc regulations.
Her work experience lies on the determination of pollutants in environmental samples, commonly abused drugs and their metabolites in biological samples, physico-chemical properties in test substances and chemical products, analysis and purification of metabolites to help partners (Astrazeneca, GSK, Abbvie, Lilly, J&J, Gilead, Boehringer ..) in Pharmaceutical succeed and determination of residual solvents and volatile impurities in raw material and medicines.
