We provide design solutions of implants and instruments on behalf of manufacturers with an iso 13485 and 21 cfr 820 approach.
We are fully interoperable with your system. Beyond pure design activities we are able to provide all deliverables in order to support your research and development activities.
- Imprint medical approach enables your project to follow a clear and reliable development path.
- Early visibility, concurrent engineering and upstream assessments of regulatory path are some of the means that allow a maximal efficiency during development
- In limiting uncertainties, step by step, you’re able to contain the incremental complexity and ill-timed costs of the project.
- This methodology allows to serenely limit the time to market your product, in insuring compliance of regulation requirements,
Patient safety, regulatory compliance, customer satisfaction