Horst Kastrup has a background of more than 35 years in regulatory affairs, pharmacovigilance, and
quality assurance. He started his industry career at Wyeth in Germany in 1982, and was promoted to
Head of Global Regulatory Affairs in 1990. In 1998, he took over responsibility as Head of Regulatory
Affairs and Pharmacovigilance at ASTA Medica in Frankfurt, whose Viatris branch was acquired in 2005
by the Swedish Meda group. In 2005, corporate quality assurance was added to his responsibilities.
Since 2010, he is Senior Regulatory Advisor at Meda Group. Both at Wyeth and ASTA/ Viatris/ Meda,
the labelling/ artwork department was part of the Regulatory Affairs organisation and reported to him.
Additionally, Horst Kastrup is a lecturer at the University of Bonn for the Master of Drug Regulatory
Affairs (MDRA) course.
Check out the incredible speaker line-up to see who will be joining Horst.