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Development of Medical Device Software according to IEC 62304

Software Development and Development Support by our Software Specialists.

PROSYSTEM supports your activities for the implementation of a software-lifecycle-process according to IEC 62304 to comply with regulatory documentation requirements. Our software specialists assist you during the software development and the compilation of the technical documentation including the software risk management- and the usability-file for medical software.

Our test engineers validate your medical device- and process software onsite or in our test lab according state of the art requirements. As a matter of course PROSYSTEM takes over the entire software development according to your specifications.

Contact us for further information or a non-binding quotation.

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