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Risk Management

May 2 @ 8:00 am - May 3 @ 5:00 pm

€699

Introduction to our two day Risk Management Training

The requirements for Product Risk Management as it pertains to all stages of a Medical Device Lifecycle is outlined in ISO 14971. The emphasis on the Risk Management process extends from Conformity and Compliance Assessments to assurances that Outsourced Processes, including Suppliers are thoroughly, adequately and appropriately audited with a Risk-based approach.

Who should Attend:
All personnel involved in areas relating to Quality, Production, Engineering, Supplier and Outsourced Process Management should be conversant with these requirements to provide assurance of Competency in Medical Device Product Risk Management.

This intensive course will focus on the requirements of the ISO 14971 and will demonstrate Risk Management practices that reflect best in class practices.

 

Tickets

12 available
ISO 14971 Risk Management 699Risk Management for Medical Device Industry

Details

Start:
May 2 @ 8:00 am
End:
May 3 @ 5:00 pm
Cost:
€699
Courses Categories:
,

Organiser

Philip Byrne

Venue

Dublin
Maldon Hotel Newlands Cross, Naas Road, Newlands Cross
Dublin 22, Co. Dublin D22 V6Y6 Ireland
+ Google Map
Phone:
+35314640140
Website:
https://www.maldronhotelnewlandscross.com/