Seminar 2014 - 2-day In-person Seminar on “Applying ISO14971:2012 and IEC62304 - A Guide to Practical Risk Management” in London UK

Summary of the Workshop:
Gaps, 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 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.
To comprehensively summarize all risk related activities and to demonstrate the safe properties of a device the 'Safety Case' or 'Assurance Case' document is a well-established method to collect all safety related information together in one place. This documentation will most likely become mandatory for all devices (currently only required for FDA infusion pump submissions). This course will introduce the basic concepts and content of safety assurance cases and will illustrate the usefulness for internal and external review of safety related information.
Learning Objectives:
Introduction into Risk Management and Quality System Integration
Risk Management to ISO 14971:2012
Usability and Risk Management
Software Risk Management (IEC62304 / FDA software reviewers' guidance)
Software Risk Management (IEC62304 / FDA software reviewers' guidance)
Safety / Assurance case
Meet your Expert:
Markus Weber is owner and Principal Consultant with System Safety, Inc. He 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 his consulting company, 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. Over the last 25 years Mr. Weber has helped hundreds of companies, from start-ups to Fortune 500 firms, to design safe medical devices. He trained hundreds of professionals on four continents in practical risk management and system safety methodologies. He frequently conducts webinars, in-person seminars, corporate training and he teaches Medical Device Risk Management the University of California Irvine Extension.
RAC Credits: 12
Date: October 27th & 28th, 2014
Event Details: http://bit.ly/AGuidetoPracticalRiskManagement
Location: London, UK
Venue: Will Be Announced Soon
Registration: Open Enrollment
Delivery: Face-to-Face event
Price: $1595.00
Until September 15, Early Bird Price: $1,595.00
From September 16 to October 21, Regular Price: $1,795.00
Audience: Senior quality managers, Quality professionals, Regulatory professionals, Compliance professionals, Project managers, Design engineers, Software engineers, Process owners, Quality engineers, Quality auditors, Medical affairs, Legal Professionals.
Course Web Site: https://www.globalcompliancepanel.com/control/~pro...
Organizer:
GlobalCompliancePanel imparts knowledge of best practices in industry to guarantee effective implementation of compliance programs for meeting regulatory demands. The key focus of GlobalCompliancePanel is to provide extensive and quality training for risk management, regulatory compliances, corporate governance and quality management.
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Provider:
GlobalCompliancePanel
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