Outsource your company’s MDR/IVDR updates to us. We take care of the technical documentation and the necessary updates to your quality management system. The regulatory environment is changing rapidly, and the demands for manufacturers, distributors and importers are increasing.
Our team always uses the latest information to update your quality management system and technical documentation. We also share our competence to our clients through training.
In the EU, the most significant changes for medical devices are related to the implementation of the MD and IVD regulations. The transitional period is still ongoing, but the system updates should be considered in advance so that you have time to complete the changes in time.