Test phase in the Verification process

Resource shortage shortly before product launch

After two years of development work on a class IIa device with a new user interface, things suddenly had to move fast: The date for the product launch had been announced and there were only a few weeks left. However, internal resources for the decisive system test phase at the end of the project were not available in sufficient numbers due to redistribution within the business unit. So there was no more time to build up a new internal team and make it productive.

A qtec team of 5 colleagues and a project manager undertook the task. All team members were trained in the processes of creating test cases and the required devices in close cooperation with the customer. After the development of an appropriate test strategy, the actual Verification could be implemented

Due to the close cooperation between the client and the qtec team, all necessary work packages could be completed in time for the product launch.

Project Key Figures

Size of the client company
10.000 coworkers
qtec team size
5 Verification experts
Time between inquiry and project start
14 days
Total project duration
12 weeks

Our expert knowledge for your success

We have in-depth, worldwide expertise in the Approval and registration of Medical Devices. I will answer your questions about the MDR and put together a team for your project upon request.

Contact +49 451 808 503 60
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