Verstraeten

As a specialist in quality management, Ms Verstraeten has a strong scientific background and more than 20 years experience in the pharmaceutical industry from multiple perspectives. This experience is used to provide a broad range of consulting services. She can assist you to conduct risk assessment project around GxP processes. She has proven leadership skills involving managing, developing and motivating teams to achieve their objectives.  She has developed and implemented quality systems integrating different standards and regulations for Pharmaceutical Companies, Contract Research Organization and Non-Profit Organizations. In addition to specific clinical trial audit services (GCP, cGLP, cGMP, DM, CSV, Vendor Qualification and Data Privacy), she can also assist to set up customized training programs , design new Standard Operating Procedures (SOPs) or build quality expertise around medical and promotional communication activities with the aim of improving efficiency across the whole drug development process.
Recently, she gained experience in the evaluation Chinese clinical trials and Belgian inspections. She is member of the BARQA Association (British Quality Assurance Association).