Peter Embley

Peter brings over 19 years applied industrial and commercial biopharmaceutical experience to his role, including seventeen years in Regulatory Affairs; working within the Generic, R&D and CRO industries. Peter has a strong grounding in EU legislation and filing strategies and has developed both regional and global strategic perspectives coupled with commercial acumen and experience working within multicultural project teams.

Peter’s collective experience reflects a balance of regulatory experience in Drug Development and Lifecycle Management. He has managed several ANDA applications during his time at Ranbaxy (circa 2007), and trained/mentored regulatory inductees, in the US/EU generic submission process at Chugai, Ranbaxy and PPD.