Development Services & Consulting
Qvanteq is offering its know-how for development projects as well as in consulting mandates.
Qvanteq provides general support for your development program. Based on our technical expertise as well as from our experience in developing a class III medical device (including clinical study) we can support your project in the following areas: quality, regulatory (incl. MDR), validation (packaging, sterilization, manufacturing processes), manufacturing, engineering and project management.
Development of / development support for your medical device including also planning and execution of animal studies and regulatory approval.
In vitro testing using whole human blood / endothelial cells
Support and execution of your thrombogenicity assessment of novel materials, surfaces or entire devices including also flow induced shear stress. We have a range of test systems: screening assays for larger number of samples, blood flow loop setup and others.
Contact Qvanteq to learn more about how we can help you.