novineon CRO is a leading service provider for research and regulatory affairs. For two decades we have been supporting manufacturers of medical devices and in-vitro diagnostics (IVD) in clinical and regulatory affairs related to conformity issues, e.g. clinical evaluation and clinical trials.
Demands on the performance of medical devices and medical procedures are continuously increasing. Collaboration with a CRO (contract research organization) can be a decisive competitive advantage in that it minimizes the need for research and exposure to regulatory issues.
Together with you, we develop individual and practical solutions for biological evaluation, risk analysis, performance evaluation for IVDs, PMCF/PMS as well as product registration in non-European markets. We cooperate with a team of consultants consisting of recognized clinical specialists and thus offer expertise in the entire range of medical devices.
Our long-standing customers appreciate our proven and documented methods. We are certified according to ISO 9001.
Medical technology and diagnostic equipment offer new possibilities to improve people's health and quality of life. Research-intensive companies have excellent opportunities to win market share. novineon CRO helps to ensure that effective and safe products find the best possible way into clinical application.
In our work, we focus entirely on the needs of our customers and business partners. Therefore our work is characterized by care, speed and creativity. We attach great importance to a personal and trusting relationship with our customers, which is why you will be looked after individually by members of our team.
The skills and motivation of our team are an important asset for us. We respect their interests, talents and ideas. This has enabled us to build up a broad knowledge in the last 20 years and to continuously improve our methods.