Seminar on Medical Device Software Development at SFO, CA

Overview:

This seminar is mainly based on the IEC62304:2006 standard and will introduce the main elements and requirements for the development of modern software systems for medical devices. Emphasis is placed on understanding the underlying principles that generate the requirements of the standard, to understand strengths, the shortcomings and weak parts of the standard and give practical, proven guidance on how to implement the requirements necessary for regulatory approval. This seminar goes beyond teaching the mere content of the standard, but will provide the toolset to understand the underlying engineering principles that allow a justifiable interpretation of potential ambiguities of regulatory requirements. Understanding the basic principles of risk management, the failure modes of software, the architectural approaches available to mitigate software failures and the understanding of test methodologies are vital components to understand the 'spirit' of the requirements.

Software risk management has to be embedded into the bigger scope of overall risk management. Therefore, this course will additionally link to the system level risk management and the resulting interfaces to software. Risk probability and the impact on software based risk reduction will be discussed.

Who will benefit:

This course is developed to provide valuable assistance to all regulated companies that need to understand their software development processes including companies:

• Senior Quality Managers
• Quality Professionals
• Regulatory Professionals
• Compliance professionals
• Project Managers
• Software Project Managers
• Design Engineers
• Software Engineers
• Process Owners
• Quality Engineers
• Quality Auditors

Speaker:

Markus Weber is the owner and Principal Consultant with System Safety, Inc. He specializes in safety engineering and risk management for critical medical devices. With his background in embedded systems engineering (MSEE) Mr. Weber provides safety and regulatory compliance consulting to multiple industries for more than 20 years. Before founding his consulting company, 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. He teaches webinars, seminars and university courses on a regular basis.

Location: SFO, CA        Date: August 6th & 7th, 2015        Time: 9 AM to 6 PM 
Venue: DoubleTree by Hilton Hotel San Francisco Airport

Venue Address: 835 Airport Blvd., Burlingame CA 94010-9949

Price: $1,645.00 (Seminar for One Delegate)

Register now and save $200. (Early Bird)

Until June 30, Early Bird Price: $1,645.00

From July 01 to August 04, Regular Price: $1,845.00

Contact Information:

NetZealous LLC,

DBA GlobalCompliancePanel

161 Mission Falls Lane,

Suite 216, Fremont, CA 94539, USA         

USA Phone: 800-447-9407

Fax: 302-288-6884

support@globalcompliancepanel.com          

http://www.globalcompliancepanel.com

Event Registration Link - http://bit.ly/1EfIMDP