Formycon AG
Florian Strohmaier is an accomplished regulatory affairs and quality management professional with extensive experience in the biopharmaceutical sector. Currently serving as Vice President of Regulatory Affairs and Quality Management at Formycon AG since December 2015, Florian leads the development of global regulatory strategies for biosimilar projects and oversees compliance activities. Prior roles at Formycon include Director of Regulatory Affairs and Quality Management and Director of Regulatory Affairs, where responsibilities encompassed establishing the Regulatory Affairs Department and coordinating health authority interactions. Florian also held senior positions at Acino Pharma AG and Sandoz Pharmaceuticals, focusing on regulatory strategy, health authority submissions, and project management for biosimilars. Education includes a Master of Drug Regulatory Affairs from Rheinische Friedrich Wilhelms Universität Bonn and a Diplom in Biotechnology from Fachhochschule Weihenstephan Freising.
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Formycon AG
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Who we are Formycon is a leading, independent developer of high-quality biopharmaceutical medicines, especially biosimilars. The company focuses on treatments in ophthalmology, immunology and on other key chronic diseases, covering the entire value chain from technical development to the clinical phase III as well as the preparation of dossiers for marketing approval. With its biosimilars, Formycon is making a major contribution towards providing as many patients as possible with access to vital and affordable medicines. Formycon currently has four biosimilars in development. Based on its extensive experience in the development of biopharmaceutical drugs, the company is also working on the development of a COVID-19 drug FYB207 About Biosimilars: Since their introduction in the 1980s, biopharmaceuticals have revolutionized the treatment of serious diseases such as cancer, diabetes, rheumatoid arthritis, multiple sclerosis and eye diseases. In the coming years, many of these biotech drugs will lose their patent protection – and by 2020, medications with revenues of approximately USD 100 billion will be off patent. Biosimilars are follow-on versions of biopharmaceuticals, for which exclusivity has expired. They are approved via stringent regulatory pathways in highly regulated markets (such as EU, US, Japan, Canada, Australia) based on proven similarity of the biosimilar with the originator biopharmaceutical reference product. Global sales of biosimilars are estimated to exceed $15 billion by 2020. By 2030, analysts estimate that this figure could rise to over $60 billion. Contact: Formycon AG Fraunhoferstr. 15 82152 Martinsried/Planegg Germany phone +49 (0) 89 - 86 46 67 100 fax + 49 (0) 89 - 86 46 67 110 info@formycon.com