QNX is hosting an Info Day this upcoming May 19th in Cambridge - the hotbed of medical device activity in the UK.
The event is aimed at the education surrounding challenges presented to device manufacturers with producing medical device technology in today's public markets. Aiming to help companies that are taking their innovations from the concept stage, through regulatory approval and eventually to the market; the event will promote networking and addressing the associated software, regulatory and competitive issues.
Specific topics to be addressed include:
- IEC 62304 Compliance
- MHRA, FDA and European Commission regulations
- Streamlining software integration
- Ensuring medical device safety, mitigate project risk and ease the path to end device approval
Rob Higgins, Regulatory Affairs Section Head, Medicines and Healthcare products Regulatory Agency (MHRA)
Date: 19 May 2015
Time: 08:00 – Registration | 09:00 – Opening Remarks | 16:30 – End of Info Day
Venue: The Cambridge Belfry Back Lane, Cambourne, Cambridge, CB23 6BW United Kingdom
Registration: Complimentary Pass
Included: Catered Lunch, Networking Coffee Breaks
For more information, please contact:
QNX Software Systems
Serious Enquiries Only, Please