Clinical studies and the data collected are used to prove whether a new medical device and/or procedure is actually suitable for the intended purpose or if the expected and desired results are achieved when it is used on patients.
As in all phases of the development and approval process, extensive formal requirements and specific procedures must be observed. We help you to plan, design and implement the necessary studies
and present the results of your study in a substantiated and binding manner.
You benefit from our many years of experience with our own studies and our know-how in dealing with ophthalmic instrumentation as well as our numerous contacts and cooperation partners in the field of ophthalmology.
Development of protocols for clinical data acquisition and analysis
Training of the clinic(s) for prototype tests and monitoring of implementation
Analysis, plausibility check, preparation and presentation of your study data