Sally is a UK-trained medical doctor with over 20 years of international experience spanning clinical anaesthesia, medical device regulatory affairs and laboratory management. She specialises in EU MDR clinical strategy and is an experienced medical writer in Clinical Evaluation Reports (CER) and PMCF planning, writing and review. 

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Having worked as a clinician, medical device entrepreneur and consultant, Sally brings a valuable perspective that connects manufacturer, regulator and end-user needs. She works closely with regulatory and clinical teams to develop robust, practical strategies aligned with Notified Body expectations. 

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