Conference Details

Medical Device Software Risk Management Standard | Software Expert 2018

Date :

Place : United States, San diego, ca

Website :

Contact Person:Event Manager

Description:

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

Medical Device Software Risk Management Standard | Software Expert 2018 will be held in San diego, ca,United States on date 2018-01-19

Deadline for abstracts/proposals : 16th January 2018

Organized By :NetZealous DBA as GlobalCompliancePanel

Keynote Speakers : 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 manufactu

Conference Highlights :Project managers Regulatory specialists Quality assurance specialists Documentation specialists Test managers Software team leaders and lead developers

Venue :San Diego, CA, United States

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Medical Device Software Risk Management Standard | Software Expert 2018

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