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Device Design and Risk Management
Medical device design is linked inextricably with risk management. Risk reduction measures become design inputs. Implementation verification, a risk management activity, can work as design verification too.
Governing it all is an alphabet-soup of Quality Management Systems (QMS) provisions including ISO 13485:2003, EN ISO 13485:2012, ISO 13485:2016, and EN ISO 13485:2016, as well as risk management requirements in the common Risk Management Systems (RMS): ISO 14971:2007 and EN ISO 14971:2012.
Order this session with a leading authority on in quality, operations, and program management in medical device design and manufacture.
Dan O’Leary of Ombu Enterprises has a long track record training operations management professionals via a unique systems approach perfected over 30 years of training. In 90 fast-paced minutes, he’ll cover a lot of ground:
Bonus! A chart showing relationships between the clauses of EN ISO 13485:2012 and EN ISO 14971:2012.
Better design and smoother operations benefit everyone — your employer, your customers, maybe your paycheck too. It’s well worth 90 minutes out of your week to sharpen skills and increase professional standing. Order now.
Dan O’Leary is President of Ombu Enterprises LLC, a consultancy offering training and execution in Operational Excellence. Based on more than 30 years of experience in quality, operations, and program management in regulated industries including aviation, defense, medical devices, and clinical labs, Mr. O’Leary has developed a unique systems approach to operations management that has benefited thousands of devicemakers. He is an ASQ-certified Biomedical Auditor, Quality Auditor, Quality Engineer and Reliability Engineer and holds the Six Sigma Black Belt. He is APICS-certified in Resource Management.
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