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Oxford Medical CE Marking Forum Seminar Series - April 2017
Mon 24 April 2017, 09:00 – 10:00 BST
Medical Device Risk Management – a holistic approach
Gurge Phull, Ph.D., Medical Regulatory Affairs Manager at Element. Element has laboratories worldwide and testing provide services to the Aircraft, Oil, Railway, Automotive, MOD and Medical industry. His team provides advice and resources to companies for worldwide medical device regulatory compliance.
over twenty years experience in the pharmaceutical industry (covering R&D, clinical and registrations)
worked with IVD’s (HIV, Hep C, etc), pathology instrumentation and training (customer/sales /service) for more than a decade
has more than 17 years experience working with medical devices
As main lead / head of quality assurance / regulatory affairs in the UK and abroad has experience and expertise:
in product design & development (inception to market launch), manufacturing, training,
auditing quality / regulatory systems for worldwide compliance (EU, USA, ROW – CE marking (MDD), FDA’s QSR, ISO 13485 etc)
standards and testing compliance
What are my parking options getting to the event?
There are paid parking bays within the Nuffield Orthopedic Centre near the BOTNAR Research Center.
Are there limits on the number of attendants?
Yes, there is a limit of 60 registrations on the first in first served basis.
How can I contact the organizer with any questions?