MEET THE TEAM
Our team of Associate Consultants bring together expertise across regulatory affairs, clinical evaluation, biocompatibility, and post-market activities. We understand the level of detail, accuracy, and judgement required - and we apply that knowledge carefully to every project we support.
Just as importantly, we understand the pressures you’re working under. Regulations evolve, expectations shift, and timelines can be tight. That’s why we stay closely aligned with the latest guidance and regulatory thinking, so you don’t have to navigate it alone.
We work alongside you as a trusted partner, helping you make sense of complex requirements and move forward with clarity. The goal is always the same: to provide clear, reliable support that helps you meet your obligations with confidence.
Chris Hands
As Founder and Principal Consultant of Hands on Research, Chris brings over 18 years of experience in the medical device industry. >
Emma Hyland
Emma is an experienced Medical Writer specialising in Clinical Evaluation Reports. She holds an MRes in Clinical Sciences, with expertise in critical appraisal and EU MDR compliance. >
Kelsey Roberts
Kelsey is a regulatory affairs leader with 9+ years’ experience driving global medical device strategy and delivering an exceptional number of FDA 510(k) clearances. >
Chris Jenkins
Chris holds a BSc in Biotechnology and has over 15 years’ experience in the medical device industry, with deep expertise in pharmaceuticals and combination products. >
Sally Sennitt
Sally is a Medical Doctor with 20+ years' experience in anesthesia, regulatory affairs, and laboratory management. She has a MSc in Medical Device Regulatory Affairs. >
James Allard
James is a regulatory specialist with 18+ years’ experience supporting EU MDR strategy, technical documentation, and quality systems, holding a PhD in Organic Chemistry and MSc. >