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Siobhan Ashmore has over 25 years of International Experience in the Pharmaceutical, Medical Device, Biopharmaceutical Industry.  Siobhan has vast experience as an auditor with 15 years in Manufacturing Validation, Quality, Regulatory Compliance Management positions, 7 years as a Consultant QA Auditor. She has led Inspection Readiness Teams for organizations globally during FDA, TGA, EU Regulatory Audits.  Siobhan is on the Audit Board of the American Society of Quality (ASQ).  She is currently involved in supporting organizations in their Software Validation and Software Supplier Evaluation activities for GxP processes. Her passion is supporting organizations in their “Inspection Readiness” endeavors. She is a proud ambassador of the CAI Audit App developed to streamline Inspection Readiness activities.