New York Professional Events List


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


Date
May 22, 2017 - 09:00 AM - May 23, 06:00 PM
Organizer
GlobalCompliancePanel
Venue
Singapore
Location
Singapore,

Singapore,
Singapore,
US,
ZIP: Singapore
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
===
Please contact the event manager Marilyn below for the following:
- Discounts for registering 5 or more participants.
- If you company requires a price quotation.
- For event ticket, contact +1 929 900 1853
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
,
Technology
Keywords: fun, design , development , environment, Fun , hardware, implement, Management , professional, purchas




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