New York Professional Events List


Applying ISO14971 / IEC62304 / IEC62366-1 A Practical Guide On How To Implement Risk Management


Date
May 18, 2017 - 09:00 AM - May 19, 06:00 PM
Organizer
GlobalCompliancePanel
Location
Hilton Zurich Airport Zurich, Switzerland,

Zurich,
Switzerland,
US,
ZIP: Switzerland
Phone: +1 929.900.1853

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.


Who Will Benefit:

  • 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
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Please contact the event manager Marilyn below for the following:
- For Registrations Please call +1 929.900.1853
- Discounts for registering 5 or more participants.
- If you company requires a price quotation.
Event Manager Contact: marilyn.b.turner(at)nyeventslist.com
You can also contact us if you require a visa invitation letter, after ticket purchase.
We can also provide a certificate of completion for this event if required.
 
NO REFUNDS OR TRANSFER ALLOWED ON REGISTRATIONS
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Agenda


Day 1 Schedule

Lecture 1:

Introduction To Risk Management And Quality System Integration

  • Why Perform Risk Management?
  • Historical Perspective
  • International Regulatory / Statutory Requirements
  • Risk Management Lifecycle And Stakeholders
  • Over-Reaching Concept
  • Integration Into ISO13485
  • Lifecycle Steps
  • Risk Management Benefits
  • Liability Issues
  • Streamlining Product Development
  • Improving Product Safety And Quality
  • How To Implement Risk Management Into ISO13485
  • SOP Framework
    • Planning And Execution
    • Monitoring And Control

Lecture 2:

Risk Management To ISO 14971:2012

  • Risk Management Planning
  • Risk Management Life Cycle
  • Hazard Identification
    • Hazard Domains
    • Hazard Latency Issues
  • Risk Rating Methods
  • Initial (Unmitigated) Risk Assessment
  • Mitigation Strategies And Priorities
  • Mitigation Architectures
  • Alarm Systems As Mitigations
  • Risk Control Bundles
  • Post Mitigation Risk
  • Residual Risk
  • Risk-Benefit Analysis
  • Safety Integrity Levels
  • European Special Requirements (Z-Annexes)
  • Safety Requirements
  • Hazard Mitigation Traceability
  • Verification Planning
  • Architectures, Redundancy, And Diversity
  • Failure Rates / Modes / Types
  • Failure Mode And Effect Analysis
  • Tips And Tricks
  • Q&A

Day 2 Schedule


Lecture 1:

Software And Usability In Risk Management

Software Risk Management (IEC62304 / FDA Software Reviewers' Guidance)
  • Critical Software Issues
  • Software Hazard Mitigation Strategies
  • Software Item, Unit, And System Definition
  • Software Failures As Hazard Sources
  • Software Requirements And Design
  • Software Specification
  • Tools And Development Environment
  • Software Unit And Integration Verification / Testing
  • Real-Time System Challenges
  • Software Verification And Validation
  • Mitigation Traceability And Effectiveness
  • Software Maintenance And Configuration Control
  • Software Risk Management Process - Integration Into ISO14971
  • Legacy Software Issues
  • FDA Documentation Requirements
  • Tips And Tricks
Usability And Risk Management (IEC62366-1/-2 / FDA Human Factors Guidance)
  • Use Errors As Hazard Source
  • User Intervention As Hazard Mitigation
  • Usability Engineering Lifecycle
  • Usability Evaluation Methods
  • Usability Specification
  • User Interface Specification
  • Formative Testing / Summative Evaluation
  • Usability Verification / Validation
  • The New Issues In IEC62366-1:2015

Lecture 2:

Risk Management Report And Safety Case

  • Safety / Assurance Case
  • Safety Classification
  • Basic Safety / Environment
  • Documentation Of Basic Safety
    • Electrical Safety
    • Mechanical Safety
    • EMC / RFI Safety
    • Safety Margins
  • Documentation Of Essential Performance
  • What Is Essential Performance?
  • Device Architectures And Mitigation Allocation
  • Device Specific Mitigations
  • Software Mitigations
  • External Safety
  • User Intervention And Alarms
  • Organizational Measures
  • Levels Of Protection Concept
  • Verification Of Safety Properties
    • Type Testing / Sample Testing
    • Verification Testing
    • Inspections
    • Analyses
  • Assurance Case Vs. Risk Management Report
  • General Safety And Hazard Avoidance
  • Device / Application Specific Issues
  • Tips And Tricks
  • Q&A


Speaker Details


Markus Weber

Principal Consultant, System Safety Inc.
 

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.


Event Categories
BUSINESS & MANAGEMENT CONFERENCES
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EDUCATION CONFERENCES
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Technology
Keywords: fun, design , development , environment, Fun , hardware, implement, Management , professional, purchas




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