QNX Info Day: Challenges Of Commercializing Regulated Medical Devices

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

Keynote Speaker

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:
Patryk Fournier
QNX Software Systems

Serious Enquiries Only, Please


Register Here