We contributed to software validation and system integration in projects with high documentation and compliance requirements. We have extensive experience with CE- and ISO-related quality assurance, including testing, traceability, and documentation structures tailored to medical environments.
Our approach is based on close collaboration with QA and regulatory teams, ensuring high documentation quality and audit readiness. We manage the entire process from URS to final testing with deep domain understanding.
Collaboration with CLEVR
A collaboration usually starts with these three steps:
1
Qualification of the cooperation and the task
Together we qualify whether CLEVR Engineering is the right partner for the client and the content of the assignment is described.
2
Choice of consultant
CLEVR Engineering offers one or more qualified consultants.
3
Contracting
The start-up and duration of the assignment and the hourly rate are agreed and relevant agreements are signed; NDA, contracts, etc.
We ensure the right match between client and consultant. We take the time for the thoroughness needed for all parties to feel comfortable throughout the process, and of course we don’t charge for our time until we have a signed agreement and the consultant has started working with the client.
