A guide to practical Risk Management - Applying ISO14971 and IEC62304

Website http://www.globalcompliancepanel.com/seminar/applying-ISO-practical-risk-management-901963SEMINAR?ou | Edit Freely

Category Healthcare, technology, pharmaceuticals,medical courses, online trainings, 2019 trainings

Deadline: October 02, 2019 | Date: October 03, 2019-October 04, 2019

Venue/Country: Philadelphia, PA, U.S.A

Updated: 2019-05-14 14:50:50 (GMT+9)

Call For Papers - CFP

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:

The course will introduce the main elements of risk management with emphasis on the application of risk management principles and requirements to the medical device development cycle. Risk management has become the method of choice to ensure an effective and safety oriented device development. International consensus, reflected in globally applicable standard requirements, has led to risk management being a mandatory component of almost any activity in the medical device industry.

• Quality professionals

• Regulatory professionals

• Compliance professionals

• Project managers

• Design engineers

• Software engineers

• Process owners

• Quality engineers

• Quality auditors

• Medical affairs

• Legal Professionals

Agenda:

Day 1 Schedule

Lecture 1:

Introduction into Risk Management and Quality System Integration

• Why 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

• Safety Integrity Levels

• European special requirements (Z-Annexes)

• Safety Requirements

• Hazard Mitigation Traceability

• Verification Planning

• Architectures, Redundancy and Diversity

• Failure Mode and Effect Analysis

• Tips and Tricks

• Q&A

Day 2 Schedule

Lecture 1:

Usability and Risk Management

• Use errors as hazard source

• User intervention as hazard mitigation

• Usability engineering lifecycle

• Application specification

• Usability Specification

• Frequently used functions / primary operating functions

• Usability verification / validation

• Upcoming changes IEC62366:2014

Lecture 2:

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 Specification

• Software Tools and Development Environment

Lecture 3:

Software Risk Management (IEC62304 / FDA software reviewers' guidance):

• Software Unit and Integration 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

• Upcoming changes in IEC62304:2014

• Tips and Tricks

Lecture 4:

Safety / Assurance case

• Safety classes

• Basic Safety / Environment

• Essential performance

• 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

• Software 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:

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.

Location: Philadelphia, PA Date: October 3rd and 4th, 2019 and Time 9:00 AM to 6:00 PM

Venue: WILL BE ANNOUNCED SOON

Price:

1 ATTENDEE $2,000, Regular Price: $2000, Register for 1 attendee

5 ATTENDEES $10,000, Regular Price: $10,000, Register for 5 attendees

10 ATTENDEES $20,000, Regular Price: $20,000, Register for 10 attendees

Until August 20, Early Bird Price: $2,000. From August 21 to October 01, Regular Price: $2,200.

Use this promo code GCP50 to get 50% off.

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