This course will introduce all necessary steps to design, implement and test critical medical devices in a regulatory compliant environment. This course will additionally address the software risk management and the resulting interfaces to device level risk management.

Date : 18th May 2017 to 19th May 2017

Place : Switzerland, Opfikon

Website :http://www.globalcompliancepanel.com/control/globalseminars/~product_id=900892SEMINAR?channel=mailer&camp=seminar&AdGroup=allconferencealerts_May_2017_SEO

Contact Person:Event Manager

Description:

This course will introduce all necessary steps to design, implement and test critical medical devices in a regulatory compliant environment. This course will additionally address the software risk management and the resulting interfaces to device level risk management.

This course will introduce all necessary steps to design, implement and test critical medical devices in a regulatory compliant environment. This course will additionally address the software risk management and the resulting interfaces to device level risk management. will be held in Opfikon,Switzerland on date 2017-05-19

---

Deadline for abstracts/proposals : 16th May 2017

Keynote Speakers :

Venue :Zürich, Switzerland

Check the event website for more details.