Solnovis is your competent consultant in the area of Regulatory Affairs and Quality Management in each project phase. We combine wide experience in the field of medical technology with sound consulting competence.
Several steps are necessary for the launch of medical devices. The requirements depend on the target market and the local regulatory and standards requirements. We support your certification process (CE, US and international) and help you to prepare for external and internal Audits.
Our solution-based strategies enable a cost-effective, efficient and prompt realisation of the particular project.