Gentiane Verstraeten, IGR MRQA

As a specialist in quality management, Gentiane Verstraeten has a strong scientific background and more than 20 years experience across many disciplines in the pharmaceutical industry. This experience is used to provide a broad range of consulting services. Mrs Vertraeten can assist you in evaluating risk assessment around GxP processes. She has proven leadership skills involving managing, developing and motivating teams to achieve their objectives.
Mrs Verstraeten 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 in helping to develop and implement 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, Mrs Verstraeten gained experience in the evaluation of Chinese clinical trials and Belgian pharmacovigilance inspections. She is member of the BARQA Association (British Quality Assurance Association).