At Qserve, we take pride in our team of experts who support global registrations for medical devices in various countries. Today, we are happy to introduce you to Joshua Spencer, Literature Searches and Reports Expert, who has recently transfered from the IVD-team to the Global Registrations Team.
Joshua first joined Qserve in early 2021 as a member of the IVD team. In this role, he was primarily responsible for conducting high-quality, systematic literature reviews for a wide range of IVD manufacturers. His work involved planning and strategy development, literature searching, critical appraisal, and the preparation of detailed reports to be implemented into a clients PEP/PER.
A New Challenge
In mid-2024, he began supporting the Global Registrations Team; specifically relating to services as a UK Responsible Person. As of late 2025, he has become a fully dedicated member of the team. In this position, his work centres on reviewing, processing, and validating client documentation to ensure the compliant registration of medical devices and IVDs for the UK market.
When we asked Joshua about his experience in the new team, he answered:
"Working closely with the Global Registrations Team has broadened my perspective on the medical device and IVD regulatory landscape, aligning closely with my academic focus, as I am pursuing an MSc in Medical Device Regulatory Affairs. I am motivated to combine this growing regulatory knowledge with hands-on registration services and handling increasingly complex regulatory inquiries - an area of rising importance in today’s rapidly evolving regulatory environment".
A Valuable Member to Our Team
With his attention to detail, strong organisational skills, and broad regulatory expertise, Joshua is a valued and trusted member of the Qserve team. Need extra regulatory capacity or expert support tailored to your needs? Discover how Qserve's flexible way of working can seamlessly strengthen your team. Get in touch with us today!