Paul Sim retires from the Editorial Board of the Journal of Medical Device Regulation

The Journal of Medical Device Regulation (JMDR) bids farewell to one of its founding Editorial Advisory Board members, Paul Sim, as he announces his retirement from the Board. Paul has been an integral part of the Journal since its inception, contributing invaluable insights and expertise to the field of medical device regulation.
Reflecting on his tenure with the JMDR, Paul expressed his gratitude, saying, “I am really grateful to you for allowing me to stay on the Editorial Board of the JMDR and particularly want to thank you for that privilege”.
Victoria Clark, Editor of the JMDR, also extended her heartfelt appreciation to Paul for his outstanding service. “Paul’s dedication and tireless efforts have been invaluable to the success of the Journal. His insightful contributions have greatly enriched our publication and set a high standard for excellence. We are profoundly grateful for his contributions and commitment over the years”.
As Paul embarks on a new chapter in his life, the JMDR extends its best wishes for his future endeavours.
Paul has nearly 45 years’ experience in the healthcare industry. His last role prior to retirement was working as Medical Devices Knowledge Manager – Knowledge, BSI Healthcare. Previously he has held senior RA/QA leadership positions in Spacelabs Healthcare, Teleflex Medical, Smiths Medical, Ohmeda (formerly The BOC Group healthcare business) now owned by GE Healthcare. He has also undertaken regulatory affairs and quality management consultancy through his own SiMedical Device Consulting company.
About the Journal of Medical Device Regulation
The Journal of Medical Device Regulation (JMDR) is dedicated to advancing the understanding and practice of medical device regulation worldwide. The JMDR – founded in 2004 – provides regulatory professionals with in-depth articles on current regulatory matters as well as topical information on international regulatory changes. In addition to publishing review and discussion articles by opinion leaders from the device community, the Journal summarises the global news headlines and provides useful reference information in the form of charts and briefing documents. The Journal is a quarterly, subscription-only publication that is available in electronic format.
For more information on the Journal of Medical Device Regulation, please contact Marija Capek
(tel: +44 7916 443811; email: sales@globalregulatorypress.com) or visit GlobalRegulatoryPress.com.

