Director EMEA, Consulting Services
Adrian is EMEA Regional Director Consulting Services at NAMSA, responsible for Biosafety, Medical Writing, and Regulatory and Quality Services. He utilises his broad experience of the changing EU medical device regulatory requirements to support clients worldwide. He was previously Head of Notified Body for the UK Notified Body SGS. Prior to that he was Global Clinical Affairs and Regulatory Manager for Medical Devices, with responsibility for conformity assessment activities of high risk (class III) devices under the Medical Device Directive.
He has 26 years experience in the industry and in this role combines his experience from new product development with EU regulatory requirements to provide a balanced interpretation of the needs and expectations of both competent authorities and manufacturers. He works with a broad range of devices including drug-device combination products.
Monday, September 23
2:05 PM – 3:00 PM