Laura Taylor
Regulatory and Quality Consultant
My name is Laura and I have worked in the medical devices (regulatory and quality) for 10 years. I’ve worked both in manufacturing and, in more recent years, consulting during my career which has covered regulatory affairs, quality management systems and medical writing. I specifically have extensive experience in CE marking, preparing technical files and clinical evaluation reports as well as supporting Notified Body audits and MDSAP audits, as well as other aspects of regulatory affairs. Due to starting my career in orthopaedics, I do have a soft spot for the more manual devices, but I love learning so am always happy to be involved in a variety of devices.
I am happy to share my knowledge with others and increase awareness around medical device regulatory affairs, which is why I am a member of the TOPRA Editorial Board for Regulatory Rapporteur. I also have an MSc in Strategic Quality Management and am a certified lead auditor for ISO 13485
