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PhD in Bio Engineering, MSc Food & Biotechnology, MSc King's College London, MBA Open University, RAC (EU & Global), Chartered Manager, RAPS European Board Member · Division Head Regulatory Affairs
Salma Michor is currently Division Head Regulatory Affairs at the QbD Group. She served clients such as Johnson & Johnson, Novartis, Pfizer and CSL Behring. Previously, Michor worked for Chiesi-Torrex, Wyeth Whitehall Export Croma Pharma GmbH. She teaches regulatory affairs and clinical strategies at the University of Krems, Austria, and is an independent expert to the European Commission.
3 articles
Descubre cómo navegar por el cumplimiento del artículo 117 del MDR para las combinaciones fármaco-dispositivo. Garantiza la correcta aplicación con orientaciones esenciales.
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Build a successful compliance program in pharma by strengthening internal controls and procedures to ensure robust regulatory adherence.
阅读更多Discover how to navigate compliance with Article 117 of MDR for drug-device combinations. Ensure correct implementation with essential guidance.
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