Gaps and/or incorrect or incomplete implementation of safety functionality can delay or make the certification/approval of medical products impossible. Most activities cannot be retroactively performed since they are closely linked into the development lifecycle. Diligent, complete and correct implementation of risk management from the start of product development is therefore imperative. This course will introduce all the steps necessary 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 : 20th July 2017 to 21st July 2017

Place : United States, Courtyard arlington crystal city/reagan national airport

Website :http://www.globalcompliancepanel.com/control/globalseminars/~product_id=901006SEMINAR?allconferencealerts_july_2017_SEO

Contact Person:Eevnt Manager

Description:

Gaps and/or incorrect or incomplete implementation of safety functionality can delay or make the certification/approval of medical products impossible. Most activities cannot be retroactively performed since they are closely linked into the development lifecycle. Diligent, complete and correct implementation of risk management from the start of product development is therefore imperative. This course will introduce all the steps necessary 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.

Gaps and/or incorrect or incomplete implementation of safety functionality can delay or make the certification/approval of medical products impossible. Most activities cannot be retroactively performed since they are closely linked into the development lifecycle. Diligent, complete and correct implementation of risk management from the start of product development is therefore imperative. This course will introduce all the steps necessary 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 Courtyard arlington crystal city/reagan national airport,United States on date 2017-07-21

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Deadline for abstracts/proposals : 18th July 2017

Keynote Speakers : Markus Weber, Principal Consultant with System Safety, Inc., specializes in safety engineering and risk management for critical medical devices. He graduated from Ruhr University in Bochum, Germany with a MS in Electrical Engineering. Before founding System Safety, Inc., he was a software safety engineer for the German approval agency, TUV. Since 1991, Mr. Weber has been a leading consultant to the medical device industry on safety and regulatory compliance issues, specifically for active and so

Conference Highlights :Senior Quality Managers Quality Professionals Regulatory Professionals Compliance Professionals Project Managers Design Engineers Software Engineers Hardware / Embedded System Engineers Process Owners Quality Engineers Quality Auditors Medical Affairs Professionals

Venue :Washington, D.C., DC, United States

Check the event website for more details.