Raw Material Compliance in Pharmaceuticals: Naming, Pharmacopeial Grade, and Safety Requirements
Stef Schutte
02 Dec, 2025
With 30+ years in pharma, Stef has led global Regulatory Affairs at Astellas and served as Head of RA-EMEA at Merck (MSD), advancing development, approvals, and compliance across international markets. Extensive experience in strengthening regulatory operations, accelerating product development pathways, and building high-performing teams.
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