EIR Brochure Final 2 Paperturn - Flipbook - Page 13
RICHARD HALL
QA
QMS Technology
BEN WENSLEY-STOCK
Managing Director
MPS-UK & Wensley Stock LTD
STEVEN HAKEN
Director
Odelle Technology
DEBORAH RIZZI
Director
Odelle Technology
Richard is an experienced QA
professional, having worked within
the medical device industry since
1993. With experience of
developing and manufacturing
medical devices in a range of
companies, from start-up to blue
chip international healthcare
businesses, Richard has a strong
understanding of new product
development; he has been named on
two patents and lectures at Imperial
College London regarding
Regulations and CE Marking.
Ben Wensley-Stock has over 20
years’ experience in HealthTech and
MedTech industries working in CxO
positions within both established
multinational and start-up
companies. Ben now tends to
specialise in network connected
medical devices that involve
software or that employ deeplearning or machine-learning
technologies. Ben has successfully
helped over 30 medical device
companies of varying sizes across
the globe to bring innovative
products to market.
A Director of Odelle Technology
based in the UK and France,
Steven specialises in Market
Access, reimbursement, and
Government Affairs for
MedTech’s. Steven previously coinvented and commercialised 28
Medical technologies across the
EU and USA. PhD in Mathematics
and further education in
Physiology and information
technology. Clinical experience in
ICU, CCU, Operating theatres,
Neurology and Emergency
Medicine.
Deborah started her medical career
as a Registered Nurse in Australia.
Throughout her ten years in this
position, she worked in numerous
areas in both medical and surgical
fields. In 2006, she transitioned into
Industry, working with both smaller
businesses and Blue-Chip companies.
This experience allowed her to gain a
unique insight into the industry by
exposing her to all sides of the
medical device spectrum. Deborah
has extensive experience in bringing
new products to markets and helping
clients secure the successful
distribution of their technology.
Richard can advise on:
Medical Device Regulations,
MDR, IVDR, UKMDR, FDA,
WHO, MDSAP, India.
Product Classification, MD,
IVD, SaMD.
Quality Management Systems,
QMS & ISO 13485.
Ben can advise on:
Device classification and
regulatory planning.
Product realisation planning.
International medical device,
security and privacy
regulations.
Research and
design/development
strategies.
Steven can advise on:
Market Access and
Reimbursement in the UK
and EU.
Routes to progress across
the EU.
Career development for
early career researchers.
Deborah can advise on:
Market Access and
Reimbursement in the UK and
EU.
Routes to progress across the
EU.
Career development for early
career researchers.