Dr. Tilo Netzer

Consulting on regulatory strategies for development, approval and life-cycle management of biotech and other pharmaceutical products

Head of Department Global Regulatory Oncology of the newly formed division for ethical pharmaceutical products (Merck Serono) with staff in Darmstadt/Germany, Geneva/Switzerland and Rockland/USA; additional responsibility as Therapeutic Area Coordinator for all 4 newly formed Therapeutic Areas within Global Regulatory Affairs.

Responsibility for staff in Darmstadt/Germany and Lyon/France; additional responsibility as EU Regulatory Strategy Coordinator with continued responsibility for Erbitux® and Japan strategy coordination for Global Regulatory Affairs

Head of Department/expert role; global regulatory responsibility for cetuximab (Erbitux®).

Regulatory responsibility for all Darmstadt-based oncology/biotech development projects, German marketing authorizations and responsibility for Product Information.