Ulrich Granzer

Ulrich is the founder and owner of Granzer Regulatory Consuting & Services and has more than 25 years of experience in drug development and regulatory affairs. He has held senior management positions at Glaxo as Director of Regulatory Affairs and was a member of Glaxo Wellcome's Global Regulatory Board.

Ulrich has broad experience in drug development including oligonucleotides. At BASF Pharma he served as Vice President of Global Regulatory Centres, assuming global responsibility for Regulatory Affairs, Drug Safety, and GXP in drug development. At Knoll he was responsible for the development of small molecules as well as several biological compounds in the indications of obesity, stroke, septic shock, and rheumatoid arthritis.

He was instrumental to the program for the first fully human anti TNF antibody, now marketed as Humira. Before starting his own consultancy in 2002, he joined Bayer as Vice President of Global Regulatory Affairs, whose responsibility extended over all regulatory aspects of development and submission projects worldwide.