Tom is an experienced regulatory and quality consultant specialising in medical devices and in vitro diagnostics (IVDs). He helps manufacturers — from innovative start-ups to global organisations — navigate complex regulatory frameworks and implement effective quality management systems.

With deep expertise in ISO 13485, MDR, IVDR, MDSAP and UK MDR requirements, Tom provides practical, regulator-informed advice that enables companies to achieve and maintain compliance without unnecessary overhead. He has supported organisations through QMS audits, technical documentation development, clinical and performance evaluations, and regulatory submissions across UK, EU, and global markets.

In addition to consultancy, Tom acts as an outsourced PRRC (Person Responsible for Regulatory Compliance) and UKRP (UK Responsible Person), giving clients trusted oversight and a reliable regulatory presence in the UK and EU. He is also experienced in guiding manufacturers through the challenges of drug-device combination products under Article 117.

Passionate about turning compliance into a growth enabler, Tom partners with clients to strengthen their systems, accelerate market access, and free up teams to focus on innovation.