I have over 35 years of experience in some of the largest innovative pharmaceutical companies in the world, predominantly in Regulatory Affairs CMC, but also in QA/QC and Manufacturing. I built and managed global teams (US, Europe and Japan) of up to 60 employees, and represented the companies I worked for in organizations like EFPIA for many years. I was strategically involved in the Regulatory Affairs leadership team during 2 major takeovers, which has given me much insight in how to deal with change processes. Continuous improvement, six sigma, and competitive advantage are some of the key topics for me as a manager. With the above experience, and based on my knowledge of competitive advantage, change management and project management in general as well as my technical knowledge in the QA/QC and RA environment I am able to provide in depth strategic advice on a wide range of topics in the pharmaceutical industry.