Real Regulatory to attend Medical Technology UK 2023
The UK’s only event exclusively focused on the design, development and production of medical devices. Serving the needs of device OEM’s their engineers, supply chain managers and senior executives.
Our colleague Catherine Partington will be in attendance. Real’s committed experts have a proven track record in all aspects of medical technology. We will work with you to design and implement a competitive and cost-effective regulatory strategy, prepare and submit a comprehensive technical file/design dossier application and act as your intermediary with the notified body or regulatory authority.
We would welcome the opportunity to meet with you and discuss your needs.
To arrange a meeting at a time convenient to you, contact us today.
Catherine has worked in Quality Assurance since 1987 then, in 1993, began to focus on Regulatory Affairs for medical devices. She has worked for companies with manufacturing in Europe, US and Asian markets covering many categories of medical device and other product portfolios from orthopaedic implants, first aid and wound care, consumer healthcare and aesthetic devices. CE marking medical devices from Class I through to Class III, cosmetic products, non-medical electrical devices along with completion of regulatory submissions and approvals in many international markets.
Working on all aspects of regulatory device submissions, under both MDD and MDR including product development, product changes, vigilance, post market surveillance, ISO 13485, MDSAP, KGMP, BGMP, Taiwan QSD.
