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Gordon Elger

Senior Advisor at UL Compliance to Performance, USA


Gordon has over 30 years’ experience in pharmaceutical regulatory affairs, research and development across a broad range of European & international regulatory territories. He has been engaged in many types of post approval changes including manufacturing site transfers, Drug Master File updates, new indications and dosing. He masters the aspects of change control procedures in the management of Capa, design dossiers, technical files and other compliance related documentation in instances of relevant and significant compliance and quality deviations issues.

His experience relates to leading regulatory affairs groups of leading life science organizations including Reckitt-Benckiser, Ibsen pharma, Mercury Pharma, Amdipharm Mercury, Wainwright’s associates and most recently as Senior Regulatory Executive at Glaxo Smithkline.

Agenda Sessions