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Requirements Engineering

ASQF e.V.

The ASQF is the largest specialist network for software quality in German-speaking countries and an important partner for developers, decision-makers and companies in the IT industry. More than 1,100 globally active companies, high-performing small and medium-sized enterprises, institutions of higher education and research institutes, specialists and students are members of ASQF. They all share the commitment to quality standards in information and communication technology.

Pro F&E GmbH

Pro F&E GmbH provides consulting services for the optimisation of your product development processes (from design to production) and supports you and your development projects.

The name "Pro F&E GmbH" derives from "Prozesse für Forschung und Entwicklung" (processes for research and development). Our customers are companies marketing mechatronic products, i.e.

H-04: Data quality and innovative capability of medical products

The integration of medical products into the actual workflows and working processes of a productive environment is a difficult, time-consuming and cost-intensive task for both manufacturers and operators. Despite the standardization of DICOM and HL7, the integration of software components and medical products into a hospital information system still represents a huge task, owing to a lack of appropriate validation environments. The objective of this project is to create a generic test environment for medical products and a method of systematic generation of appropriate test data.

The

LA2 GmbH

We develop critical software based on web technologies for the health care industry and provide consulting services to software companies in a regulated environment.

LA2 GmbH has developed critical enterprise software - based on web technologies - for the health care industry since 1999. LA2 does not only assist its customers with the implementation, LA2 helps its customers with specification and requirements gathering, project management and problems in the regulated environment (e.g. workshops/advice/certification for FDA 21 CFR Part 11 and EU GMP Annex 11).

Contact

Marc Holfelder