gained experience in the pharmaceutical industry for over 35 years in various management positions; including quality control, project management, regulatory affairs, pharmaceutical development and quality assurance. During a three-year assignment abroad in India, he set up a pharmaceutical development centre as a greenfield project.
Since 2016, he has been supporting pharmaceutical companies as a consultant in issues related to regulatory affairs, development, quality assurance and as a QP. Due to his wide-ranging professional activities, he is also familiar with the challenges at the various interfaces. Dr. Vigenschow was a lecturer at the DGRA Master of Drug Regulatory Affairs course for many years and is still a speaker at many public and in-house seminars.