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Evènement :Applying ISO14971 and IEC62304 | Risk Management Seminar 2018

Dates :Jeudi 14 Juin 2018 - Vendredi 15 Juin 2018

Lieu :Four Points by Sheraton Boston Logan Airport
407 Squire Rd
02151 Revere,MA, Massachusetts, États-Unis

Type :Conférence & Séminaire - Audience Internationale

Accréditation :--


 

Informations

Course "Applying ISO14971 and IEC62304 - A guide to practical Risk Management" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion.

 

Overview:

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.

The course will emphasize the implementation of risk management into the development and maintenance process. It will use real-life examples and proven tips and tricks to make the application of risk management a practical and beneficial undertaking. This seminar will address the system level issues of risk management as well as the increasingly important software and usability related issues of critical systems. It will help to comply with regulatory requirements with minimized overhead and resource burden. To make the combines effort to design, implement and verify a safe device transparent the concept of an assurance case will be introduced.

The course is mainly based on international consensus requirements such as ISO14971, IEC62366 and IEC62304. It will cover European (MDD), US (FDA) and international risk management requirements from a regulatory and practitioner's perspective.

Following personnel will benefit from the course:

  • 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

 

Agenda:

 

  • 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
  • Safety Integrity Levels
  • Residual Risk
  • 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
  • What is essential performance?
  • Device architectures and mitigation allocation
  • Device specific mitigations
  • Software mitigations
  • User intervention and alarms
  • Organizational measures
  • Levels of protection concept
  • Type testing
  • Sample testing
  • Software verification testing
  • Inspections
  • Analyses
  • General safety and hazard avoidance
  • Device / application specific issues
  • Documentation of essential performance
  • External safety
  • Verification of safety properties
  • Assurance case vs. Risk Management Report
  • 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:  Boston, MA  Date: June 14th & 15th, 2018 and Time: 9:00 AM to 6:00 PM

Venue:  Four Points by Sheraton Boston Logan Airport Revere, MA 407 Squire Rd, Revere, Massachusetts 02151, United States

 

Price:

Price: $1,295.00 (Seminar Fee for One Delegate)

 Register for 5 attendees Price: $3,885.00 $6,475.00 You Save: $2,590.00 (40%)*

 Register for 10 attendees Price: $7,122.00 $12,950.00 You Save: $5,828.00 (45%)*

 Register now and save $200. (Early Bird)

Until May 10, Early Bird Price: $1,295.00 From May 11 to June 12, Regular Price: $1,495.00

Sponsorship Program benefits for “Applying ISO14971 and IEC62304” seminar

For More Information- https://www.globalcompliancepanel.com/control/sponsorship

Contact us today!

NetZealous LLC DBA GlobalCompliancePanel

john.robinson@globalcompliancepanel.com  

Toll free: +1-800-447-9407

Phone: +1-510-584-9661

 Website: http://www.globalcompliancepanel.com

 

Registration Link - https://www.globalcompliancepanel.com/control/globalseminars/~product_id=901732SEMINAR?doctorama.com_june_2018_seo

 

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Lieu

Plan et itinéraire
Adresse de la conférence :
Four Points by Sheraton Boston Logan Airport
407 Squire Rd
02151 Revere,MA
Massachusetts, États-Unis
Tél : 8004479407
Plan et itinéraire

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Applying ISO14971 and IEC62304 | Risk Management Seminar 2018 Médecine - Pharmacie
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