Simone Ferrante

Simone Ferrante is Director Quality at Fisher Clinical Services at the Clinical Trials Division of Thermo Fisher Scientific. In this role, she is committed to ensuring the highest quality standards in clinical research.

She is also an author of specialist literature and practical tools on the subject of GDP for the GMP Verlag Peither. She also shares her expertise as a speaker at the PTS Training Service.

After studying pharmacy, Simone Ferrante was drawn to pharmaceutical logistics. At Grieshaber Logistics Group AG, she introduced a GDP/GMP compliant quality management system and was responsible for its continuous development and implementation.

At the same time, she obtained a Master's degree in Drug Regulatory Affairs at the University of Bonn, which enabled her to deepen her understanding of the legal requirements across the entire life cycle of pharmaceuticals and link these to the responsibilities of a logistics service provider, even before the current GDP guidelines came into force.

She is author or co-author of the following chapter of GMP Compliance Adviser:

0.F Importation of medicinal products

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