Joseph Irwin is a highly experienced Regulatory Professional with over 25 years in the field of regulatory affairs, currently serving as a Senior Consultant at GreyRigge Associates and a Company Director at both XPforte Regulatory Ltd and LRCS Ltd. They have extensive experience in preparing regulatory submissions for clinical trials, marketing authorizations, and medical writing, specifically in areas like paediatrics, orphan drugs, and complex diseases. Previously, Joseph held roles such as Global Regulatory Lead at CSL Behring and Interim Head of Regulatory Affairs at Diurnal. They earned a BSc in Biochemistry-Pharmacology from the University of Leeds and an MSc in Biomolecular Organisation from Birkbeck, University of London.
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