Consulting and Supporting for CE-/FDA-approval in the medical technology area
Accompanying the development is the generation of all documentation pertaining to CE or FDA guidelines.
We use our core competency to develop medical devices quickly
Aligning our development services with the standards of the FDA enables us to deliver our clients with a fast and effective certification within a short amount of time.
For BYTEC documentation means: from the very beginning the development process is conceived, supported & accelerated intelligently and safely.
We would be glad to support you in questions regarding cerfication.