At Qserve, we take pride in our team of experts who support global registrations for medical devices in various countries. Today, we are pleased to introduce you to Mendy Belt, one of our Global Registration Specialists with expertise in Vigilance Reporting and Post-Market Surveillance.
Mendy joined Qserve in July 2025 as part of the Global Registrations team. Her key focus is supporting the UK Responsible Person (UKRP) service, helping non-UK manufacturers bring their medical devices to the UK market.
Mendy has an educational background in Nursing and successfully completed the Bachelor of Arts at the University of Groningen. Before joining Qserve, she spent nearly 10 years in the United Kingdom, working for a global medical device and in-vitro diagnostics manufacturer. During this time, she gained valuable experience in customer quality, including complaint investigation, global vigilance reporting, sustaining PMS activities (e.g. preparation of PMS reports, PMPFs and PSURs) and post-launch risk monitoring.
Throughout her career, she has consistently proven to maintain a high standard of performance by complying with regulatory requirements and internal processes, working with accuracy whilst adhering to deadlines.
At Qserve, Mendy is responsible for the submission of documentation for the registration of Medical Device and IVD companies and their products for worldwide market access. She maintains contact with the clients and collects the relevant documentation to build registration files. She manages the full registration process through communication with local competent authorities, ensuring that all submission documents are accurate and devices are properly registered in the respective databases (e.g. MHRA database for UK).
With a good knowledge of QMS, ISO 13485, EU MDR 2017/745, IVDR 2017/746, MDSAP and FDA 21 CFR 803/820, complemented by her strong data handling skills, Mendy makes a valuable member of the global registration team.
When we asked Mendy what she enjoyed in her work, she said:
“I’m always excited to grow my personal and business skills and expanding my knowledge. Working with such a wide range of medical devices - and keeping up with constantly changing regulations - definitely keeps me on my toes and makes the work interesting.
I really enjoy being part of a team with people from different backgrounds and cultures. I especially like working directly with customers and supporting manufacturers in registering their devices accurately and efficiently, it’s very rewarding. As every project is slightly different, each one brings a new challenge and an opportunity to learn.”
Our Global Registration Team helps MedTech companies to speed up time to market by providing you with experienced registration capacity. You will always stay up to date with regulatory intelligence and understand requirements, which saves time, reduces risk, and accelerates global reach. Contact us to discover the opportunities!