The core activity of CARAG AG is the development of medical products, in particular implants, as well as the provision of engineering and consulting services for the medical technology industry. This includes, among other things, the development of prototypes, the conduct of tests and measurements, the creation of approval documents and support for the market approval of medical products.
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Industry:Medical Technology Industry
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Engineering and consulting services for physicians and Medtech companies; development of new medical devices from idea to market readiness, including technical and personnel resources.
Engineering
Development of Medtech solutions when engineering capacity is constrained; support with new concepts, solution approaches and technical implementation.
Electronics and software development
Development of electronic devices, firmware, software and apps using established processes to accelerate Medtech projects.
Prototyping
Rapid creation of prototypes for medical devices, with quality as close as possible to the end product.
Testing
Precise tests and measurements for medical technology products, including use of the company’s own infrastructure.
Implant development
Development of implants quickly and cost-effectively while maintaining safety and regulatory requirements.
Regulatory clearance and marketing approval
Support with certification, approval procedures and market-related authorisation of new medical devices up to market approval.
Clinical studies
Conducting and supporting clinical and in vivo studies as part of medical device development.
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