Event Overview:
Scotland’s Medical Device Seminar 2025 will offer you the opportunity for shared learning and discussion on various topics such as new guidance, research outcomes, trial, standard and regulations associated with decontamination of surgical instruments, endoscopes, and primary care instruments.
You will have the chance to learn about new cross-cutting technology and innovation presented by the speakers and the exhibitors.
It also provides you with a space to improve communication and expand your network among a wide range of professionals.
We have a host of dynamic speakers and exhibitors from UK and beyond, who will provide expert insight into the field of decontamination of medical devices.
Who Will Attend:
Registration & Networking
Registration & Networking
Chair Opening Address - (Confirmed)
Chair Opening Address - Dr. Sulisti Holmes, Head of Decontamination and Incident Investigation Reporting Centre, NHS Scotland Assure (Confirmed)
Presentation - Identification and prevention of surface alterations on surgical Instruments caused by waterborne minerals (Confirmed)
Identification and prevention of surface alterations on surgical Instruments caused by waterborne minerals
Synopsis TBC
Presentation - Publications of SHTM 01-05 (Confirmed)
Publications of SHTM 01-05
The development process, main changes and what does it means to dental community?
Presentation - Microbial Contamination of Final Rinse Water for Endoscope Washer Disinfectors (Confirmed)
Microbial Contamination of Final Rinse Water for Endoscope Washer Disinfectors
Q&A
Q&A
Morning Break
Morning Break
Chair Morning Reflection (Confirmed)
Chair Morning Reflection - Dr. Sulisti Holmes, Head of Decontamination and Incident Investigation Reporting Centre, NHS Scotland Assure (Confirmed)
Presentation - Clinical impact of incidents of final rinse water for endoscopes (Confirmed)
Clinical impact of incidents of final rinse water for endoscopes
Synopsis TBC
Presentation - RMD Decontamination Policy and Guidance In NHS Scotland (Confirmed)
RMD Decontamination Policy and Guidance In NHS Scotland
A short overview of new and revised NHS Scotland Reusable Medical Device decontamination guidance.
Case Study - Collaboration to deliver a safe endoscope for every patient
Case Study - Wassenburg
An overview of a customers issues and subsequent actions to resolve those using a collaborative approach with both the customer and third party partners.
Case Study - The hidden risk of build-up biofilm in reprocessed endoscopes
Case Study - Nanosonics
This conference session will highlight the significance of endoscope-associated outbreaks in healthcare, summarising recent literature on endoscope-associated outbreaks and examine build-up biofilm as a root cause. Included will be an overview of current methods and technologies for effective build-up biofilm removal from endoscopes.
Q&A
Q&A
Lunch and Networking
Lunch and Networking
Chair Afternoon Address (Confirmed)
Chair Afternoon Address - Vanda Plecko, Consultant Microbiologist & Infection Control Doctor, NHS Highland (Confirmed)
Presentation - Regulatory Updates from a UK Approved Body (Confirmed)
Updates on changes within UK MDR regulations, and its impact in the healthcare sector.
Presentation - Decontamination Challenges – Pioneering The Future (Confirmed)
Decontamination Challenges – Pioneering The Future
Decontamination, standards, as we know them today, evolved as an industry in the late 1990’s, early 2000’s. Concerns increased regarding the prevention of hospital acquired infections (HAI) and minimising the reduction of the risk of iatrogenic transmission of transmissible spongiform encephalopathies (TSEs), especially the hypothetical risk of variant Creutzfeldt Jakob Disease (vCJD).
As surgical techniques advance, the realm of medical devices are transforming into increasingly sophisticated technologies, many of which involve robotic and AI systems. Is the science of Decontamination keeping pace? Should our Health Technical Memorandums be more pro-active and easier to review and change?
Government directives, related to sustainability and the transition to net zero, provides difficulties to Decontamination providers. We are being urged to evaluate our systems and consider whether our decontamination practises can be more environmentally friendly? Does such change return us to bygone days with acknowledged risks?
Historically medical device decontamination has been based upon the criteria listed within the Spaulding classification for microbial reduction. This guidance evolved around the Second world war and is this still relevant?
As Henry Ford stated, ‘If we always do what we always done, we always get, what we always got’. Is it time for revolution or evolution?
Presentation - Lean Trays (Confirmed)
Lean Trays
Myself and the Lean Trays Project Manager Steven Chawk will be presenting our work on Lean Trays within the National Green Theatre Programme at the Centre for Sustainable Delivery. We will present the rationale for lean surgical trays and our progress on the Scotland wide project.
Presentation - Evaluation of the performance of test soils used to validate washer disinfector (Confirmed)
Evaluation of the performance of test soils used to validate washer disinfector
Synopsis TBC
Q&A
Q&A
Closing Remarks
Closing Remarks
End of Day
End of Day