About us
Eurofins Medical Device Consulting is at your disposal with the highest level of scientific consulting expertise in the testing of medical devices. From the market launch to the re-evaluation of existing products.
We offer you solutions and strategic approaches for complex toxicological or regulatory problems. Requirements change quickly, we are always up to date and our regulatory expertise in global markets brings orientation to your process.
You can make more effective use of time and costs and thus achieve the best possible results through our advice from the start of your entire product development. We provide expert opinions, carry out a risk assessment for your product and support you in planning your test strategy.
Eurofins Sterile Packaging - steripac & inpac , are our concept, production and validation partners for cleaning, assembly, packaging and sterilization of your medical devices with modern cleanrooms of ISO classes 7 and 8. We accompany you in the development from non-sterile to sterile, ready-for-sale product and realize any number of pieces.
Eurofins Medical Device Testing - test laboratories for safe medical devices
With 16 laboratories in Europe, North America and the Asia-Pacific region, the experts at Eurofins Medical Device Testing offer their customers from all over the world comprehensive expertise and a full range of services in accordance with the requirements of GMP, GLP and ISO 17025 for the testing of medical devices.
From chemical characterization of degradation products and extractables and solubilities testing to toxicological risk assessments and biological evaluations, Eurofins Medical Device Testing can perform the appropriate testing required to best support your international medical device regulatory submissions.