Overview: IEC4 is a internationally recognized 2012 - IEC 62304 for Medical Device Software Development: Steps to Compliance - Webinar By GlobalCompliancePanel
Date2012-07-19
Deadline2012-07-19
VenueWilmington, USA - United States
KeywordsIEC 62304,Medical Device Software Development, software lifecycle standard,requirements specification, integration testing, real-time systems
Websitehttp://alturl.com/oterg
Topics/Call fo Papers
Questions like:
How much detail is required in the requirement specification?
What is a software unit?
How can integration testing be performed without test harnesses?
will be answered. Practical guidance on how to employ a streamlined but yet compliant development process will be given.
Why should you attend: This webinar will explain basic design control concepts and the criticality dependent requirements for software development. Software specification, architectures and resulting design documentation will be discussed, as well as practical tips on how to streamline the development process and minimize the regulatory burden.
Areas Covered in the Session:
Software requirements specification
How to write meaningful requirements
Software architectures
Multi software system implementation
Software design documentation
Requirements traceability
Software unit and integration testing
Software testing in real-time systems
Software tools
SOUP (software of unknown providence)
Who Will Benefit:
Project Management
Regulatory / Quality Control
Software Engineering
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 software-controlled devices. In conjunction with the FDA, he has published works on risk management issues and software-related risk mitigations. Mr. Weber has helped multiple companies, from startups to Fortune 500 firms.
Price List:
Live : $245.00
Corporate live : $495.00
Recorded : $295.00
Phone: 800-447-9407
Fax: 302-288-6884
webinars-AT-globalcompliancepanel.com
http://www.globalcompliancepanel.com
How much detail is required in the requirement specification?
What is a software unit?
How can integration testing be performed without test harnesses?
will be answered. Practical guidance on how to employ a streamlined but yet compliant development process will be given.
Why should you attend: This webinar will explain basic design control concepts and the criticality dependent requirements for software development. Software specification, architectures and resulting design documentation will be discussed, as well as practical tips on how to streamline the development process and minimize the regulatory burden.
Areas Covered in the Session:
Software requirements specification
How to write meaningful requirements
Software architectures
Multi software system implementation
Software design documentation
Requirements traceability
Software unit and integration testing
Software testing in real-time systems
Software tools
SOUP (software of unknown providence)
Who Will Benefit:
Project Management
Regulatory / Quality Control
Software Engineering
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 software-controlled devices. In conjunction with the FDA, he has published works on risk management issues and software-related risk mitigations. Mr. Weber has helped multiple companies, from startups to Fortune 500 firms.
Price List:
Live : $245.00
Corporate live : $495.00
Recorded : $295.00
Phone: 800-447-9407
Fax: 302-288-6884
webinars-AT-globalcompliancepanel.com
http://www.globalcompliancepanel.com
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Last modified: 2012-06-28 13:21:45