Dr. Joachim Maus

... including responsibility for Global Drug Safety (Pharmacovigilance)

Global Responsibility (including China and Japan) for Clinical Operations, Biometrics, Data Management and Programming, Clinical Pharmacology, Clinical Strategy & Innovation, and Clinical Sciences.

Global responsibility for clinical development strategy for Viatris' generics, complex generics, biosimilars, branded medicines, and over-the-counter consumer products including geo-expansion, and life cycle management (LCM).

Directing about 200 people in Global Scientific Affairs incl. corp. functions of Clinical Dev., Pharmacovigilance, Drug Regulatory Affairs, Pharmaceutical Dev. & Quality Assurance with hub in the US and corp. centers for medical devices & cosmetics/food supplements in Italy. Wordwide medical & drug safety responsibility. Global development and registrations e.g. of inhaled, intranasal,dermatological or pain products Inventions of medical use patents Restructuring and integration of acquired companies

Europäische Verantwortung für Clinical Research, Drug Safety und Statistics & Market Access.

Verantwortlich für alle klinischen Studien (Phase I-IV)

Verantwortlich für Phase I Einheit mit Labor

Stationsarzt in Innerer Medizin mit Notaufnahme und Intensivstation, Schlaflabor, Teilnahme an klinischen Studien