The second publication by the DGBMT in the field of "Standards in Biomedical Engineering" deals with the development and production of medical software.
It is the first publication to cover all aspects of medical software development:
- legal requirements for medical software,
- medical software - from idea to product,
- the benefit of standards in software development and
- an outlook on future requirements.
All information is based on the new European regulations on medical devices and in-vitro diagnostics as well as the latest standards.
The publication is suitable for professionals as well as for beginners.
The publication is already available in German and will be published in English shortly.