Software Design for Medical Devices Europe 2012
January 31 - February 2, 2012
Ensuring Compliance to Evolving Regulations and Standards whilst Incorporating Quality & Usability into Agile Design
Are you compliant with the upcoming 3rd edition of IEC 60601 in June? Are your processes Agile, and are those that are Agile really as Agile as they could be? Do you incorporate human factors into your software design? Are those processes compliant with the FDA’s new draft guidelines on usability in medical devices?
These are the sort of questions that the most clued-up software engineers and project leaders are asking themselves, which is why they are planning to attend Software Design for Medical Devices Europe 2012 (or SDMD 2012 for short) - the only pan-European and English-language conference that is dedicated to the important area of software design in the Medical Device industry.
Are you compliant with the upcoming 3rd edition of IEC 60601 in June? Are your processes Agile, and are those that are Agile really as Agile as they could be? Do you incorporate human factors into your software design? Are those processes compliant with the FDA’s new draft guidelines on usability in medical devices?
These are the sort of questions that the most clued-up software engineers and project leaders are asking themselves, which is why they are planning to attend Software Design for Medical Devices Europe 2012 (or SDMD 2012 for short) - the only pan-European and English-language conference that is dedicated to the important area of software design in the Medical Device industry.
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