Paul Attridge
Paul Attridge, Veeva Systems Europe
Paul leads Veeva’s strategy team for the Vault product in the areas of regulatory and quality. A technologist and business development professional, he has spent the past 23 years in the life sciences industry, following eight years as a software engineer.
Previous roles have included leading the product management function in CSC’s Life Sciences Software Solutions Group. Prior to this, for 14 years he focused on product development, product support, professional services and business development associated with CSC’s Life Sciences solutions, heading up the European Life Sciences organisation during its transition from FCG Inc. into CSC.
Paul Attridge, Veeva Systems Europe
Paul leads Veeva’s strategy team for the Vault product in the areas of regulatory and quality. A technologist and business development professional, he has spent the past 23 years in the life sciences industry, following eight years as a software engineer.
Previous roles have included leading the product management function in CSC’s Life Sciences Software Solutions Group. Prior to this, for 14 years he focused on product development, product support, professional services and business development associated with CSC’s Life Sciences solutions, heading up the European Life Sciences organisation during its transition from FCG Inc. into CSC.
Articles: Paul Attridge
Speeding up Regulatory Submissions Through Continuous Publishing
Opinion / Veeva Systems Europe’s Paul Attridge highlights how a switch to a continuous model for regulatory operations could allow biopharmaceutical companies to submit high-quality regulatory submissions for their products faster than ever before. Like continuous manufacturing, which is widely employed in other industries and is starting to show signs of adoption in life sciences, continuous…
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