With over 18 years’ experience in clinical research, Chris has worked across both pharmaceutical and medical device sectors. With a clinical background, he’s spent much of his career working with implants, critical care technologies, and a wide range of medical devices. 

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Along the way, he’s built strong expertise in medical writing, MDD to MDR transition, and clinical regulatory compliance, giving him a solid understanding of the requirements and guidelines that shape clinical evaluation and medical devices. 

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Chris has also developed skills in ISO 14155 Good Clinical Practice (GCP) auditing, allowing him to support and assess clinical trials to ensure they meet international quality standards as required by EU MDR 2017/745.

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