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Medical Device Software: An Incremental Approach to Risk and Quality Management

Du Lundi 11 Juin 2018 au Jeudi 12 Juin 2081 à CA
A partir de: 09:00
Secteurs concernés: Informatique médical -
DESCRIPTION
Course "Medical Device Software: An Incremental Approach to Risk and Quality Management" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion.

Overview:
Engineers are dedicated to making things work, so a focus on how they might fail and harm someone can seem alien.
Managing risk, however, is essential for all medical products- medical devices, including those involving software, have produced some painful examples of poor risk management with serious consequences. Experience has shown that there is a better way, that it is possible to manage risk in a changing business and technical world.
Regulatory bodies are placing increased emphasis on risk management, and technology shifts are introducing new sources of risk. Newer Lean-Agile methods are recognized by the FDA as a good way to accomplish risk management.
Techniques for risk management are well established, but require specific interpretation when applied to software. In this session, we will show a way of knitting risk management into the development process, so that it is integral to product development, not a ten ton caboose dragging the train back down the mountain.
Why you should attend:
Perhaps your engineering team is beginning its transition to an Agile approach - or perhaps you have a seasoned Agile team and you're just beginning work on FDA-regulated products. You know that risk management is required, but it's not at all clear how you should address it as you go through your backlog grooming, iterations, and end-user demonstrations. The process in ISO 14971 seems "linear" and unsuited to a highly iterative, dynamic lifecycle. How can you fit it into your approach?
Areas Covered in the Session:
• Software has introduced (or been blamed for) some serious safety hazards
• All medical device standards intersect on the topic of risk management
• Risk analysis starts with the intended use statement
• Risk information is available from multipl sources - use them!
• Note that safety is an emergent property
• Changes are often the biggest sources of risk
• Don't ignore the human factors side; understanding your users is crucial to safety
• Applying engineering risk methods to software requires us to translate some concepts
• Though standards draw a roadmap for risk management, WE must figure out the route
• Risks often arise when we add new features - so incremental risk management is the most effective
• Forget the notion that "software can't hurt anyone"
• Never conduct risk analysis by using a checklist from 14971
• Exploding technology brings numerous chances for risk to multiply
Who will benefit:
• Project managers
• Regulatory specialists
• Quality assurance specialists
• Documentation specialists
• Test managers
• Software team leaders and lead developers
Agenda:
Day 1 Schedule
________________________________________
Lecture 1:
Software brings great capability to medical devices, but also creates hazards
________________________________________
Lecture 2:
Consider how the key standards lay out the roadmap for managing risk
________________________________________
Lecture 3:
Understand the key concepts - hazard, risk, and harm
________________________________________
Lecture 4:
Walk through ISO 14971 in detail - and consider IEC 80002-1 for specific software concerns
Day 2 Schedule
________________________________________
Lecture 1:
Fault tree analysis and FMEA complement each other for risk analysis
________________________________________
Lecture 2:
Risk analysis for software is different from hardware - and needs a place in the lifecycle
________________________________________
Lecture 3:
Story mapping helps bring risk management directly into development
________________________________________
Lecture 4:
An incremental approach manages both risk and quality

Speaker:

Brian Shoemaker
Brian Shoemaker consults for healthcare products companies on computer system validation, software quality assurance, and electronic records and signatures. He has conducted validation both on product software and on internal software, developed software quality systems, audited software quality processes (including agile methodology), and evaluated 21 CFR Part 11 compliance. He has had clients in clinical diagnostics, medical device engineering, medical imaging, medical-device fabrics manufacturing, contract lyophilization, clinical trial software, dental prosthetics, and bone-repair implants. He has worked with companies in Germany and Switzerland as well as the U.S.
Previous to founding ShoeBar Associates, Brian had quality roles at PPD Informatics, Doxis, Inc., and Behring Diagnostics, Inc. Brian earned his Ph.D. in chemistry from the University of Illinois; he has achieved the ASQ Software Quality Engineer certification.

Location:  San Diego, CA Date: June 11th & 12th, 2018 and Time: 9:00 AM to 6:00 PM
Venue:  DoubleTree by Hilton San Diego Downtown 1646 Front St, San Diego, CA 92101, USA

Price:
Price: $1,495.00 (Seminar Fee for One Delegate)
Register for 5 attendees Price: $4,485.00 $7,475.00 You Save: $2,990.00 (40%)*
Register for 10 attendees Price: $8,222.00 $14,950.00 You Save: $6,728.00 (45%)*
Sponsorship Program benefits for “Biostatistics for Non-Statistician” seminar
For More Information- https://www.globalcompliancepanel.com/control/sponsorship 
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PUBLIC, SECTEURS, ACCREDITATION
Accréditations : 0
Public concerné: Professionnel
Audience: Internationnale
Visiteurs/Participants: 50
Conférenciers: 1
Exposants: 1
Type d'événement: Colloque
Secteur principal: INFORMATIQUE MEDICAL
Secteurs concernés: Informatique médical -
ORGANISATEUR / ANNONCEUR

NETZEALOUS LLC - GLOBALCOMPLIANCEPANEL
161 Mission Falls Lane, Suite 216
94539 Fremont
UNITED STATES

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REFERENCE
Congrès, formations ou conférences médicales REF #28-8045
Congrès, formations ou conférences médicales en INFORMATIQUE MEDICAL
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