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Development of an automated sample transfer module

Project duration: 5 months

Brief description

Consulting and development support for an automated sample transfer module in line with regulatory requirements.

Supplement

The connection module for sample transfer has already completed its development on the hardware side. The software is currently under development at a third-party company. In order for a medical technology device to be certified, the development process must be documented and also the system must be verified and validated according to the required quality directives. The documents for the internal quality management handbook as well as the test strategies must be drawn up and optimized.

Subject description

In order for a project to be successful in the medical technology environment, it is necessary for clear and testable requirements to be imposed on all system levels for the HW/SW developer. The structure and levels of the requirements must be described in an overarching quality management plan. This describes the traceability between the requirements through to the test regulations.

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Ole Knudsen

Key Account Manager

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