- Autokoriteollisuus ry
- Kaapeliteollisuusyhdistys ry
- Kaivannaisteollisuus ry
- LVI-talotekniikkateollisuus ry
- Meriteollisuus ry
- Metallinjalostajat ry
- Metalliteollisuudenharjoittajain Liitto - MTHL:n Työnantajat
- Suomen Polkupyöräteollisuusyhdistys ry
- Suomen Puolustus- ja Ilmailuteollisuusyhdistys PIA ry
- Suunnittelu- ja konsulttitoimistojen liitto Skol ry
- Terveysteknologian Liitto ry
- Valutuoteteollisuusyhdistys ry
- Kilpailulainsäädäntö
- Toimialayhdistykset-etusivu
RISK MANAGEMENT FOR MEDICAL DEVICE SOFTWARE
- BETTER COMPLIANCE AND FASTER RESULTS
Date: 6th-7th of September 2010
Location: Technopolis Helsinki-Vantaa,
Teknobulevardi 3-5, 01530 VANTAA
Price: 1150 / 960* Euro (*FiHTA/FFTI members)
IEC/ISO-62304, ISO-14971, IEC-80002 and the revised Medical Device Directive
The Medical Device Directive has emphasized the need for having an integrated SW Risk Management process when developing Medical Devices.
“For devices which incorporate software or which are medical software in themselves, the software must be validated according to the state of the art taking into account the principles of development lifecycle, risk management, validation and verification.”
The course will be held by Robert Ginsberg, who was one of the co-authors of IEC/ISO-62304.
For more information:
*) Course fee (2 days):
1150 euros/participant. For FiHTA and Teknologiateollisuus (FFTI) member companies 960 euros/participant. VAT 23% shall be added to the fee. If there is three or more participants/company reduction of 50 euros/participant shall be granted. The fee includes: lectures, course materials, coffee and lunch on both days.
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