Inge Tarnow

I am a drug developer with broad experience from both industry and academia (20+ years) with a comprehensive understanding of scientific challenges and drug development processes. Cross-functional drug development in start-up, scale-up and pharma. Specific experience in nonclinical, translational and bioanalytical development. Core competencies/achivements: - Designed and built the infrastructure of Savara’s drug development project organisation - Acted as strategic cross-functional Project Lead on Molgradex, a multifaceted, international orphan drug development program run by a partly outsourced model - Key advisory role in start-up of clinical phase II/III and phase III trials with an inhaled therapy for a rare lung disease - Key role in interpretation of data and reporting of phase II/III clinical trial including being the main Sponsor participant and driver for a NEJM publication - Leading nonclinical development - selection of CROs, nonclinical regulatory strategy, start-up, conduct and reporting of various GLP tox studies - Identified and overseen strategic initiatives for process and systems improvements within R&D - Led and maintained oversight of R&D data integrity and compliance functions including data governance arrangements

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