A medical device regulatory consultant with a biomedical and mechanical engineering background experienced in the creation and review of technical documentation and QMS, as well as in handling vigilance issues and PMS for a vast array of medical device types and classifications.
John Adcock
CEO – Advena Ltd (UK & Malta)
30 years experience in global medical device regulatory affairs including the position of Vice President of International Regulatory Affairs with…
Andrea Thomas
Regulatory Consultant
A regulatory consultant with an MSc in Medical Statistics with Health Technology Assessment. Experienced in FDA submissions, compilation of CE…
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…