FDA, UKCA, MDSAP

In the FDA-UKCA-MDSAP registration processes, we prepare the technical documentation in the light of the data obtained through the verification and documentation of the design and product realization, the design of the tests for pre-clinical and performance criteria. If you have processes that need attention and improvement at any stage, we offer development and evaluation activity, ensuring that the product and production become the best. We manage the application processes and provide communication between the institution and the competent authority. We run your process as a partner and serve as a part of you on your behalf.