At your Side: Our Consulting Advice for Your Project
We advise you fully in all matters relating to your medical device - regulatory, technical and economical - during all stages of the product life cycle. Your team for legal service, EC-Rep and QM consulting: Our subsidiary bytec Legal Manufacturer GmbH.
BYTEC Medizintechnik GmbH
Eschweiler,
Germany
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BYTEC Consulting
At the beginning we conduct a classic feasibility study: Is your project feasible and at what cost? What market opportunities does your idea have and what are the risks? We advise you in an unbiased manner, including in cases where you need a second opinion to an already running project.
- Do you want to bring a new medical device onto the market?
- Do you want your product to be approved from MDD to MDR?
- Do you need advice on quality management?
