Risk Management for Medical Device SW
Sep 28, 2010
Webinar
Don’t miss this opportunity to take part in Synergus webinar on Risk Management for Medical Device SW!
The harmonization of standard IEC/ISO 62304 sets a new expectation level of what Medical Device manufacturer need to do regarding software validation.
A fundamental regulatory requirement related to Medical Device SW is conducting and following up the SW Risk Management analysis. Software is different compared to electronics and mechanics, and needs to be treated according to that fact.
Many vendors are implementing processes for SW validation, and are striving to find an optimal approach delivering safe products as a productive organization. When correctly implemented, SW Risk Management can optimize the amount of documentation needed and enable an effective Verification and Validation strategy.
Synergus Senior Consultant Robert Ginsberg will guide you through this topic in a 45 minutes webinar followed by 15 minutes of Q&A.
Time and Date
Tuesday September 28, 2010
The seminar will start at 15.00 CEST
Registration
The seminar is free of charge, please send an email to info@synergus.com or contact us at +46 8 544 767 58 to register.
Don’t hesitate to contact us if you have any questions.
Kind regards,
The Synergus Team