novineon CRO supports your medical device through all phases of its life cycle:  from usability and clinical evaluation to post-market surveillance and to the next round with your enhanced successor product.

novineon CRO offers services for technical documentation. Whether the performance evaluation of your in vitro diagnostic medical devices, review of the risk analysis and instructions for use or the preparation of the plan and report of the performance evaluation and post-market surveillance, novineon has the right solution.