Why attend this conference?
This is the final Medical Device Testing and Compliance Seminar for 2013. It offers a variety of sessions covering how to successfully test your medical devices, ensure compliance and access new markets against a range of different legislation, with additional one to one meetings to discuss how to prepare your own medical devices for testing and certification.
Reflecting on what is top on many Quality & Regulatory Managers' minds these days, this seminar will focus on current legislation and how this applies to UK companies looking to extend their horizon into Europe or the rest of the world. We will present strategies drawn from our extensive testing experience to help you understand how you can achieve compliance and reach these new markets.
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|09:00 - 09:30
|09:30 - 09:45
Mark Heaven - CEO, TRaC Global
|09:45 - 10:30
||Medical Device Overview/Update
Martin Penver - Operations and Technical Manager, LRQA
|10:30 - 11:00
||The Importance of Quality Management in Medical Devices
Gurge Phull - TRaC Global
|11:00 - 11:30
||Morning Coffee and Networking
|11:30 - 12:00
||Wireless Technology in Medical Devices
Dr Simon Hindle - Principal Radio Engineer, TRaC Global
|12:00 - 12:30
||A Case Study - Bringing your Medical Device to Market
John Chewins - BioxyQuell Product Manager, Bioquell
|12:30 - 13:30
|13:30 - 14:30
Interaction of Risk Management into EN 60601-1
Chris Rouse - Safety Director, TRaC Global
One-to-one Compliance Surgeries
About TRaC Global
TRaC Global is a leading testing and certification group for companies needing to achieve product compliance. Every year TRaC tests over 2,500 products and helps companies take their products to market. TRaC is a UKAS accredited test laboratory for EMC, Safety, Radio, Environmental and Telecoms as well as a National Certification Body and a Certified Body Test Laboratory for international products and approvals.
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