A regulatory consultant with an MSc in Medical Statistics with Health Technology Assessment. Experienced in FDA submissions, compilation of CE technical files and global regulatory submissions, specialising in IVD devices. In-depth understanding of marketing regulations and approaches to IVD verification and validation.
Sarah Pavitt
Senior Regulatory & Quality Consultant
A senior Consultant with over 9 years in medical devices industry working on airways, COPD, IVF and ventilator devices. Responsible…
Purdy Ellul
Business Administrator (Malta)
Over 6 years experienced in Business Administration, Customer Service, Account Management and sales.
Cath Nelson
Regulatory Co-Ordinator
Over 3 years’ experience in Quality Management and Medical Device Regulatory Affairs including Technical Files, Non-EU medical device registrations and…