Seminar: Software as a Medical Device:
Safety and security.
January 5, 9-11 am
Seminar room: Merkuur
Connected Health cluster presents a practical seminar to help health IT developers and startups plan and manage smoothly their products to comply with needed standards and rules.
9:00 What is a software as a medical device and what is required to get regulatory compliant products on the market - overview of medical device software safety, regulations in EU and US, standards and FDA guidance - Dr. Marion Lepmets, Co-Founder & CEO of SoftComply – 30 min presentation + 15 min Q&A
9:45 Privacy Engineering and Health Data: IT and IoT - Dr. Ian Oliver, Security Specialist at Bell Labs – 30 min presentation + 15 min Q&A
10:30 Discussion and 1-2-1 Q&A
Please register by January 3 the latest: services@tehnopol.ee
Free for Science Park Tehnopol network and service clients and Connected Health cluster members. 30€ + vat for others.
1 comment:
Software development for medical devices requaiers to comply with needed standards such as ISO 13485 and ISO 14971 and other regulations. You can find more information on pro4people - medical device software development
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